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发现维持驻留血管内皮干细胞特性的转录因子。

Discovery of Transcription Factors Involved in the Maintenance of Resident Vascular Endothelial Stem Cell Properties.

机构信息

Department of Signal Transduction, Research Institute for Microbial Diseases, Osaka University, Suita, Japan.

Laboratory of Signal Transduction, World Premier International Immunology Frontier Research Center, Osaka University, Suita, Japan.

出版信息

Mol Cell Biol. 2024 Jan;44(1):17-26. doi: 10.1080/10985549.2023.2297997. Epub 2024 Jan 29.

Abstract

A resident vascular endothelial stem cell (VESC) population expressing CD157 has been identified recently in mice. Herein, we identified transcription factors (TFs) regulating CD157 expression in endothelial cells (ECs) that were associated with drug resistance, angiogenesis, and EC proliferation. In the first screening, we detected 20 candidate TFs through the promoter and gene expression analyses. We found that 10 of the 20 TFs induced CD157 expression in ECs. We previously reported that 70% of CD157 VESCs were side population (SP) ECs that abundantly expressed ATP-binding cassette (ABC) transporters. Here, we found that the 10 TFs increased the expression of several ABC transporters in ECs and increased the proportion of SP ECs. Of these 10 TFs, we found that six (Atf3, Bhlhe40, Egr1, Egr2, Elf3, and Klf4) were involved in the manifestation of the SP phenotype. Furthermore, the six TFs enhanced tube formation and proliferation in ECs. Single-cell RNA sequence data in liver ECs suggested that Atf3 and Klf4 contributed to the production of CD157 VESCs in the postnatal period. We concluded that Klf4 might be important for the development and maintenance of liver VESCs. Our work suggests that a TF network is involved in the differentiation hierarchy of VESCs.

摘要

最近在小鼠中鉴定出一种表达 CD157 的常驻血管内皮干细胞 (VESC) 群体。在此,我们鉴定了与耐药性、血管生成和内皮细胞增殖相关的调节内皮细胞 (EC) 中 CD157 表达的转录因子 (TF)。在第一次筛选中,我们通过启动子和基因表达分析检测了 20 个候选 TF。我们发现这 20 个 TF 中有 10 个诱导 EC 中 CD157 的表达。我们之前报道过,70%的 CD157 VESCs 是侧群 (SP) ECs,它们大量表达 ATP 结合盒 (ABC) 转运体。在这里,我们发现这 10 个 TF 增加了 EC 中几种 ABC 转运体的表达,并增加了 SP ECs 的比例。在这 10 个 TF 中,我们发现其中 6 个 (Atf3、Bhlhe40、Egr1、Egr2、Elf3 和 Klf4) 参与了 SP 表型的表现。此外,这 6 个 TF 增强了 EC 中的管形成和增殖。肝 ECs 的单细胞 RNA 序列数据表明,Atf3 和 Klf4 有助于出生后 CD157 VESCs 的产生。我们得出结论,Klf4 可能对肝 VESCs 的发育和维持很重要。我们的工作表明,一个 TF 网络参与了 VESCs 的分化层次。

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