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Identification of human exercise-induced myokines using secretome analysis
Milène Catoire1, Marco Mensink, Eric Kalkhoven
1Nutrition, Metabolism and Genomics Group, Division of Human Nutrition, Wageningen University, Wageningen, the Netherlands;
Physiological Genomics
|February 13, 2014
Summary
This study identified CX3CL1 (fractalkine) and CCL2 (MCP-1) as novel myokines induced by acute endurance exercise. These signaling proteins, released by muscles, may play a role in inter-organ communication.
Area of Science:
- Exercise physiology
- Molecular biology
- Endocrinology
Background:
- Endurance exercise improves cardio-metabolic health.
- Myokines, muscle-derived cytokines, are implicated but poorly understood in acute exercise.
- Limited data exists on human myokine responses to acute endurance exercise.
Purpose of the Study:
- Identify novel exercise-induced myokines in humans.
- Investigate myokine changes following acute and training-based endurance exercise.
- Determine if identified myokines are present in circulation.
Main Methods:
- One-legged acute endurance exercise (1 hour) in 12 males.
- 12-week exercise training intervention in 18 males.
- Microarray analysis of muscle secretome, followed by ELISA/multiplex assays for plasma validation.
Main Results:
- Acute exercise revealed 86 putative myokines, with CX3CL1 (fractalkine) and CCL2 (MCP-1) increasing at mRNA and plasma levels.
- Known myokines IL-6 and FGF 21 changed at mRNA but not plasma levels post-acute exercise.
- Exercise training identified 69 putative myokines, with limited overlap (13 genes) compared to acute exercise.
Conclusions:
- CX3CL1 and CCL2 are identified as myokines induced by acute exercise at both gene and protein levels.
- These novel myokines may mediate communication between skeletal muscle and other organs.
- Acute exercise responses differ significantly from chronic training adaptations in myokine profiles.

