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Neuregulins mediate calcium-induced glucose transport during muscle contraction
- Source :
- The Journal of biological chemistry. 281(31)
- Publication Year :
- 2006
-
Abstract
- Neuregulin, a growth factor involved in myogenesis, has rapid effects on muscle metabolism. In a manner analogous to insulin and exercise, neuregulins stimulate glucose transport through recruitment of glucose transporters to surface membranes in skeletal muscle. Like muscle contraction, neuregulins have additive effects with insulin on glucose uptake. Therefore, we examined whether neuregulins are involved in the mechanism by which muscle contraction regulates glucose transport. We show that caffeine-induced increases in cytosolic Ca2+ mediate a metalloproteinase-dependent release of neuregulins, which stimulates tyrosine phosphorylation of ErbB4 receptors. Activation of ErbB4 is necessary for Ca2+-derived effects on glucose transport. Furthermore, blockage of ErbB4 abruptly impairs contraction-induced glucose uptake in slow twitch muscle fibers, and to a lesser extent, in fast twitch muscle fibers. In conclusion, we provide evidence that contraction-induced activation of neuregulin receptors is necessary for the stimulation of glucose transport and a key element of energetic metabolism during muscle contraction.
- Subjects :
- Male
medicine.medical_specialty
Receptor, ErbB-4
Glucose uptake
Biology
In Vitro Techniques
Biochemistry
Cytosol
Internal medicine
Caffeine
medicine
Animals
Phosphorylation
Rats, Wistar
Molecular Biology
ERBB4
Neuregulins
Myogenesis
Glucose transporter
Skeletal muscle
Biological Transport
Cell Biology
Cell biology
Rats
Slow-Twitch Muscle Fiber
ErbB Receptors
Endocrinology
medicine.anatomical_structure
Glucose
Muscle Fibers, Slow-Twitch
Muscle Fibers, Fast-Twitch
Neuregulin
Tyrosine
Calcium
medicine.symptom
Muscle contraction
Muscle Contraction
Subjects
Details
- ISSN :
- 00219258
- Volume :
- 281
- Issue :
- 31
- Database :
- OpenAIRE
- Journal :
- The Journal of biological chemistry
- Accession number :
- edsair.doi.dedup.....c107e740afc9218e61af3dbbbb18107e