The molecular identity of the TLQP-21 peptide receptor

被引:0
|
作者
Bhavani S. Sahu
Megin E. Nguyen
Pedro Rodriguez
Jean Pierre Pallais
Vinayak Ghosh
Maria Razzoli
Yuk Y. Sham
Stephen R. Salton
Alessandro Bartolomucci
机构
[1] National Brain Research Centre,Department of Integrative Biology and Physiology
[2] University of Minnesota,Bioinformatics and Computational Biology Program
[3] University of Minnesota,Departments of Neuroscience and Geriatrics and Palliative Medicine
[4] Friedman Brain Institute,undefined
[5] Icahn School of Medicine at Mount Sinai,undefined
来源
关键词
G-protein-coupled receptor; VGF; TLQP-21; C3aR1; C3a; gC1QR; HSPA8; Complement; Microglia; Adipocytes;
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学科分类号
摘要
The TLQP-21 neuropeptide has been implicated in functions as diverse as lipolysis, neurodegeneration and metabolism, thus suggesting an important role in several human diseases. Three binding targets have been proposed for TLQP-21: C3aR1, gC1qR and HSPA8. The aim of this review is to critically evaluate the molecular identity of the TLQP-21 receptor and the proposed multi-receptor mechanism of action. Several studies confirm a critical role for C3aR1 in TLQP-21 biological activity and a largely conserved mode of binding, receptor activation and signaling with C3a, its first-identified endogenous ligand. Conversely, data supporting a role of gC1qR and HSPA8 in TLQP-21 activity remain limited, with no signal transduction pathways being described. Overall, C3aR1 is the only receptor for which a necessary and sufficient role in TLQP-21 activity has been confirmed thus far. This conclusion calls into question the validity of a multi-receptor mechanism of action for TLQP-21 and should inform future studies.
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页码:7133 / 7144
页数:11
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