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Myokine

Myokines are cytokines and peptides produced, expressed, and released by cells (myocytes) in response to muscular contractions or exercise, functioning as signaling molecules with autocrine, paracrine, and endocrine effects that mediate communication between and other organs. The term "myokine" was first coined in 2003 by exercise physiologist Bengt Saltin to describe these muscle-derived factors, building on the 1997 discovery of as the inaugural myokine by Se-Jin Lee and colleagues, which inhibits muscle growth. Over 600 myokines have since been identified through secretome analyses of human myocyte cultures, highlighting 's role as an endocrine organ. These molecules are synthesized via transcriptional and translational processes triggered by mechanical stress from contractions, enabling rapid release into circulation to influence distant tissues. Key functions of myokines include regulating mass and function by promoting hypertrophy, proliferation, and differentiation while counteracting atrophy; they also modulate , inflammation, and tissue regeneration across the body. Through inter-organ crosstalk, myokines affect (e.g., inducing lipolysis and fat browning), the liver (e.g., enhancing ), (e.g., stimulating formation), the (e.g., supporting neurogenesis), and the vascular system (e.g., improving endothelial function). Notable examples include interleukin-6 (IL-6), which boosts fat oxidation and insulin sensitivity while exerting anti-inflammatory effects; irisin, which converts to energy-expending brown fat; , which enhances cognitive function and ; and myostatin, which limits muscle growth to prevent excessive hypertrophy. Dysregulation of myokine signaling is implicated in conditions like sarcopenia, , and metabolic disorders, underscoring their therapeutic potential in exercise-based interventions.

Discovery and History

Initial Identification of Muscle-Derived Factors

Myokines are defined as cytokines or hormones that are produced and released by cells, known as myocytes, primarily in response to . This secretion enables to act as an endocrine organ, influencing systemic physiological processes beyond local muscle function. The discovery of myokines began with the identification of in 1997 by McPherron et al. and Se-Jin Lee, a member of the (TGF-β) superfamily that acts as a negative regulator of growth, marking it as the first recognized myokine. During the and early 2000s, researchers began to recognize 's role as an endocrine organ through observations that muscle-derived factors enhance in peripheral tissues and promote fat metabolism during exercise. These early insights stemmed from studies showing that physical activity improves insulin sensitivity and lipid oxidation, suggesting the involvement of humoral signals from contracting muscle. The foundational shift occurred with the demonstration that actively secretes signaling molecules akin to those from traditional endocrine glands. A pivotal experiment in 2000 by Pedersen and colleagues directly identified interleukin-6 (IL-6) as the first muscle-derived factor secreted during in humans. In their study, IL-6 mRNA expression and protein release were measured in biopsies before and after prolonged exercise, revealing a marked increase in circulating IL-6 levels attributable to production within contracting myocytes. This work established IL-6 as the inaugural exercise-induced myokine, with human exercise trials confirming its release specifically from to support . Subsequent analyses indicated that IL-6 is primarily released via from myocytes, while other early-recognized factors may involve membrane shedding for proteolytic liberation. These findings laid the groundwork for viewing as a trigger for endocrine-like signaling.

Key Milestones and Research Evolution

The concept of myokines gained significant traction in 2012 with the identification of irisin, a muscle-derived that promotes the browning of , thereby linking activity to systemic metabolic regulation. This discovery, reported by Boström et al., marked a pivotal shift toward recognizing myokines as key mediators in inter-tissue communication, building on earlier observations of muscle-secreted factors like IL-6 identified in 2000. By 2014, research had formalized the paradigm of muscle-organ crosstalk, with studies demonstrating how exercise-induced myokines facilitate signaling between and distant organs such as the liver, , and to influence metabolic . Over the subsequent decade, myokine research evolved from a primary emphasis on exercise-stimulated —initially highlighted in seminal works defining myokines in 2003—to broader investigations into their under resting conditions and in pathological states. This progression revealed myokines' roles beyond acute , including chronic dysregulation in metabolic disorders, where altered profiles contribute to progression rather than solely beneficial adaptations. Recent bibliometric analyses from 2023 to 2025 underscore emerging trends, with heightened focus on myokines in , where they modulate pathways; , via anti-inflammatory and insulin-sensitizing effects; and cancer, particularly models involving tumor-muscle interactions. In 2024, a synthesized evidence on myokines' influence on bone metabolism, highlighting their anabolic effects on osteoblasts and potential therapeutic implications for through exercise-mimetic interventions. This built momentum into 2025, when a comprehensive review proposed the "Myokine-mediated Multi-organ " theory, positing myokines as central hubs in a dynamic web of endocrine signaling that coordinates metabolic flux across organs like the heart, liver, and during and . Addressing prior research gaps, studies from 2023 onward have expanded investigations into how myokines from influence cardiac protection, such as against ischemia-reperfusion injury via factors like myonectin, and vascular function, including endothelial and prevention. This interdisciplinary broadening promises to refine therapeutic strategies targeting myokine networks in multifaceted diseases.

Secretion and Regulation

Mechanisms of Myokine Secretion

Myokines are primarily triggered for secretion through repetitive contractions during physical exercise, which initiate intracellular signaling cascades leading to altered . These contractions stimulate the activation of transcription factors, notably peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α), a master regulator of and metabolic adaptation in muscle fibers. PGC-1α binds to promoters of myokine-encoding genes, promoting their transcription without being secreted itself. At the molecular level, muscle contractions elevate intracellular calcium levels, which activate signaling pathways including (AMPK). This calcium-AMPK axis, often in concert with PGC-1α, upregulates the expression of specific myokine genes, such as fibronectin type III domain-containing protein 5 (), the precursor to irisin. For instance, AMPK is essential for maintaining FNDC5 expression in , ensuring sustained myokine production in response to contractile stress. Myokines are released via diverse secretion pathways tailored to their molecular structure. Larger myokines, such as interleukin-6 (IL-6), are typically exported through the classical route, involving synthesis in the , processing in the Golgi apparatus, and vesicular fusion with the plasma membrane. Alternative non-classical pathways include encapsulation within exosomes—small extracellular vesicles (30–150 nm) shed from s—that transport myokines like irisin and IL-15 to distant tissues, with exosome release amplified by acute exercise bouts. Additionally, certain myokines arise from membrane-bound precursors through proteolytic shedding; for example, irisin is generated by enzymatic cleavage of the transmembrane protein on the muscle cell surface. The secretion of myokines exhibits dose-dependency on exercise intensity, where higher workloads elicit proportionally greater release to meet metabolic demands. Even in the absence of exercise, skeletal muscle maintains basal myokine secretion at low levels to support tissue homeostasis, including regulation of local inflammation and energy balance.

Factors Influencing Secretion

The secretion of myokines is profoundly influenced by exercise parameters, with distinct profiles emerging from aerobic versus resistance training modalities. Aerobic exercise, such as endurance activities, acutely elevates interleukin-6 (IL-6) levels up to 100-fold post-exercise, serving as an energy sensor to enhance glucose uptake and fat oxidation. In contrast, resistance training promotes the release of immunoregulatory myokines like interleukin-15 (IL-15) and myonectin, supporting muscle hypertrophy and repair. Acute bouts of exercise trigger rapid increases in IL-6 and meteorin-like protein (Metrnl), while chronic training sustains elevated levels of myonectin and brain-derived neurotrophic factor (BDNF), leading to adaptive improvements in metabolic health. Non-exercise factors also modulate myokine production, including , , , and . Aging is associated with diminished secretion of beneficial myokines such as IL-15 and irisin, contributing to reduced muscle regenerative capacity in conditions like . Sex differences arise through hormonal influences, with testosterone in males inhibiting release to favor muscle . Chronic inflammation shifts myokine profiles toward catabolic states, elevating while suppressing factors. Pathological conditions further alter myokine secretion, often impairing beneficial profiles. In , irisin levels are reduced and proinflammatory myokines are dysregulated, exacerbating and adipose . Sedentary lifestyles diminish the release of protective myokines like IL-6 and irisin, fostering a pro-inflammatory and . Conversely, training-adapted muscle in active individuals shows enhanced myokine output, mitigating these deficits. Recent from a 2025 randomized demonstrates that 36 weeks of personalized resistance training in older women with possible sarcopenic obesity significantly increased circulating insulin-like growth factor-1 (IGF-1) by 7.73 ng/mL and decreased by 0.49 ng/mL, alongside improvements in muscle strength and function. Hormonal regulators exert direct control over myokine dynamics, integrating endocrine signals with muscle responses. Insulin enhances in muscle while suppressing proinflammatory myokine release, thereby supporting anabolic processes. Elevated , as in stress states, upregulates to promote muscle and .

Physiological Functions

Metabolic and Endocrine Regulation

Myokines function as endocrine signals secreted by skeletal muscle to regulate systemic , including the promotion of in skeletal muscle and peripheral tissues. For instance, interleukin-6 (IL-6), a prototypical myokine released during exercise, enhances glucose disposal by stimulating (AMPK) pathways, thereby improving insulin-independent in muscle cells. Irisin, another key myokine, similarly boosts while inducing in , contributing to better . These actions help maintain euglycemia during and in resting states. In addition to glucose regulation, myokines drive lipolysis and the browning of white adipose tissue (WAT), transforming energy-storing white adipocytes into thermogenic beige adipocytes that increase energy expenditure. Irisin, derived from fibronectin type III domain-containing protein 5 (FNDC5), activates uncoupling protein 1 (UCP1) expression in WAT, promoting mitochondrial biogenesis and fat oxidation to counteract obesity. This process exemplifies muscle-fat crosstalk, where myokines like irisin and IL-6 reduce adiposity by inhibiting white fat accumulation and enhancing lipid mobilization. Recent 2024 analyses highlight myokines' anti-diabetic potential in obesity trends, showing that exercise-induced elevations in IL-6 and irisin improve insulin sensitivity and mitigate type 2 diabetes risk through these mechanisms. Myokines also influence insulin sensitivity and across organs, fostering adaptive metabolic responses. For example, IL-6 signaling during exercise enhances fat oxidation in muscle and liver by activating AMPK, which suppresses hepatic and promotes utilization, preventing excessive glucose release. Paracrine effects on adjacent adipocytes further amplify this by increasing lipolytic activity, while endocrine actions extend to distant sites like the liver to regulate energy partitioning. Collectively, these pathways underscore myokines' role in integrating muscle-derived signals for whole-body metabolic balance and endocrine harmony.

Cardiovascular and Musculoskeletal Effects

Myokines play a crucial role in regulating cardiac structure and by mitigating pathological remodeling processes. Certain myokines exert protective effects against cardiac and , key contributors to heart failure progression. For instance, they inhibit the development of in cardiomyocytes and reduce fibrotic deposition in the myocardium, thereby preserving ventricular during stress conditions such as ischemia. Additionally, myokines promote in cardiac tissue, enhancing vascularization and oxygen supply to support myocardial repair and adaptation to exercise-induced demands. In the context of heart regulation, , a myokine secreted by in response to exercise, facilitates collagen organization within cardiac . By modulating fibril assembly and stabilizing the matrix, decorin prevents excessive and supports proper tissue remodeling post-injury, such as . This anti-fibrotic action involves inhibition of transforming growth factor-beta (TGF-β) signaling, which otherwise drives overproduction and scar formation. Autocrine effects of myokines on cardiomyocytes further contribute to these benefits, enabling local metabolic regulation and protection against adverse remodeling directly within heart muscle cells. Shifting to musculoskeletal impacts, myokines help maintain muscle integrity by inhibiting wasting processes, particularly under conditions of disuse or . They counteract through pathways that promote protein synthesis and cell activation, ensuring mass preservation and functional recovery. In bone tissue, myokines stimulate activity, fostering bone formation and enhancing overall density. This anabolic influence counters resorption, supporting structural integrity and reducing risk via increased mineralization and matrix deposition. Recent 2024 research highlights advances in understanding myokine-driven , emphasizing their role in exercise-mediated and bone mass augmentation. Studies demonstrate that myokine secretion during correlates with 1-2% improvements in after structured training regimens, underscoring their therapeutic potential for maintaining skeletal health. from myokines to osteocytes further amplifies these effects, coordinating cellular responses that optimize and adaptation to mechanical loads.

Neurological and Immunomodulatory Roles

Myokines exert significant influence on neurological function through endocrine signaling pathways that enable certain molecules to cross the , thereby promoting and cognitive processes. For instance, exercise-induced myokines such as irisin and (BDNF) traverse the BBB to enhance in regions like the , facilitating neuronal adaptation and connectivity. This supports by activating signaling cascades, including the /PKA/CREB pathway, which strengthens and information retention in the brain. Additionally, muscle-derived BDNF directly contributes to hippocampal , increasing proliferation in the and counteracting age-related cognitive decline. These effects extend to mood regulation, where elevated BDNF levels mitigate depressive symptoms by modulating systems and reducing . Beyond , myokines participate in regulation via endocrine signaling to the , a key integrator of circadian rhythms and homeostatic balance. triggers myokine release that influences hypothalamic nuclei, promoting restorative patterns and alleviating disruptions associated with sedentary lifestyles. This hypothalamic modulation underscores the broader muscle-brain , where myokines like IL-6 and BDNF act as intermediaries to synchronize neural activity with peripheral metabolic demands, enhancing overall brain resilience. In the realm of , myokines exhibit properties by balancing pro- and cytokines, thereby mitigating excessive immune responses. Interleukin-6 (IL-6), a prototypical myokine, demonstrates a : during acute exercise, it promotes an milieu by stimulating the release of IL-10 and other suppressors, which dampen without promoting tissue damage. In contrast, chronic elevation of IL-6, often linked to inactivity, can exacerbate pro-inflammatory states by sustaining cytokine storms. This balance is crucial for maintaining immune , as myokines like IL-6 and IL-15 regulate the and of immune cells. Mechanistically, myokines facilitate paracrine modulation of T-cells and macrophages within the muscle microenvironment, directing immune cell trafficking and function to support resolution of . For example, exercise-induced myokines attract macrophages to sites of microdamage, shifting them from pro-inflammatory to anti-inflammatory phenotypes, which aids in tissue repair and prevents chronic immune activation. Similarly, they influence T-cell recruitment by altering gradients, ensuring targeted immune surveillance without overactivation. Through these paracrine interactions, myokines integrate local immune responses with systemic endocrine signals, fostering an adaptive immunomodulatory network.

Emerging Roles in Organ Crosstalk

Myokines play a pivotal role in the interorgan network, particularly through the muscle-liver axis, where they regulate hepatic to maintain during . For instance, exercise-induced myokines such as interleukin-6 (IL-6) signal to the liver to enhance glucose output, counterbalancing increased muscular and preventing . Similarly, in the muscle-kidney axis, myokines like irisin and IL-6 mediate renal protection by suppressing metabolic reprogramming and in damaged kidneys, thereby preserving renal function under stress conditions. Recent developments have advanced the understanding of myokine functions, including the 2025 proposal of the "Myokine-mediated Multi-organ Metabolic Network" theory, which posits that myokines orchestrate dynamic inter-organ communication to sustain metabolic balance across tissues. This theory highlights how myokines integrate signals from multiple organs, influencing systemic energy distribution and to physiological demands. Additionally, myokine exosomes facilitate long-range signaling by encapsulating bioactive molecules for targeted to distant organs, enabling sustained endocrine effects beyond direct secretion. Specific crosstalk mechanisms include myokine interactions with the , where factors like and irisin protect beta-cell function by mitigating and enhancing insulin secretion in response to metabolic challenges. In the gut-muscle axis, myokines modulate the by promoting beneficial microbial shifts through exercise, which in turn influences muscle via short-chain production and reduced . Bidirectional signaling further underscores myokine involvement in organ crosstalk, as adipokines from can reciprocally regulate myokine release from , amplifying anti-inflammatory and metabolic effects across the endocrine network. This interplay ensures coordinated responses to maintain , with examples like modulating IL-6 production in muscle to fine-tune energy partitioning.

Specific Myokines

Myostatin

Myostatin, also known as growth differentiation factor 8 (GDF8), is a secreted protein belonging to the transforming growth factor-beta (TGF-β) superfamily, primarily produced by cells. It is synthesized as a precursor protein that undergoes proteolytic processing to form the mature, active dimer, which circulates as a myokine to exert autocrine and paracrine effects. Exercise, particularly aerobic and , suppresses secretion and reduces its circulating levels, thereby alleviating its inhibitory influence on muscle growth. As a potent negative regulator, primarily functions to limit by inhibiting myoblast and through of the Smad2/3 signaling pathway. In the cardiac context, contributes to remodeling processes by modulating cardiomyocyte growth and , potentially preventing excessive under stress conditions. Loss-of-function mutations in the myostatin gene lead to pronounced muscle overgrowth, as exemplified by the double-muscling phenotype in cattle, where a 11-base pair deletion in the coding region disrupts protein function and results in up to 20% increased muscle mass. This discovery has inspired therapeutic strategies targeting myostatin inhibition for muscular dystrophies, such as , where monoclonal antibodies and gene therapies have shown promise in preclinical models by enhancing muscle mass and strength, though clinical trials have faced challenges in efficacy translation. Dysregulation of , characterized by elevated circulating levels, is implicated in , where it correlates with reduced muscle mass and function in older adults. Recent 2025 studies have further positioned as a potential for risk, with higher levels independently associated with disease prevalence and progression in cohorts including patients. This elevation may be antagonized by , highlighting 's role in muscle .

Interleukin Family

The interleukins represent a key family of cytokines that function as myokines, primarily secreted by cells in response to during physical exercise. Among these, interleukin-6 (IL-6) is recognized as the prototypical myokine, with its expression and release markedly upregulated in during aerobic and resistance activities. This secretion occurs independently of immune cell activation, distinguishing exercise-induced IL-6 from its inflammatory roles in other contexts. IL-6 exerts beneficial metabolic effects by promoting in and enhancing in muscle, thereby facilitating energy mobilization during prolonged exercise. It also displays properties, counteracting pro-inflammatory cytokines like tumor necrosis factor-alpha (TNF-α) and stimulating the production of anti-inflammatory mediators such as interleukin-10 (IL-10). In parallel, interleukin-15 (IL-15), another prominent member of this family, supports by enhancing protein synthesis and inhibiting , contributing to adaptive responses in following resistance training. A hallmark of IL-6 as a myokine is its rapid and substantial elevation in levels, which can increase up to 100-fold immediately following intense exercise, before returning to baseline within hours. Recent 2025 research has further highlighted IL-6's potential in cancer suppression, demonstrating that exercise-induced elevations in IL-6 levels, as part of broader myokine responses, correlate with reduced tumor in vitro, suggesting synergies with therapeutic modalities like radiotherapy. At the molecular level, myokines such as IL-6 and IL-15 primarily signal through the Janus kinase-signal transducer and activator of transcription (JAK-) pathway. Upon binding to their respective receptors on target cells, these ligands activate receptor-associated JAK kinases, leading to and nuclear translocation of STAT proteins, which then regulate involved in metabolic and anabolic processes. This pathway underscores the endocrine-like communication of muscle-derived to distant tissues.

Irisin

Irisin is a myokine produced through the proteolytic cleavage of , a type I transmembrane precursor protein predominantly expressed in . The mature consists of approximately 112 , forming a structure with a type III domain that enables its into circulation following enzymatic processing by proteases such as . Its is regulated by coactivator 1-alpha (PGC-1α) in response to exercise stimuli. Discovered in 2012, irisin was initially identified in mice as an exercise-induced factor derived from that mimics some metabolic benefits of physical activity. Early reports suggested its role in promoting metabolic adaptations, but controversy arose regarding its existence and physiological relevance in humans, primarily due to challenges in detecting low circulating levels and concerns over specificity in immunoassays. This debate was largely resolved by 2019 studies employing and validated assays, which confirmed detectable irisin in human and , with levels influenced by age and sex. The primary function of irisin centers on metabolic adaptation, particularly by inducing the "browning" of , where it drives the differentiation of white adipocytes into fat cells capable of . This process enhances energy expenditure and fat oxidation, as irisin directly activates uncoupling protein 1 (UCP1) in adipocytes, uncoupling mitochondrial respiration from ATP production to generate heat. Additionally, irisin improves insulin sensitivity by facilitating in and , thereby mitigating associated with sedentary lifestyles. Exercise acutely elevates circulating irisin levels, with the rise correlating positively with increased resting energy expenditure and overall metabolic rate in humans. In 2024 research, recombinant irisin administration in high-fat diet-fed mice reversed obesity-related metabolic dysfunction, including reduced body weight and improved glucose , through enhanced activation. These findings underscore irisin's potential as a mediator of exercise-induced metabolic benefits.

Brain-Derived Neurotrophic Factor (BDNF)

(BDNF) serves as a key myokine secreted by , primarily in its precursor pro-BDNF form, which differs from the mature BDNF isoform predominantly produced in the brain. This muscle-derived pro-BDNF is expressed at high levels in human type I muscle fibers and is significantly upregulated during acute and chronic exercise, with contractions inducing its local release within muscle tissue to support neuromuscular adaptations. Unlike brain-derived mature BDNF, which circulates more readily, pro-BDNF from muscle exhibits limited systemic release but can influence peripheral and functions through endocrine signaling. As a myokine, BDNF promotes neuronal by enhancing the viability of neurons in response to and , while also driving through mechanisms that strengthen connections between neurons, particularly in regions involved in learning and memory. In the context of mood stabilization, elevated BDNF levels counteract depressive states by modulating systems and reducing , thereby fostering resilience against mood disorders. These functions are especially relevant in exercise-induced scenarios, where muscle-derived BDNF contributes to and cognitive benefits. Exercise-mediated increases in BDNF have been linked to a reduced risk of depression, as physical activity elevates circulating and tissue BDNF levels, correlating with improved mood and lower incidence of depressive symptoms in both healthy individuals and those with mood disorders. Recent 2023 studies further highlight BDNF's role in sleep regulation, demonstrating that altered BDNF expression disrupts slow-wave sleep and contributes to insomnia, while exercise-induced BDNF may restore sleep architecture by enhancing hippocampal activity. The primary mechanism underlying these effects involves activation of the TrkB receptor in the hippocampus, where BDNF binding triggers downstream signaling cascades, including phosphorylation of CREB and enhancement of long-term potentiation, essential for neuroplasticity and emotional regulation.

Decorin

Decorin is a small leucine-rich (SLRP) that functions as an exercise-induced myokine secreted by cells during contraction. As part of the SLRP family, it consists of a core protein with attached chains, enabling its interactions with components and signaling molecules. In tissue remodeling, plays a key role in regulating assembly by promoting fibrillogenesis and organizing fibers in the . This function is mediated through direct binding to type I and sequestration of transforming growth factor-β (TGF-β), which inhibits excessive production and . By modulating TGF-β signaling, helps maintain structured tissue architecture, particularly in response to mechanical stress from muscle activity. Decorin also exhibits anti-cancer properties by inhibiting tumor growth through interference with epidermal growth factor receptor () signaling. It binds to , attenuating downstream pathways such as ERK that promote and survival in tumor cells. This suppression extends to invasion and , as demonstrated in models of and cancers where decorin overexpression reduced tumor progression. A 2025 study on survivors found that a single bout of or high-intensity interval training acutely increased circulating decorin levels, which in turn suppressed proliferation of MDA-MB-231 cancer cells by up to 30%. Additionally, decorin contributes to cardiovascular matrix stability by similar ECM regulatory mechanisms.

SPARC (Osteonectin)

SPARC, also known as osteonectin or secreted protein acidic and rich in , is a matricellular expressed in various tissues, including , where it functions as an exercise-inducible myokine. Its secretion from muscle cells increases in response to acute and chronic exercise, contributing to tissue remodeling processes. As a key component of the (ECM), SPARC plays a central role in bone-muscle crosstalk by influencing matrix assembly and cellular interactions at the osteo-muscular . In bone metabolism, SPARC modulates mineralization by regulating the deposition and organization of mineralized ECM, particularly through its high affinity for calcium and . It promotes differentiation and bone formation while inhibiting excessive matrix calcification, thereby maintaining skeletal integrity. Recent 2024 research using multi-omics approaches has identified SPARC as a conserved osteokine secreted by s, highlighting its role in promoting bone formation and noting that its expression declines with aging, potentially exacerbating bone mass loss. Additionally, SPARC supports within and muscle tissues by modulating (VEGF) signaling, which facilitates nutrient delivery and tissue repair during exercise-induced adaptations. Mechanistically, interacts directly with , acting as a chaperone to facilitate proper assembly and prevent premature collagen interactions with cell surfaces, which is essential for organized in and muscle. It also binds VEGF, thereby fine-tuning angiogenic responses to ensure balanced vascularization without excessive proliferation in mineralizing environments. These interactions underscore SPARC's protective role against pathological ECM remodeling, such as in cardiac contexts indirectly linked to musculoskeletal , by preserving matrix compliance and endothelial integrity.

Follistatin and Other Emerging Myokines

, a secreted produced by cells, acts as a potent to , a member of the transforming growth factor-β (TGF-β) superfamily that inhibits muscle growth. By binding directly to myostatin, follistatin neutralizes its inhibitory effects on and , thereby promoting and increasing muscle mass. This antagonistic interaction has been demonstrated in preclinical models where follistatin overexpression leads to significant muscle enlargement independent of myostatin levels in some contexts. Additionally, follistatin binds with high affinity to activins, other TGF-β family members, inhibiting their interaction with receptors and suppressing downstream signaling pathways that limit muscle development. As of 2025, studies have highlighted follistatin's potential as a biomarker for sarcopenia, with higher serum levels associated with physical functional impairment and disease severity in conditions like rheumatoid arthritis in aging populations. In multiorgan networks, follistatin contributes to endocrine signaling that coordinates muscle-liver and muscle-adipose interactions, influencing systemic metabolism and tissue remodeling. Among emerging myokines identified between 2023 and 2025, fibroblast growth factor 21 (FGF21) stands out for its involvement in the metabolic stress response. Secreted by skeletal muscle under conditions like endoplasmic reticulum stress or psychological strain, FGF21 acts as an endocrine signal to enhance glucose uptake, promote fatty acid oxidation, and protect against insulin resistance. This myokine's production surges in response to exercise or nutritional challenges, facilitating adaptations in distant organs such as the liver and adipose tissue. Meteorin-like protein (Metrnl), another recently characterized myokine, exerts neuroprotective effects and drives browning. Induced in muscle by , Metrnl circulates to stimulate neuronal survival pathways in the , reducing and supporting cognitive function during aging or neurodegenerative stress. Concurrently, it promotes the conversion of to beige fat, increasing and energy expenditure via endocrine signaling that activates uncoupling protein 1 in adipocytes. These actions position Metrnl as a key player in muscle-brain and muscle-adipose within evolving multiorgan frameworks.

Clinical and Therapeutic Implications

Myokines in Sarcopenia and Aging

, characterized by progressive loss of mass and function, is closely linked to alterations in myokine secretion during aging. Declining levels of beneficial myokines such as irisin and contribute to this by impairing muscle regeneration and promoting . Irisin, derived from fibronectin type III domain-containing protein 5 (), decreases in mRNA and protein expression with advancing age, exacerbating muscle wasting and metabolic dysfunction in aged models. Similarly, serum concentrations diminish over time, reducing its antagonistic effect on and thereby accelerating sarcopenic progression. In contrast, pro-atrophic myokines like often elevate in sarcopenic individuals, further disrupting muscle . Interleukin-15 (IL-15), another key myokine, shows reduced plasma levels in older adults with , correlating with diminished muscle strength and increased risk of frailty. Exercise interventions effectively counteract by stimulating myokine release to preserve muscle mass and function. , particularly resistance training, upregulates secretion of anabolic myokines such as irisin, , and IL-15, which enhance and mitigate inflammatory pathways. A 2025 randomized controlled trial demonstrated that 36 weeks of personalized resistance training in older women with possible sarcopenic significantly improved muscle function and elevated circulating myokine levels, including irisin and IL-6, leading to better and reduced fat mass. These findings underscore exercise's role in restoring myokine balance, with resistance protocols showing dose-dependent benefits on physical performance in sarcopenic populations. Myostatin inhibition emerges as a promising anti-aging therapeutic target for , given its role in limiting muscle growth. Pharmacological blockade of , such as with anti-myostatin antibodies, has reversed age-related muscle loss in preclinical models by increasing muscle mass and strength without adverse effects on other tissues. Clinical translation of this approach is ongoing, supported by evidence that levels rise in chronic aging conditions, making it a viable intervention to halt sarcopenic decline. In clinical contexts, myokines serve as biomarkers for sarcopenia detection and monitoring. A 2025 review highlights four key myokines—myostatin, irisin, follistatin, and BDNF—as potential diagnostic tools, with their dysregulated profiles reflecting muscle wasting severity in older adults. Low IL-15 levels, in particular, predict risk in community-dwelling elderly, offering a non-invasive marker for early intervention. These biomarkers enable personalized assessments, guiding therapies like exercise or inhibitors to improve outcomes in aging populations.

Applications in Metabolic Disorders and Cancer

Myokines have emerged as promising therapeutic targets in metabolic disorders, particularly and , due to their roles in interorgan crosstalk that regulates and insulin sensitivity. In , exercise-induced myokines such as irisin facilitate the browning of , promoting and fat oxidation, which contributes to and improved metabolic profiles. Recent bibliometric analyses from 2024 highlight a surge in research on myokines like irisin and interleukin-6 (IL-6), emphasizing their mediation of muscle-adipose interactions to combat -related and enhance interorgan health, with publication volumes increasing 12.5-fold since the prior decade. For , myokine mimetics, including synthetic analogs of irisin and (BDNF), have shown potential to enhance and mitochondrial function in preclinical models, mimicking exercise benefits to improve . Exercise protocols specifically designed to boost irisin levels offer a non-pharmacological approach to weight management in metabolic disorders. High-intensity interval training (HIIT) has been demonstrated to elevate circulating irisin more effectively than moderate continuous exercise, leading to greater reductions in body fat and improvements in insulin sensitivity in obese individuals. Long-term moderate aerobic exercise also significantly increases irisin in both obese and healthy populations, correlating with sustained weight loss and metabolic improvements over months. These protocols underscore irisin's role as a key myokine linking physical activity to adipose tissue remodeling and glycemic control. In , certain myokines exhibit anti-tumor effects by modulating the and immune responses. IL-6, when secreted by exercising muscle, can induce and inhibit in specific subtypes, contrasting its pro-inflammatory role in other contexts. , another muscle-derived myokine, suppresses tumor growth by inhibiting (EGFR) signaling, reducing , and preventing epithelial-mesenchymal transition in various cancer models. Emerging 2025 studies on exercise interventions in survivors reveal that myokine elevation, particularly through HIIT or resistance , suppresses tumor cell growth in survivors. Therapeutic strategies targeting hold promise for managing , a severe muscle-wasting affecting up to 80% of advanced cancer patients. inhibitors, such as monoclonal antibodies like bimagrumab, preserve muscle mass and improve physical function in preclinical cancer models by blocking the TGF-β pathway that drives . Clinical trials have explored these agents to counteract in pancreatic and lung cancers, showing modest gains in without exacerbating tumor progression. Despite these advances, translating myokine-based therapies faces significant challenges, including delivery methods and specificity in clinical trials. Protein-based myokines suffer from short half-lives, proteolytic , and off-target effects due to ubiquitous receptors, complicating targeted to muscle or adipose tissues. Strategies like and encapsulation aim to improve stability and tissue specificity, but trials often encounter and dosing inconsistencies, limiting efficacy in heterogeneous patient populations. Ongoing research emphasizes the need for precise biomarkers to monitor myokine responses and refine trial designs for metabolic and oncologic applications.