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Record W2380147224

Fibroblast Growth Factor Receptor-2 Involved in FGF-21-mediated Glucose Metabolism

2009· article· en· W2380147224 on OpenAlexaff
Ren Gui

Bibliographic record

Venuenot available
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicFibroblast Growth Factor Research
Canadian institutionsCAE (Canada)
Fundersnot available
KeywordsFibroblast growth factorReceptorChemistryAdipocyteInsulin receptorFGF21Lipid metabolismCell biologyBiochemistryInternal medicineEndocrinologyBiologyAdipose tissueInsulinInsulin resistanceMedicine
DOInot available

Abstract

fetched live from OpenAlex

FGF-21 is a new member of FGF family and reported to regulate glucose metabolism, as well as lipid homeostasis, therefore, FGF-21 is a potential therapeutics for treatment of diabetes and metabolic syndrome. However, little is known about its functional receptor(s) and mechanism of action. The aim of the paper is to investigate the functional receptor(s) for FGF-21 in order to understand the mechanism of action of the molecule. Previous result showed that FGF-21 could stimulate glucose uptake in differentiated 3T3L1 adipocytes, but not in pre-adipocytes, suggesting that differentiated 3T3L1 adipocytes express functional receptor (s) for FGF-21. Therefore, the differentiated 3T3L1 adipocyte is a perfect target for searching receptor (s) of FGF-21. 3T3L1 pre-adipocytes were differentiated into adipocytes. The cell membrane of the life adipocytes were incubated with FGF-21 which was labeled with either Flag-tag or biotin, the FGF-21/receptor complexes were cross-linked once they interacted by cross-link reagent BS3. The FGF-21/receptor complexes were immunoprecipitated by either Flag antibody or streptavidin and analyzed by SDS-PAGE. The results showed that FGF-21 could form putative FGF-21/receptor (s) complexes with surface membrane protein of differentiated 3T3L1 adipocytes, not pre-adipocytes. The molecular mass of the complexes is proximate 300~400 ku. The complexes were formed by the FGF-21 labeled with either Flag-tag or biotin, suggesting the complex formation was not influenced by different labeling. To understand the component of the FGF-21/receptor(s) complexes, Western blot assay was used to examine the interaction of the complexes with known antibodies. FGFR-2 was detected within the FGF-21/receptor complexes by specific antibody for FGFR-2. To confirm the specific relationship between FGF-21 and FGFR-2, FGF-21-induced FGFR-2 tyrosine-phosphorylation was studied in 3T3L1 adipocytes. The results showed that although FGFR-2 was expressed in both pre-adipocytes and adipocytes FGF-21 could only enable adipocyte-expressed FGFR-2 tyrosine phosphorylation, which was consistent with glucose-uptake by FGF-21 in this two cell types. FGF-21 not only phosphorylated in situ adipocyte-expressed FGFR-2, but also ectopically expressed FGFR-2 in mouse pre-B cell line BaF3 cells. Sequencing analysis of FGFR-2 cDNA fromadipocytes revealed that FGFR-2Ⅲc was the only subtype of FGFR-2 expressed in adipocytes, suggesting that FGFR-2Ⅲc is at least one of the functional receptors for FGF-21 and involved in glucose metabolism in the cells. In order to understand the reason why the same FGFR-2 only functions in adipocyte and not in pre-adipocytes, differential expression of FGFR-2 before and after 3T3L1 cell differentiation was systematically analyzed, the result showed that adipocytes expressed high level precursors of FGFR-2, which were not observed in pre-adipocytes, suggesting FGFR-2 turn-over rate could be a key factor to determine the function the molecule. Alternatively, adipocyte-specific molecules could be another key factor participating the signal transduction of FGF-21.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesMeta-epidemiology (narrow)
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.085
Threshold uncertainty score1.000

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.012
GPT teacher head0.255
Teacher spread0.243 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2009
Admission routes1
Has abstractyes

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