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Identification and Clinical Associations of 3 Forms of Circulating T-cadherin in Human Serum

Authors :
Yuya Fujishima
Masahito Iioka
Tadashi Nakamura
Shiro Fukuda
Kazuya Miyashita
Jun Morinaga
Hitoshi Nishizawa
Yuichi Oike
Iichiro Shimomura
Shunbun Kita
Jun Murai
Norikazu Maeda
Source :
The Journal of Clinical Endocrinology and Metabolism
Publication Year :
2021
Publisher :
Oxford University Press, 2021.

Abstract

Context T-cadherin (T-cad) is a glycosylphosphatidylinositol (GPI)-anchored cadherin that mediates adiponectin to induce exosome biogenesis and secretion, protect cardiovascular tissues, promote muscle regeneration, and stimulate therapeutic heart protection by transplanted mesenchymal stem cells. CDH13, the gene locus of T-cad, affects plasma adiponectin levels most strongly, in addition to affecting cardiovascular disease risk and glucose homeostasis. Recently, it has been suggested that T-cad exists in human serum, although the details are still unclear. Objective To validate the existence of T-cad forms in human serum and investigate the association with clinical parameters of type 2 diabetes patients. Methods Using newly developed monoclonal antibodies against T-cad, pooled human serum was analyzed, and novel T-cad enzyme-linked immunosorbent assays (ELISAs) were developed. The serum T-cad concentrations of 183 Japanese type 2 diabetes patients were measured in a cross-sectional observational study. The main outcome measure was the existence of soluble T-cad in human serum. Results There were 3 forms of soluble T-cad: a 130-kDa form with a prodomain, a 100-kDa mature form, and a 30-kDa prodomain in human serum. Using newly developed ELISAs to measure them simultaneously, we found that the 130-kDa form of T-cad positively correlated with plasma adiponectin (r = 0.28, P Conclusion We identified 3 novel forms of soluble T-cad. Their importance as disease markers and/or biomarkers of adiponectin function and the possible bioactivity of the respective molecules require further investigation.

Details

Language :
English
ISSN :
19457197 and 0021972X
Volume :
106
Issue :
5
Database :
OpenAIRE
Journal :
The Journal of Clinical Endocrinology and Metabolism
Accession number :
edsair.doi.dedup.....69fe87d6d8a363d9c119bea77ee539e9