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Bruce M. Spiegelman

Researcher at Harvard University

Publications -  443
Citations -  172265

Bruce M. Spiegelman is an academic researcher from Harvard University. The author has contributed to research in topics: Adipose tissue & Transcription factor. The author has an hindex of 179, co-authored 434 publications receiving 158009 citations. Previous affiliations of Bruce M. Spiegelman include University of California, San Francisco & Vassar College.

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Transcriptional coactivator PGC-1α controls the energy state and contractile function of cardiac muscle

TL;DR: Using genetic knockout mice, it is shown that, while PGC-1alpha KO mice appear to retain normal mitochondrial volume in both muscle beds, expression of genes of oxidative phosphorylation is markedly blunted, indicating that P GC-1 alpha is vital for the heart to meet increased demands for ATP and work in response to physiological stimuli.
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PPARγ agonists Induce a White-to-Brown Fat Conversion through Stabilization of PRDM16 Protein

TL;DR: It is shown that PPARγ ligands require full agonism to induce a brown fat gene program preferentially in subcutaneous white adipose cells, and that compounds that stabilize PRDM16 protein may represent a plausible therapeutic pathway for the treatment of obesity and diabetes.
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Regulation of PPAR gamma gene expression by nutrition and obesity in rodents.

TL;DR: PPAR gamma 2 mRNA expression is most abundant in adipocytes in normal mice, but lower level expression is seen in skeletal muscle, which demonstrates in vivo modulation of PPAR gamma mRNA levels over a fourfold range and provide an additional level of regulation for the control of adipocyte development and function.
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Transdifferentiation of myoblasts by the adipogenic transcription factors PPAR gamma and C/EBP alpha

TL;DR: The results demonstrate that a developmental switch between these two related but highly specialized cell types can be controlled by the expression of key adipogenic transcription factors.
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Initiation of myoblast to brown fat switch by a PRDM16-C/EBP-beta transcriptional complex.

TL;DR: It is shown that PRDM16 forms a transcriptional complex with the active form of C/EBP-β (also known as LAP), acting as a critical molecular unit that controls the cell fate switch from myoblastic precursors to brown fat cells.