Key result
Caveolin-1 null mice showed markedly decreased body temperatures and failed to increase serum nonesterified fatty acids in response to fasting or fasting/cold treatment compared to wild-type mice.
Why the study?
Does caveolin-1 deficiency affect nonshivering thermogenesis and lipid mobilization in brown adipose tissue in mice?
Does caveolin-1 deficiency affect nonshivering thermogenesis and lipid mobilization in brown adipose tissue in mice?
Caveolin-1 plays a critical functional and structural role in modulating thermogenesis via lipid mobilization in brown adipose tissue.
Answers are grounded in this paper and cite their sources.
Caveolin-1 may modulate BAT thermogenesis in mice; leaves open human relevance and clinical translation.
Recently, we have shown that loss of caveolin-1 leads to marked alterations in insulin signaling and lipolysis in white adipose tissue. However, little is known about the role of caveolin-1 in brown adipose tissue (BAT), a tissue responsible for nonshivering thermogenesis. Here, we show that caveolin-1 null mice have a mildly, yet significantly, decreased resting core body temperature. To investigate this in detail, we next subjected the mice to fasting (for 24 h) or cold treatment (4 degrees C for 24 h), individually or in combination. Interestingly, caveolin-1 null mice showed markedly decreased body temperatures in response to fasting or fasting/cold treatment; however, cold treatment alone had no effect. In addition, under these conditions caveolin-1 null mice failed to show the normal increase in serum nonesterified fatty acids induced by fasting or fasting/cold treatment, suggesting that these mice are unable to liberate triglyceride stores for heat production. In accordance with these results, the triglyceride content of BAT was reduced nearly 10-fold in wild-type mice after fasting/cold treatment, but it was reduced only 3-fold in caveolin-1 null mice. Finally, electron microscopy of adipose tissue revealed dramatic perturbations in the mitochondria of caveolin-1 null interscapular brown adipocytes. Taken together, our data provide the first molecular genetic evidence that caveolin-1 plays a critical functional and structural role in the modulation of thermogenesis via an effect on lipid mobilization.
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Cohen et al. (2005) studied this question. Caveolin-1 null mutation vs. Wild-type mice was evaluated on Body temperature and triglyceride content in response to fasting or cold treatment. Caveolin-1 null mice showed markedly decreased body temperatures and failed to increase serum nonesterified fatty acids in response to fasting or fasting/cold treatment compared to wild-type mice.
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