Sarcolipin is a newly identified regulator of muscle-based thermogenesis in mammals
Author(s) -
Naresh C. Bal,
Santosh K. Maurya,
Danesh H. Sopariwala,
Sanjaya Kumar Sahoo,
Subash Gupta,
Sana Shaikh,
Meghna Pant,
Leslie A. Rowland,
Éric Bombardier,
Sanjeewa A. Goonasekera,
A. Russell Tupling,
Jeffery D. Molkentin,
Muthu Periasamy
Publication year - 2012
Publication title -
nature medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 19.536
H-Index - 547
eISSN - 1546-170X
pISSN - 1078-8956
DOI - 10.1038/nm.2897
Subject(s) - serca , thermogenesis , skeletal muscle , ryanodine receptor , endocrinology , biology , medicine , endoplasmic reticulum , thermogenin , microbiology and biotechnology , atpase , brown adipose tissue , adipose tissue , biochemistry , enzyme
The role of skeletal muscle in nonshivering thermogenesis (NST) is not well understood. Here we show that sarcolipin (Sln), a newly identified regulator of the sarco/endoplasmic reticulum Ca(2+)-ATPase (Serca) pump, is necessary for muscle-based thermogenesis. When challenged to acute cold (4 °C), Sln(-/-) mice were not able to maintain their core body temperature (37 °C) and developed hypothermia. Surgical ablation of brown adipose tissue and functional knockdown of Ucp1 allowed us to highlight the role of muscle in NST. Overexpression of Sln in the Sln-null background fully restored muscle-based thermogenesis, suggesting that Sln is the basis for Serca-mediated heat production. We show that ryanodine receptor 1 (Ryr1)-mediated Ca(2+) leak is an important mechanism for Serca-activated heat generation. Here we present data to suggest that Sln can continue to interact with Serca in the presence of Ca(2+), which can promote uncoupling of the Serca pump and cause futile cycling. We further show that loss of Sln predisposes mice to diet-induced obesity, which suggests that Sln-mediated NST is recruited during metabolic overload. These data collectively suggest that SLN is an important mediator of muscle thermogenesis and whole-body energy metabolism.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom