Astrocytes promote oligodendrocyte precursor cell proliferation via Cx47-mediated regulation of exosome-derived CHI3L1 secretion.
10.11817/j.issn.1672-7347.2025.240542
- Author:
Xiaoyan ZHANG
1
,
2
;
Nannan CHENG
3
;
Yan PENG
4
Author Information
1. Laboratory of Stem Cell and Tissue Engineering, Department of Histology and Embryology, Chongqing Medical University, Chongqing 400016, China. xxxxxiaoyy@
2. com.
3. Laboratory of Stem Cell and Tissue Engineering, Department of Histology and Embryology, Chongqing Medical University, Chongqing 400016, China.
4. Laboratory of Stem Cell and Tissue Engineering, Department of Histology and Embryology, Chongqing Medical University, Chongqing 400016, China. 100433@cqmu.edu.cn.
- Publication Type:Journal Article
- Keywords:
5-ethynyl-2'-deoxyuridine;
astrocytes;
cell proliferation;
chitinase-3-like protein 1;
connexin 47;
differentially expressed genes;
exosomes;
oligodendrocyte precursor cells;
transcriptome sequencing
- MeSH:
Animals;
Exosomes/metabolism*;
Cell Proliferation;
Rats, Sprague-Dawley;
Rats;
Connexins/genetics*;
Oligodendrocyte Precursor Cells/metabolism*;
Astrocytes/metabolism*;
Chitinase-3-Like Protein 1/metabolism*;
Cells, Cultured;
Cell Differentiation
- From:
Journal of Central South University(Medical Sciences)
2025;50(4):573-585
- CountryChina
- Language:English
-
Abstract:
OBJECTIVES:Neurodegenerative diseases are closely associated with myelin loss, and the proliferation and differentiation of oligodendrocyte precursor cells (OPCs) are crucial to remyelination. However, the regulatory mechanisms involved remain incompletely understood. This study aims to investigate how astrocytes (ASTs) regulate the secretion of chitinase-3-like protein 1 (CHI3L1) via connexin 47 (Cx47)-mediated exosome signaling, and its subsequent effect on OPC proliferation.
METHODS:Primary cells were isolated from postnatal day 1 Sprague-Dawley (P1SD) rats to establish 3 culture conditions: OPCs alone (Group O), OPCs in direct contact with ASTs (Group C), and OPCs cultured with AST-conditioned medium (Group A). Cellular morphology and proliferation were assessed using optical microscopy, 5-ethynyl-2'- deoxyuridine (EdU) incorporation, and flow cytometry. RNA sequencing (RNA-Seq) and bioinformatics analysis (BA) were conducted to identify differentially expressed genes (DEGs) among groups. Protein expression and cell cycle distribution were analyzed by Western blotting (WB) and flow cytometry. Exosomes were isolated and purified via differential centrifugation, characterized by nanoparticle tracking analysis (NTA) and transmission electron microscopy (TEM), and CHI3L1 expression in exosomes was verified via WB. Cx47 was silenced using small interfering RNA (siRNA) to evaluate its effect on OPC proliferation and exosome secretion. Artificial exosomes were constructed by encapsulating CHI3L1 in single unilamellar vesicles (SUVs), whose structure and size were validated by NTA and TEM. Following Cx47 knockdown, artificial exosomes were added back, and OPC proliferation was assessed via flow cytometry and EdU assay.
RESULTS:Direct co-cultured with ASTs (Group C) resulted in significantly enhanced OPC proliferation compared to the Group O and Group A (P<0.05). RNA-Seq and WB analyses revealed that ASTs promote OPC proliferation and exosome secretion enriched in CHI3L1 through Cx47. Cx47 knockdown by siRNA led to significant decreases in OPC proliferation and exosome release (P<0.05). The inhibitory effect of Cx47 silencing on OPC proliferation was partially reversed by supplementation with either isolated exosomes or exogenous CHI3L1.
CONCLUSIONS:This study reveals a novel mechanism by which ASTs regulate OPC proliferation: Through direct contact, ASTs enhance the secretion of CHI3L1-rich exosomes via Cx47, thereby converting intercellular contact signals into secretory signals that promote OPC proliferation. As a key exosomal molecule, CHI3L1 may play an important role in neural function and remyelination and warrants further investigation.
