Cited by 61Signaling Pathways in DiseasePeroxisome Proliferator-Activated ReceptorsAdipokines, Inflammation, and Metabolic Diseases

The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.

Identification and characterization of an immunophilin expressed during the clonal expansion phase of adipocyte differentiation.

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Yeh, W C, Li, T K, Bierer, B E, McKnight, S L·1995·Proceedings of the National Academy of Sciences

Abstract

Mouse 3T3-L1 cells differentiate into fat-laden adipocytes in response to a cocktail of adipogenic hormones. This conversion process occurs in two discrete steps. During an early clonal expansion phase, confluent 3T3-L1 cells proliferate and express the products of the beta and delta members of the CCAAT/enhancer binding protein (C/EBP) family of transcription factors. The cells subsequently arrest mitotic growth, induce the expression of the alpha form of C/EBP, and acquire the morphology of fully differentiated adipocytes. Many of the genes induced during the terminal phase of adipocyte conversion are directly activated by C/EBP alpha, and gratuitous expression of this transcription factor is capable of catalyzing adipose conversion in a number of different cultured cell lines. The genetic program undertaken during the clonal expansion phase of 3T3-L1 differentiation, controlled in part by C/EBP beta and C/EBP delta, is less clearly understood. To study the molecular events occurring during clonal expansion, we have identified mRNAs that selectively accumulate during this phase of adipocyte conversion. One such mRNA encodes an immunophilin hereby designated FKBP51. In this report we provide the initial molecular characterization of FKBP51.

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Crossref · 10.1073/pnas.92.24.11081

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Metadata

Authors
Yeh, W. C., Li, T. K., Bierer, B. E., & McKnight, S. L.
Affiliations
  • Johns Hopkins University (US)
  • Amgen (United States) (US)
Venue
Proceedings of the National Academy of Sciences
Published
1995-11-21
Volume
92
Issue
24
Pages
11081-11085
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W1973391327
Cited by
61
References
5
Citations by year
2023: 3 · 2022: 2 · 2021: 1 · 2019: 1 · 2017: 2 · 2016: 3 · 2015: 3 · 2014: 4 · 2013: 4 · 2012: 2
FWCI
0.99
Type
journal article
Language
en
Open access
Locations
  • Proceedings of the National Academy of Sciences (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health (5r01ai032514-05)
  • National Institute of Allergy and Infectious Diseases (AI32514)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Signaling Pathways in Disease
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Peroxisome Proliferator-Activated Receptors
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adipokines, Inflammation, and Metabolic Diseases
Keywords
FKBP51, immunophilins, adipogenesis, 3T3-L1 cells, clonal expansion, C/EBPβ, C/EBPδ, C/EBPα, transcription factors, mRNA accumulation, gene expression regulation
MeSH terms
Amino Acid Isomerases, Amino Acid Sequence, Animals, Carrier Proteins, Cell Differentiation, Clone Cells, DNA-Binding Proteins, Heat-Shock Proteins, Molecular Sequence Data, Polyenes, RNA, Messenger, Tissue Distribution, Gene Expression, Sequence Alignment, Tacrolimus, Sequence Homology, Amino Acid, Adipocytes, Peptidylprolyl Isomerase, Sirolimus, Tacrolimus Binding Proteins, Mice

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