Regulatory circuits controlling white versus brown adipocyte differentiation.

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Regulatory circuits controlling white versus brown adipocyte differentiation. / Hansen, Jacob B; Kristiansen, Karsten.

In: Biochemical Journal, Vol. 398, No. 2, 2006, p. 153-68.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Hansen, JB & Kristiansen, K 2006, 'Regulatory circuits controlling white versus brown adipocyte differentiation.', Biochemical Journal, vol. 398, no. 2, pp. 153-68. https://doi.org/10.1042/BJ20060402

APA

Hansen, J. B., & Kristiansen, K. (2006). Regulatory circuits controlling white versus brown adipocyte differentiation. Biochemical Journal, 398(2), 153-68. https://doi.org/10.1042/BJ20060402

Vancouver

Hansen JB, Kristiansen K. Regulatory circuits controlling white versus brown adipocyte differentiation. Biochemical Journal. 2006;398(2):153-68. https://doi.org/10.1042/BJ20060402

Author

Hansen, Jacob B ; Kristiansen, Karsten. / Regulatory circuits controlling white versus brown adipocyte differentiation. In: Biochemical Journal. 2006 ; Vol. 398, No. 2. pp. 153-68.

Bibtex

@article{21078450ab5a11ddb5e9000ea68e967b,
title = "Regulatory circuits controlling white versus brown adipocyte differentiation.",
abstract = "Adipose tissue is a major endocrine organ that exerts a profound influence on whole-body homoeostasis. Two types of adipose tissue exist in mammals: WAT (white adipose tissue) and BAT (brown adipose tissue). WAT stores energy and is the largest energy reserve in mammals, whereas BAT, expressing UCP1 (uncoupling protein 1), can dissipate energy through adaptive thermogenesis. In rodents, ample evidence supports BAT as an organ counteracting obesity, whereas less is known about the presence and significance of BAT in humans. Despite the different functions of white and brown adipocytes, knowledge of factors differentially influencing the formation of white and brown fat cells is sparse. Here we summarize recent progress in the molecular understanding of white versus brown adipocyte differentiation, including novel insights into transcriptional and signal transduction pathways. Since expression of UCP1 is the hallmark of BAT and a key factor determining energy expenditure, we also review conditions associated with enhanced energy expenditure and UCP1 expression in WAT that may provide information on processes involved in brown adipocyte differentiation.",
author = "Hansen, {Jacob B} and Karsten Kristiansen",
note = "Keywords: Adipose Tissue; Adipose Tissue, Brown; Animals; Carrier Proteins; Cell Differentiation; Gene Expression Regulation; Humans; Ion Channels; Membrane Proteins; Mitochondrial Proteins; Signal Transduction",
year = "2006",
doi = "10.1042/BJ20060402",
language = "English",
volume = "398",
pages = "153--68",
journal = "Biochemical Journal",
issn = "0264-6021",
publisher = "Portland Press Ltd.",
number = "2",

}

RIS

TY - JOUR

T1 - Regulatory circuits controlling white versus brown adipocyte differentiation.

AU - Hansen, Jacob B

AU - Kristiansen, Karsten

N1 - Keywords: Adipose Tissue; Adipose Tissue, Brown; Animals; Carrier Proteins; Cell Differentiation; Gene Expression Regulation; Humans; Ion Channels; Membrane Proteins; Mitochondrial Proteins; Signal Transduction

PY - 2006

Y1 - 2006

N2 - Adipose tissue is a major endocrine organ that exerts a profound influence on whole-body homoeostasis. Two types of adipose tissue exist in mammals: WAT (white adipose tissue) and BAT (brown adipose tissue). WAT stores energy and is the largest energy reserve in mammals, whereas BAT, expressing UCP1 (uncoupling protein 1), can dissipate energy through adaptive thermogenesis. In rodents, ample evidence supports BAT as an organ counteracting obesity, whereas less is known about the presence and significance of BAT in humans. Despite the different functions of white and brown adipocytes, knowledge of factors differentially influencing the formation of white and brown fat cells is sparse. Here we summarize recent progress in the molecular understanding of white versus brown adipocyte differentiation, including novel insights into transcriptional and signal transduction pathways. Since expression of UCP1 is the hallmark of BAT and a key factor determining energy expenditure, we also review conditions associated with enhanced energy expenditure and UCP1 expression in WAT that may provide information on processes involved in brown adipocyte differentiation.

AB - Adipose tissue is a major endocrine organ that exerts a profound influence on whole-body homoeostasis. Two types of adipose tissue exist in mammals: WAT (white adipose tissue) and BAT (brown adipose tissue). WAT stores energy and is the largest energy reserve in mammals, whereas BAT, expressing UCP1 (uncoupling protein 1), can dissipate energy through adaptive thermogenesis. In rodents, ample evidence supports BAT as an organ counteracting obesity, whereas less is known about the presence and significance of BAT in humans. Despite the different functions of white and brown adipocytes, knowledge of factors differentially influencing the formation of white and brown fat cells is sparse. Here we summarize recent progress in the molecular understanding of white versus brown adipocyte differentiation, including novel insights into transcriptional and signal transduction pathways. Since expression of UCP1 is the hallmark of BAT and a key factor determining energy expenditure, we also review conditions associated with enhanced energy expenditure and UCP1 expression in WAT that may provide information on processes involved in brown adipocyte differentiation.

U2 - 10.1042/BJ20060402

DO - 10.1042/BJ20060402

M3 - Journal article

C2 - 16898874

VL - 398

SP - 153

EP - 168

JO - Biochemical Journal

JF - Biochemical Journal

SN - 0264-6021

IS - 2

ER -

ID: 8419316