外泌体递送miRNA-323-3p参与先天性巨结肠症的发生

核心信息

  • 论文英文标题: Exosome-transmitted microRNA-323a-3p participated in the occurrence of Hirschsprung's disease
  • 期刊: Epigenomics
  • 发表年份: 2026
  • DOI: 10.1080/17501911.2026.2647714
  • PMID/PMCID: 41906498; PMC13097784

研究概览

We assessed the effects of exosomal miR-323a-3p on the proliferation and migration of immortalized ENCC-derived neural cell line (iENC) in vitro using CCK-8, EdU and Transwell assays, and its impact on ENCC migration in vivo using a zebrafish model. Our results suggest that measuring plasma exosomal miR-323a-3p in blood could help doctors diagnose HSCR earlier and that the miR-323a-3p/TET2 pathway may be a target for future treatments.

核心发现

Exosomal miR-323a-3p was taken up by iENCs and suppressed their proliferation and migration.

TET2 was identified as a potential miR-323a-3p target.

TET2 was downregulated in HSCR aganglionic tissues, and its knockdown inhibited iENC proliferation and migration.

In the zebrafish model, exosomal miR-323a-3p impaired distal ENCC colonization.

研究设计

Plasma exosomes and colon tissues were collected from HSCR patients and controls.

We assessed the effects of exosomal miR-323a-3p on the proliferation and migration of immortalized ENCC-derived neural cell line (iENC) in vitro using CCK-8, EdU and Transwell assays, and its impact on ENCC migration in vivo using a zebrafish model.

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关联平台: Exoomics®, Research Reagents & Tools

关联服务与能力: EV Isolation & Purification, Research Reagent / Product Supply

关联产品或试剂: Exosupur® EV Isolation/Purification Kit

参考文献

原始论文: Exosome-transmitted microRNA-323a-3p participated in the occurrence of Hirschsprung's disease Epigenomics. 2026. DOI: 10.1080/17501911.2026.2647714. PMID/PMCID: 41906498; PMC13097784.