Forming functional fat: a growing understanding of adipocyte differentiation
Open accessAbstract
Adipose tissue, which is primarily composed of adipocytes, is crucial for maintaining energy and metabolic homeostasis. Adipogenesis is thought to occur in two stages: commitment of mesenchymal stem cells to a preadipocyte fate and terminal differentiation. Cell shape and extracellular matrix remodelling have recently been found to regulate preadipocyte commitment and competency by modulating WNT and RHO-family GTPase signalling cascades. Adipogenic stimuli induce terminal differentiation in committed preadipocytes through the epigenomic activation of peroxisome proliferator-activated receptor-γ (PPARγ). The coordination of PPARγ with CCAAT/enhancer-binding protein (C/EBP) transcription factors maintains adipocyte gene expression. Improving our understanding of these mechanisms may allow us to identify therapeutic targets against metabolic diseases that are rapidly becoming epidemic globally.
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STAT3 facilitates adipogenesis from preadipocytes through epigenetic activation of PPARγ and transcriptional upregulation of C/EBPβ.
“STAT3 facilitates adipogenesis from preadipocytes”
From Targeting Janus Kinases and Signal Transducer and Activator of Transcription 3 To Treat Inflammation, Fibrosis, and Cancer: Rationale, Progress, and Caution (2020) · cites this paper as Cristancho and Lazar, 2011
The ‘C/EBP activation by adipogenic stimuli’ section says that a JAK2–STAT3 cascade directly promotes C/EBPβ expression in committed preadipocytes, supporting the printed sentence. The ‘Epigenomics provides insights into early PPARγ activation’ section discusses epigenetic regulation of PPARγ but does not attribute that regulation to STAT3, so the fuller quoted mechanism is not fully supported. No page numbers are available in our copy. (LLM, conf=0.86)
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Matrix elasticity directs stem cell lineage specification
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Functional Brown Adipose Tissue in Healthy Adults
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Dynamics of fat cell turnover in humans
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“Interestingly, lineage-tracing studies ( Box 1 ) have revealed that BAT is more closely related to skeletal muscle than WAT, as both muscle and BAT have progenitors that express the early muscle marker myogenic factor 5 (MYF5) but WAT does no”
BackgroundFat and Beyond: The Diverse Biology of PPARγ
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- Authors
- Cristancho, A. G., & Lazar, M. A.
- Affiliations
- University of Pennsylvania (US)
- Corresponding author
- Lazar, Mitchell A.
- Venue
- Nature Reviews Molecular Cell Biology
- Published
- 2011-09-28
- Volume
- 12
- Issue
- 11
- Pages
- 722-734
- ISSN
- 1471-0072 (ISSN-L)
- 1471-0080
- PMC
- PMC7171550
- OpenAlex
- W2016701686
- Cited by
- 1,382
- References
- 9
- Citations by year
- 2026: 50 · 2025: 67 · 2024: 101 · 2023: 87 · 2022: 107 · 2021: 99 · 2020: 93 · 2019: 98 · 2018: 102 · 2017: 110 · 2016: 109 · 2015: 97 · 2014: 105 · 2013: 95 · 2012: 61
- FWCI
- 7.61
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature Reviews Molecular Cell Biology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Howard Hughes Medical Institute
- National Institutes of Health (5r01dk049780-29)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK49780, R01-DK049780)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Peroxisome Proliferator-Activated Receptors
- Health Sciences › Medicine › Physiology › Adipose Tissue and Metabolism
- Health Sciences › Medicine › Epidemiology › Adipokines, Inflammation, and Metabolic Diseases
- Keywords
- adipogenesis, mesenchymal stem cells, terminal differentiation, extracellular matrix remodeling, cell shape, Wnt signaling, Rho GTPase signaling, PPARγ, C/EBP transcription factors, epigenetic regulation, metabolic disorders, adipose tissue
- MeSH terms
- Animals, Cell Differentiation, Extracellular Matrix, Humans, Models, Biological, Signal Transduction, Transforming Growth Factor beta, Adipocytes, Cell Lineage, rho GTP-Binding Proteins, CCAAT-Enhancer-Binding Proteins, Epigenesis, Genetic, PPAR gamma, Cell Shape, Adipogenesis, Mesenchymal Stem Cells, Wnt Signaling Pathway
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