Coordinated Regulation of Nutrient and Inflammatory Responses by STAMP2 Is Essential for Metabolic Homeostasis
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Metabolic and inflammatory pathways crosstalk at many levels, and, while required for homeostasis, interaction between these pathways can also lead to metabolic dysregulation under conditions of chronic stress. Thus, we hypothesized that mechanisms might exist to prevent overt inflammatory responses during physiological fluctuations in nutrients or under nutrient-rich conditions, and we identified the six-transmembrane protein STAMP2 as a critical modulator of this integrated response system of inflammation and metabolism in adipocytes. Lack of STAMP2 in adipocytes results in aberrant inflammatory responses to both nutrients and acute inflammatory stimuli. Similarly, in whole animals, visceral adipose tissue of STAMP2(-/-) mice exhibits overt inflammation, and these mice develop spontaneous metabolic disease on a regular diet, manifesting insulin resistance, glucose intolerance, mild hyperglycemia, dyslipidemia, and fatty liver disease. We conclude that STAMP2 participates in integrating inflammatory and metabolic responses and thus plays a key role in systemic metabolic homeostasis.
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Chronic low-grade inflammation is associated with poor iron status in obese persons.
“past and emerging evidence indicates that chronic low-grade inflammation is associated with poor Fe status in obese persons (716 -721) .”
From Dietary factors and low-grade inflammation in relation to overweight and obesity (2011) · cites this paper as [718]
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Hepatic STAMP2 alleviates high fat diet-induced hepatic steatosis and insulin resistance
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Lipids to the Top of Hair Biology
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- Authors
- Wellen, K. E., Fucho, R., Gregor, M. F., Furuhashi, M., Morgan, C., Lindstad, T., Vaillancourt, E., Gorgun, C. Z., Saatcioglu, F., & Hotamisligil, G. S.
- Affiliations
- Harvard University (US)
- University of Oslo (NO)
- ORCID
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2007-05
- Volume
- 129
- Issue
- 3
- Pages
- 537-548
- ISSN
- 0092-8674 (ISSN-L)
- PMC
- PMC2408881
- OpenAlex
- W2134888531
- Cited by
- 222
- References
- 40
- Citations by year
- 2026: 3 · 2025: 8 · 2024: 6 · 2023: 7 · 2022: 13 · 2021: 12 · 2020: 9 · 2019: 11 · 2018: 11 · 2017: 14 · 2016: 16 · 2015: 8 · 2014: 13 · 2013: 15 · 2012: 16
- FWCI
- 11.00
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- cc-by
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 2269 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Cell (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Diabetes and Digestive and Kidney Diseases (DK52539, R01DK052539, T90DK070078, P30DK040561)
- Topics
- Health Sciences › Medicine › Epidemiology › Adipokines, Inflammation, and Metabolic Diseases
- Health Sciences › Medicine › Physiology › Adipose Tissue and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Peroxisome Proliferator-Activated Receptors
- Keywords
- STAMP2, adipocytes, metabolic homeostasis, inflammation, nutrient sensing, metabolic inflammation, visceral adipose tissue, insulin resistance, impaired glucose tolerance, hepatic steatosis, dyslipidemia, chronic stress, metabolic disorders
- MeSH terms
- Adipose Tissue, Animals, Cells, Cultured, Female, Food, Glucose, Homeostasis, Inflammation, Insulin, Insulin Resistance, Liver, Male, Membrane Proteins, Mice, Inbred C57BL, Mutation, Adipocytes, Metabolic Syndrome, 3T3-L1 Cells, Lipid Metabolism, Mice, Metabolic Networks and Pathways
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