Literature DB >> 29799787

FAM19A1 is a new ligand for GPR1 that modulates neural stem-cell proliferation and differentiation.

Can Zheng1,2, Dixin Chen1,2, Yan Zhang1,2, Yun Bai3, Shiyang Huang1,2, Danfeng Zheng1,2, Weiwei Liang1,2, Shaoping She1,2, Xinjian Peng1,2, Pingzhang Wang1,2,4, Xiaoning Mo4, Quansheng Song1,2,4, Ping Lv1,2,4, Jing Huang1,2,4, Richard D Ye5, Ying Wang1,2,4.   

Abstract

FAM19A1 is a member of the family with sequence similarity 19 with unknown function. FAM19A1 mRNA expression is restricted to the CNS. Here, we report that FAM19A1 is a classic secretory protein, and expression levels correlate with brain development, increasing from embryonic d 12.5, peaking between postnatal d (P)1 and P7 and decreasing at wk 8. The adult hippocampus is a region of FAM19A1 high expression. Recombinant FAM19A1 suppressed the proliferation and self-renewal of neural stem cells (NSCs) and altered the lineage progression of NSCs with promoted neuron differentiation and suppressed astrocyte differentiation. Although GPCR 1 (GPR1) has been reported to be expressed in the CNS, its functions in the brain remain unclear. We identified GPR1 to be a functional receptor for FAM19A1. FAM19A1 interacted with GPR1 via the N-terminal domain (GPR1-ND), and its NSC modulatory functions required the Rho-associated protein kinase (ROCK) /ERK1/2 and ROCK/signal transducer and activator of transcription 3 signaling pathways. GPR1-ND that selectively bound to FAM19A1 neutralized the effects of FAM19A1 on NSC functions. Taken together, our results show, for the first time to our knowledge, that FAM19A1 is a novel regulatory factor of the proliferation and differentiation of NSCs, and identified a novel mechanism by which GPCR mediates the effects of FAM19A1 on NSC functions that may be important for brain development and neurogenesis. Additional exploration of the functions of FAM19A1 and GPR1 in the CNS may broaden the range of therapeutic options available for major brain disorders.-Zheng, C., Chen, D., Zhang, Y., Bai, Y., Huang, S., Zheng, D., Liang, W., She, S., Peng, X., Wang, P., Mo, X., Song, Q., Lv, P., Huang, J., Ye, R. D., Wang, Y. FAM19A1 is a new ligand for GPR1 that modulates neural stem-cell proliferation and differentiation.

Entities:  

Keywords:  GPCR; cytokines; neural stem cell

Year:  2018        PMID: 29799787     DOI: 10.1096/fj.201800020RRR

Source DB:  PubMed          Journal:  FASEB J        ISSN: 0892-6638            Impact factor:   5.191


  7 in total

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Journal:  Front Cell Neurosci       Date:  2022-05-24       Impact factor: 6.147

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3.  Deorphanizing FAM19A proteins as pan-neurexin ligands with an unusual biosynthetic binding mechanism.

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Journal:  J Cell Biol       Date:  2020-09-07       Impact factor: 10.539

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Journal:  Mol Med Rep       Date:  2019-10-02       Impact factor: 2.952

5.  Single-nucleus characterization of adult mouse spinal dynorphin-lineage cells and identification of persistent transcriptional effects of neonatal hindpaw incision.

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6.  Age patterns of intra-pair DNA methylation discordance in twins: Sex difference in epigenomic instability and implication on survival.

Authors:  Qihua Tan; Shuxia Li; Mette Sørensen; Marianne Nygaard; Jonas Mengel-From; Kaare Christensen
Journal:  Aging Cell       Date:  2021-08-24       Impact factor: 9.304

7.  Ligand-binding and -scavenging of the chemerin receptor GPR1.

Authors:  Tobias F Fischer; Anne S Czerniak; Tina Weiß; Clara T Schoeder; Philipp Wolf; Oliver Seitz; Jens Meiler; Annette G Beck-Sickinger
Journal:  Cell Mol Life Sci       Date:  2021-07-09       Impact factor: 9.261

  7 in total

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