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鉴定定义人多能干细胞衍生的 PRRX1+肢芽样间充质细胞的表面抗原。

Identification of Surface Antigens That Define Human Pluripotent Stem Cell-Derived PRRX1+Limb-Bud-like Mesenchymal Cells.

机构信息

Department of Regenerative Science, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine, Okayama 700-8558, Japan.

Precision Health, Department of Bioengineering, Graduate School of Engineering, The University of Tokyo, Tokyo 113-8656, Japan.

出版信息

Int J Mol Sci. 2022 Feb 28;23(5):2661. doi: 10.3390/ijms23052661.

DOI:10.3390/ijms23052661
PMID:35269809
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8910499/
Abstract

Stem cell-based therapies and experimental methods rely on efficient induction of human pluripotent stem cells (hPSCs). During limb development, the lateral plate mesoderm (LPM) produces limb-bud mesenchymal (LBM) cells that differentiate into osteochondroprogenitor cells and form cartilage tissues in the appendicular skeleton. Previously, we generated PRRX1-tdTomato reporter hPSCs to establish the protocol for inducing the hPSC-derived PRRX1 LBM-like cells. However, surface antigens that assess the induction efficiency of hPSC-derived PRRX1 LBM-like cells from LPM have not been identified. Here, we used PRRX1-tdTomato reporter hPSCs and found that high pluripotent cell density suppressed the expression of mRNA and tdTomato after LBM-like induction. RNA sequencing and flow cytometry suggested that PRRX1-tdTomato LBM-like cells are defined as CD44 CD140B CD49f. Importantly, other hPSC lines, including four human induced pluripotent stem cell lines (414C2, 1383D2, HPS1042, HPS1043) and two human embryonic stem cell lines (SEES4, SEES7), showed the same results. Thus, an appropriate cell density of hPSCs before differentiation is a prerequisite for inducing the CD44 CD140B CD49f PRRX1 LBM-like cells.

摘要

基于干细胞的疗法和实验方法依赖于高效诱导人多能干细胞(hPSC)。在肢体发育过程中,侧板中胚层(LPM)产生肢芽间质(LBM)细胞,这些细胞分化为成骨软骨祖细胞,并在附肢骨骼中形成软骨组织。以前,我们生成了 PRRX1-tdTomato 报告 hPSC,以建立诱导 hPSC 衍生的 PRRX1 LBM 样细胞的方案。然而,评估 hPSC 衍生的 PRRX1 LBM 样细胞从 LPM 诱导效率的表面抗原尚未确定。在这里,我们使用了 PRRX1-tdTomato 报告 hPSC,并发现高多能细胞密度抑制了 LBM 样诱导后 mRNA 和 tdTomato 的表达。RNA 测序和流式细胞术表明,PRRX1-tdTomato LBM 样细胞被定义为 CD44 CD140B CD49f。重要的是,其他 hPSC 系,包括四个人类诱导多能干细胞系(414C2、1383D2、HPS1042、HPS1043)和两个人类胚胎干细胞系(SEES4、SEES7),也显示出相同的结果。因此,在分化前 hPSC 的适当细胞密度是诱导 CD44 CD140B CD49f PRRX1 LBM 样细胞的前提条件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3abe/8910499/d3e6afc00e7c/ijms-23-02661-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3abe/8910499/b72c5a239fe3/ijms-23-02661-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3abe/8910499/8581bace6445/ijms-23-02661-g002a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3abe/8910499/646cdeab4fff/ijms-23-02661-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3abe/8910499/d3e6afc00e7c/ijms-23-02661-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3abe/8910499/b72c5a239fe3/ijms-23-02661-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3abe/8910499/8581bace6445/ijms-23-02661-g002a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3abe/8910499/646cdeab4fff/ijms-23-02661-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3abe/8910499/d3e6afc00e7c/ijms-23-02661-g004.jpg

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本文引用的文献

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Induction and expansion of human PRRX1 limb-bud-like mesenchymal cells from pluripotent stem cells.
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