Evidence map›Paper›PMID 40695744›Full record

ArticleDiabetes & metabolism journal2025

Construction of a Novel Secreted Protein Database and Identification of a New Adipokine CRELD2.

Shu-Na Wang, Zhi-Yong Li, Qi-Sheng Ling, Peng-Fei Jing, Wen-Yu Liu, Yi-Jie Zhang, Xiu-Ping Zhang, Xi-Yuan Wang, Fu-Qiang Chang, Zhu-Wei Miao and 3 more

Abstract read
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Article in Diabetes & metabolism journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Shu-Na Wang *Department of Pharmacology, Second Military Medical University (Naval Medical University), Shanghai, China.
Zhi-Yong Li *Department of Pharmacology, Second Military Medical University (Naval Medical University), Shanghai, China.
Qi-Sheng Ling *Department of Pharmacology, Second Military Medical University (Naval Medical University), Shanghai, China.
Peng-Fei Jing *Department of Pharmacology, Second Military Medical University (Naval Medical University), Shanghai, China.
Wen-Yu LiuDepartment of Pancreatic and Hepatobiliary Surgery, Changhai Hospital, Second Military Medical University (Naval Medical University), Shanghai, China.
Yi-Jie ZhangDepartment of Pancreatic and Hepatobiliary Surgery, Changhai Hospital, Second Military Medical University (Naval Medical University), Shanghai, China.
Xiu-Ping ZhangDepartment of Pharmacology, Second Military Medical University (Naval Medical University), Shanghai, China.
Xi-Yuan WangDepartment of Pharmacology, Second Military Medical University (Naval Medical University), Shanghai, China.
Fu-Qiang ChangDepartment of Pharmacology, Second Military Medical University (Naval Medical University), Shanghai, China.
Zhu-Wei MiaoDepartment of Pharmacology, Second Military Medical University (Naval Medical University), Shanghai, China.
Jing-Xin ZhaoDepartment of Pharmacology, Second Military Medical University (Naval Medical University), Shanghai, China.
Jin ChenDepartment of Pharmacology, Second Military Medical University (Naval Medical University), Shanghai, China.
Chao-Yu MiaoDepartment of Pharmacology, Second Military Medical University (Naval Medical University), Shanghai, China.

Funding

National Natural Science Foundation of China 81130061National Natural Science Foundation of China 82003754National Natural Science Foundation of China 82030110National Natural Science Foundation of China 82330117Shanghai Science and Technology Commission Project 20YF1458400Shanghai Science and Technology Commission Project 23ZR1477400
6 · The paper itself

Abstract

backgruoundSecreted proteins may become therapeutic targets, drugs and biomarkers for aging and disease. This study aimed to establish a novel secreted protein database for adipose tissue under access to food ad libitum (AL) and caloric restriction (CR), and verify a novel adipokine.

methodsTwelve rat chips were used for whole-genome expression in various adipose tissues from AL and CR rats, followed by bioinformatics analysis and experiments in mice, rats, and humans as well as in obesity and diabetes models.

resultsAdipose tissue expression profiles in rat different locations exhibited unique features, and enrichment analysis of differentially expressed genes between CR and AL groups showed CR effects on different adipose tissues. The 1,472 putative secreted proteins were identified, in which 200 genes were highly expressed, constructing a potential adipokines library. Cysteine rich with EGF like domains 2 (CRELD2, also named MESFATIN), whose gene was mesenteric adipose tissue specifically expressed and upregulated by CR in rat chips, was selected and verified as novel adipokine with proving its expression and secretion in in vivo mouse, rat and human and in vitro adipose tissue and adipocyte. CRELD2 secretion increased during adipocyte differentiation, and CRELD2 recombinant protein promoted adipogenesis. Although CRELD2 serum concentration showed no difference between wild-type mice and genetic ob/ob obesity mice or high fat diet induced obesity mice, CRELD2 expression decreased in white adipose tissues of ob/ob mice.

conclusionCRELD2 is a new adipokine involved in adipocyte differentiation and adipogenesis. A novel secreted protein database created from multiple adipose depots with CR intervention is helpful for future discovery and research of more secreted proteins.

Indexed as

AdipokinesAdipose TissueCytokinesDatabases, Protein3T3-L1 CellsAdipocytesAdipogenesisAnimalsCaloric RestrictionHumansMaleMiceMice, Inbred C57BLObesityRatsRats, Sprague-DawleyAdipokinesCytokinesAdipokinesCaloric restrictionCRELD2 protein, humanCRELD2 protein, mouseEndocrine systemObesity

Identifiers

PMID40695744
PMCPMC12436037

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.