Cargando…

Molecular Structure, Expression and Role of TAFA4 and its Receptor FPR1 in the Spinal Cord

TAFA chemokine like family member 4 (TAFA4, also named FAM19A4) is a member of the TAFA chemokine like ligand or FAM19A family, which includes TAFA1, TAFA2, TAFA3, TAFA4, and TAFA5 (or FAM19A1, FAM19A2, FAM19A3, FAM19A4, and FAM19A5). They are also referred to as neurokines and are involved in the r...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhu, Sipin, Hu, Xiaoyong, Bennett, Samuel, Mai, Yuliang, Xu, Jiake
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9194834/
https://www.ncbi.nlm.nih.gov/pubmed/35712659
http://dx.doi.org/10.3389/fcell.2022.911414
_version_ 1784726808713756672
author Zhu, Sipin
Hu, Xiaoyong
Bennett, Samuel
Mai, Yuliang
Xu, Jiake
author_facet Zhu, Sipin
Hu, Xiaoyong
Bennett, Samuel
Mai, Yuliang
Xu, Jiake
author_sort Zhu, Sipin
collection PubMed
description TAFA chemokine like family member 4 (TAFA4, also named FAM19A4) is a member of the TAFA chemokine like ligand or FAM19A family, which includes TAFA1, TAFA2, TAFA3, TAFA4, and TAFA5 (or FAM19A1, FAM19A2, FAM19A3, FAM19A4, and FAM19A5). They are also referred to as neurokines and are involved in the regulation of a diverse range of cellular processes, including chemotaxis of macrophages, phagocytosis, and release of reactive oxygen species (ROS). TAFA4 is a marker of C-low-threshold mechanoreceptors and is expressed predominantly in nociceptors, such as dorsal root ganglia (DRG). TAFA4 has been implicated in the sensory perception of pain in the spinal cord. Mice with deficiency of TAFA4 demonstrate altered excitability in lamina IIi neurons in DRG in addition to increased mechanical and chemical nociception following inflammation or injury. As a secreted protein, TAFA4 binds to cell surface receptor formyl peptide receptor 1 (FPR1), a G protein-coupled receptor to mediate the chemoattraction of macrophages, phagocytosis, and the inflammatory profile of macrophages. It also interacts with cell surface neurexin to mediate signalling across the synapse. Further understanding the mechanisms by which this conserved protein family regulates diverse biological processes such as in neuronal functions, inflammation, and tissue fibrosis will help to design therapeutic targets for the treatment of TAFA related diseases such as spinal cord injury and neuro-inflammatory disorders.
format Online
Article
Text
id pubmed-9194834
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-91948342022-06-15 Molecular Structure, Expression and Role of TAFA4 and its Receptor FPR1 in the Spinal Cord Zhu, Sipin Hu, Xiaoyong Bennett, Samuel Mai, Yuliang Xu, Jiake Front Cell Dev Biol Cell and Developmental Biology TAFA chemokine like family member 4 (TAFA4, also named FAM19A4) is a member of the TAFA chemokine like ligand or FAM19A family, which includes TAFA1, TAFA2, TAFA3, TAFA4, and TAFA5 (or FAM19A1, FAM19A2, FAM19A3, FAM19A4, and FAM19A5). They are also referred to as neurokines and are involved in the regulation of a diverse range of cellular processes, including chemotaxis of macrophages, phagocytosis, and release of reactive oxygen species (ROS). TAFA4 is a marker of C-low-threshold mechanoreceptors and is expressed predominantly in nociceptors, such as dorsal root ganglia (DRG). TAFA4 has been implicated in the sensory perception of pain in the spinal cord. Mice with deficiency of TAFA4 demonstrate altered excitability in lamina IIi neurons in DRG in addition to increased mechanical and chemical nociception following inflammation or injury. As a secreted protein, TAFA4 binds to cell surface receptor formyl peptide receptor 1 (FPR1), a G protein-coupled receptor to mediate the chemoattraction of macrophages, phagocytosis, and the inflammatory profile of macrophages. It also interacts with cell surface neurexin to mediate signalling across the synapse. Further understanding the mechanisms by which this conserved protein family regulates diverse biological processes such as in neuronal functions, inflammation, and tissue fibrosis will help to design therapeutic targets for the treatment of TAFA related diseases such as spinal cord injury and neuro-inflammatory disorders. Frontiers Media S.A. 2022-05-31 /pmc/articles/PMC9194834/ /pubmed/35712659 http://dx.doi.org/10.3389/fcell.2022.911414 Text en Copyright © 2022 Zhu, Hu, Bennett, Mai and Xu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Zhu, Sipin
Hu, Xiaoyong
Bennett, Samuel
Mai, Yuliang
Xu, Jiake
Molecular Structure, Expression and Role of TAFA4 and its Receptor FPR1 in the Spinal Cord
title Molecular Structure, Expression and Role of TAFA4 and its Receptor FPR1 in the Spinal Cord
title_full Molecular Structure, Expression and Role of TAFA4 and its Receptor FPR1 in the Spinal Cord
title_fullStr Molecular Structure, Expression and Role of TAFA4 and its Receptor FPR1 in the Spinal Cord
title_full_unstemmed Molecular Structure, Expression and Role of TAFA4 and its Receptor FPR1 in the Spinal Cord
title_short Molecular Structure, Expression and Role of TAFA4 and its Receptor FPR1 in the Spinal Cord
title_sort molecular structure, expression and role of tafa4 and its receptor fpr1 in the spinal cord
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9194834/
https://www.ncbi.nlm.nih.gov/pubmed/35712659
http://dx.doi.org/10.3389/fcell.2022.911414
work_keys_str_mv AT zhusipin molecularstructureexpressionandroleoftafa4anditsreceptorfpr1inthespinalcord
AT huxiaoyong molecularstructureexpressionandroleoftafa4anditsreceptorfpr1inthespinalcord
AT bennettsamuel molecularstructureexpressionandroleoftafa4anditsreceptorfpr1inthespinalcord
AT maiyuliang molecularstructureexpressionandroleoftafa4anditsreceptorfpr1inthespinalcord
AT xujiake molecularstructureexpressionandroleoftafa4anditsreceptorfpr1inthespinalcord