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CC 趋化因子 CCL1 受体 CCR8 介导间充质干细胞向表达 FOXP3+CCR8+调节性 T 细胞的类胚体的转化。

CC chemokine CCL1 receptor CCR8 mediates conversion of mesenchymal stem cells to embryoid bodies expressing FOXP3+CCR8+ regulatory T cells.

机构信息

Department of Pathology, New York Medical College, Valhalla, NY, United States of America.

Department of Biological Sciences, New York City College of Technology, City University of New York, Brooklyn, NY, United States of America.

出版信息

PLoS One. 2019 Jul 17;14(7):e0218944. doi: 10.1371/journal.pone.0218944. eCollection 2019.

Abstract

Embryoid bodies (EBs) are three dimensional aggregates of pluripotent stem cells primarily used to investigate morphogenesis and cell toxicity, are also attractive tools in regenerative medicine. While embryonic stem cells (ESCs) and induced pluripotent cells (IPSCs) have been shown to form EBs in mouse, primate and humans, EB formation have not been previously demonstrated in mesenchymal stem cells (MSCs). Here we show that rat MSCs form EBs; which express regulatory T cell (Treg) marker Foxp3 and CC chemokine CCL1 receptor CCR8. We show a novel method for formation of EBs from MSCs under stress and demonstrate that the induction of FoxP3+ CCR8+ EBs is dependent upon CCL1 gradients which mediate cell proliferation, migration and invasion of mTregs. The identification of EBs and novel FoxP3+ CCR8+ regulatory T cells (mTregs) for selective conversion and isolation of bone marrow derived MSCs offers novel avenues for research, diagnosis and treatment.

摘要

胚状体(EBs)是多能干细胞的三维聚集物,主要用于研究形态发生和细胞毒性,在再生医学中也是很有吸引力的工具。虽然胚胎干细胞(ESCs)和诱导多能细胞(IPSCs)已在小鼠、灵长类动物和人类中显示出形成 EB 的能力,但间充质干细胞(MSCs)中尚未证明其能够形成 EB。在这里,我们展示了大鼠 MSCs 可以形成 EB;这些 EB 表达调节性 T 细胞(Treg)标记物 Foxp3 和 C 型趋化因子 CCL1 受体 CCR8。我们展示了一种在应激条件下从 MSCs 中形成 EB 的新方法,并证明 Foxp3+CCR8+EB 的诱导依赖于 CCL1 梯度,该梯度介导 mTregs 的细胞增殖、迁移和侵袭。EBs 和新型 Foxp3+CCR8+调节性 T 细胞(mTregs)的鉴定,为骨髓来源的 MSCs 的选择性转化和分离提供了新的途径,为研究、诊断和治疗开辟了新的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af4a/6636727/4f1ea834c4d9/pone.0218944.g001.jpg

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