» Articles » PMID: 24273516

Skeletal Muscle Heat Shock Protein 70: Diverse Functions and Therapeutic Potential for Wasting Disorders

Overview
Journal Front Physiol
Date 2013 Nov 26
PMID 24273516
Citations 41
Authors
Affiliations
Soon will be listed here.
Abstract

The stress-inducible 70-kDa heat shock protein (HSP70) is a highly conserved protein with diverse intracellular and extracellular functions. In skeletal muscle, HSP70 is rapidly induced in response to both non-damaging and damaging stress stimuli including exercise and acute muscle injuries. This upregulation of HSP70 contributes to the maintenance of muscle fiber integrity and facilitates muscle regeneration and recovery. Conversely, HSP70 expression is decreased during muscle inactivity and aging, and evidence supports the loss of HSP70 as a key mechanism which may drive muscle atrophy, contractile dysfunction and reduced regenerative capacity associated with these conditions. To date, the therapeutic benefit of HSP70 upregulation in skeletal muscle has been established in rodent models of muscle injury, muscle atrophy, modified muscle use, aging, and muscular dystrophy, which highlights HSP70 as a key therapeutic target for the treatment of various conditions which negatively affect skeletal muscle mass and function. This article will review these important findings and provide perspective on the unanswered questions related to HSP70 and skeletal muscle plasticity which require further investigation.

Citing Articles

Effective adaptation of flight muscles to tebuconazole-induced oxidative stress in honey bees.

Mackei M, Huber F, Sebok C, Voroshazi J, Traj P, Marton R Heliyon. 2025; 11(1):e41291.

PMID: 39811324 PMC: 11730214. DOI: 10.1016/j.heliyon.2024.e41291.


Effects of thermal interventions on skeletal muscle adaptations and regeneration: perspectives on epigenetics: a narrative review.

Normand-Gravier T, Solsona R, Dablainville V, Racinais S, Borrani F, Bernardi H Eur J Appl Physiol. 2024; 125(2):277-301.

PMID: 39607529 PMC: 11829912. DOI: 10.1007/s00421-024-05642-9.


Amino acids regulating skeletal muscle metabolism: mechanisms of action, physical training dosage recommendations and adverse effects.

Li G, Li Z, Liu J Nutr Metab (Lond). 2024; 21(1):41.

PMID: 38956658 PMC: 11220999. DOI: 10.1186/s12986-024-00820-0.


Proteomic reference map for sarcopenia research: mass spectrometric identification of key muscle proteins of organelles, cellular signaling, bioenergetic metabolism and molecular chaperoning.

Dowling P, Gargan S, Zweyer M, Henry M, Meleady P, Swandulla D Eur J Transl Myol. 2024; 34(2).

PMID: 38787292 PMC: 11264233. DOI: 10.4081/ejtm.2024.12565.


Non-coding RNA regulation of Magang geese skeletal muscle maturation via the MAPK signaling pathway.

Hong L, Xu D, Li W, Wang Y, Cao N, Fu X Front Physiol. 2024; 14:1331974.

PMID: 38314139 PMC: 10834734. DOI: 10.3389/fphys.2023.1331974.


References
1.
Hernando R, Manso R . Muscle fibre stress in response to exercise: synthesis, accumulation and isoform transitions of 70-kDa heat-shock proteins. Eur J Biochem. 1997; 243(1-2):460-7. DOI: 10.1111/j.1432-1033.1997.0460a.x. View

2.
Han R, Frett E, Levy J, Rader E, Lueck J, Bansal D . Genetic ablation of complement C3 attenuates muscle pathology in dysferlin-deficient mice. J Clin Invest. 2010; 120(12):4366-74. PMC: 2993587. DOI: 10.1172/JCI42390. View

3.
Chung J, Nguyen A, Henstridge D, Holmes A, Chan M, Mesa J . HSP72 protects against obesity-induced insulin resistance. Proc Natl Acad Sci U S A. 2008; 105(5):1739-44. PMC: 2234214. DOI: 10.1073/pnas.0705799105. View

4.
Morton J, Kayani A, McArdle A, Drust B . The exercise-induced stress response of skeletal muscle, with specific emphasis on humans. Sports Med. 2009; 39(8):643-62. DOI: 10.2165/00007256-200939080-00003. View

5.
Kovalchin J, Wang R, Wagh M, Azoulay J, Sanders M, Chandawarkar R . In vivo delivery of heat shock protein 70 accelerates wound healing by up-regulating macrophage-mediated phagocytosis. Wound Repair Regen. 2006; 14(2):129-37. DOI: 10.1111/j.1743-6109.2006.00102.x. View