Gene expression profile of rat adipose tissue at the onset of high-fat-diet obesity
Abstract
Morbid obesity is the result of massive expansion of white adipose tissue (WAT) and requires recruitment of adipocyte precursor cells and their supporting infrastructure. To characterize the change in the expression profile of the preexisting WAT at the start of obesity, when adipocyte hypertrophy is present but hyperplasia is still minimal, we employed a cDNA subtraction screen for genes differentially expressed in epididymal fat pads harvested 1 wk after the start of a 60% fat diet. Ninety-six genes were upregulated by at least 50% above the WAT of control rats receiving a 4% fat diet. Of these genes, 30 had not previously been identified. Sixteen of the 96 genes, including leptin, adipocyte complement-related protein 30 kDa, and resistin, were predicted to encode a signal peptide. Ten of the 16 had been previously identified in other tissues and implicated in cell growth, proliferation, differentiation, cell cycle control, and angiogenesis. One was a novel gene. Twenty-nine novel fragments were identified. Thus, at the onset of high-fat-diet-induced obesity in rats, adipose tissue increases its expression of factors previously implicated in the expansion of nonadipocyte tissues and of several uncharacterized novel factors. The only one of these thus far characterized functionally was found to promote lipogenesis.
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In rodents, one week of high-fat feeding is enough to enlarge adipocytes, which store four times as much triglyceride per cell as at baseline.
“It takes as little as one week of high-fat feeding (HFF) in rodents for adipocytes to become enlarged, storing four-fold the amount of triglyceride per cell compared with baseline (1).”
From The ominous triad of adipose tissue dysfunction: inflammation, fibrosis, and impaired angiogenesis. (2017) · cites this paper as [1]
Acute high-fat feeding induces antiinflammatory immune cell actions, cell repair signaling, and angiogenesis.
“that acute HFF induces antiinflammatory immune cell actions, cell repair signaling, and angiogenesis (1,17,18).”
From The ominous triad of adipose tissue dysfunction: inflammation, fibrosis, and impaired angiogenesis. (2017) · cites this paper as [1]
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References 41 · Cited by 153
- Authors
- Li, J., Yu, X., Pan, W., & Unger, R. H.
- Affiliations
- The University of Texas Southwestern Medical Center (US)
- Veterans Health Administration (US)
- Venue
- American Journal of Physiology-Endocrinology and Metabolism
- Publisher
- American Physiological Society
- Published
- 2002-06-01
- Volume
- 282
- Issue
- 6
- Pages
- E1334-E1341
- ISSN
- 0193-1849 (ISSN-L)
- 1522-1555
- OpenAlex
- W2115971158
- Cited by
- 153
- References
- 41
- Citations by year
- 2025: 3 · 2024: 4 · 2023: 2 · 2022: 5 · 2021: 3 · 2020: 5 · 2019: 5 · 2018: 4 · 2017: 3 · 2016: 2 · 2015: 5 · 2014: 8 · 2013: 5 · 2012: 8
- FWCI
- 9.38
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- American Journal of Physiology-Endocrinology and Metabolism (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Diabetes and Digestive and Kidney Diseases (DK0270037, 5POI DK58398)
- 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 › Biochemistry › Lipid metabolism and biosynthesis
- Keywords
- high-fat diet-induced obesity, white adipose tissue, gene expression profiles, epididymal adipose tissue, adipocyte hypertrophy, adipocyte hyperplasia, adipose tissue expansion, leptin, adiponectin, resistin, angiogenesis, lipogenesis
- MeSH terms
- Adipose Tissue, Animals, Blood Proteins, Cytoskeletal Proteins, Dietary Fats, Hormones, Ectopic, Hyperplasia, Hypertrophy, Lipids, Male, Mitochondria, Nutritional Physiological Phenomena, Obesity, Oxygen Consumption, Proteins, RNA, Messenger, Transcription Factors, Tumor Necrosis Factor-alpha, Signal Transduction, Rats, Sprague-Dawley, Adipocytes, Reverse Transcriptase Polymerase Chain Reaction, Leptin, Gene Expression Profiling, Nerve Growth Factor, Intercellular Signaling Peptides and Proteins, Rats, Adiponectin, Resistin
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