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Notch 信号的时间调控及其对培养的角膜缘上皮细胞分化的影响。

Temporal Regulation of Notch Signaling and Its Influence on the Differentiation of Cultured Limbal Epithelial Cells.

机构信息

Stem Cell Research Lab, GROW Laboratory, Narayana Nethralaya Foundation, Bangalore, Karnataka, India.

Department of Cornea and Refractive Surgery, Narayana Nethralaya Eye Hospital, Bangalore, Karnataka, India.

出版信息

Curr Eye Res. 2020 Apr;45(4):459-470. doi: 10.1080/02713683.2019.1673436. Epub 2019 Oct 8.

Abstract

: Notch signaling plays a vital role in the differentiation and proliferation of corneal epithelial cells from limbal stem cells. The temporal regulation of Notch signaling during this differentiation remains unknown. Hence, we investigated the importance of temporal activation/blockage of Notch signaling during corneal differentiation.: Human limbal epithelial cultures were established with and without Notch activators (rec-Human Jagged1 Fc chimera) and pharmacological blockers (LY-411575). The modulation of Notch signaling was done at different time points during cell differentiation, which were collected on Day 14 for further analysis of differentiation, proliferation, maturation and apoptosis using RT-qPCR and immunofluorescence staining.: The activation of Notch signaling at Day 8 resulted in the highest number of mature corneal epithelial cells ( = .008) and pro-apoptosis marker BAX ( = .0001) with no increase in the number of corneal progenitors, and proliferation marker Ki67 compared to untreated controls. Cultures grown in the presence of Notch signaling blockers showed a significantly higher number of corneal progenitors ( = .0001) and proliferation marker Ki67 ( = .02) but lower corneal epithelial marker CK3/CK12 ( = .0007) and no difference in the pro-apoptotic marker BAX compared to untreated controls.: During the differentiation of limbal epithelial cells to the corneal epithelial cell type, Day 8 seems to be a crucial window to modulate Notch signaling for a customized outcome.

摘要

Notch 信号通路在角膜缘干细胞分化和增殖为角膜上皮细胞的过程中起着至关重要的作用。然而, Notch 信号通路在这一分化过程中的时间调控仍然未知。因此,我们研究了 Notch 信号在角膜分化过程中时间激活/阻断的重要性。

建立了含有和不含有 Notch 激活剂(重组人 Jagged1 Fc 嵌合体)和药理学抑制剂(LY-411575)的人角膜缘上皮细胞培养物。 Notch 信号的调制在细胞分化的不同时间点进行,在第 14 天收集细胞进行进一步的分化、增殖、成熟和凋亡分析,采用 RT-qPCR 和免疫荧光染色。

在第 8 天激活 Notch 信号通路导致成熟的角膜上皮细胞数量最多( =.008)和促凋亡标志物 BAX( =.0001),与未处理的对照组相比,角膜祖细胞和增殖标志物 Ki67 没有增加。与未处理的对照组相比,在 Notch 信号通路抑制剂存在的情况下培养的细胞显示出更高数量的角膜祖细胞( =.0001)和增殖标志物 Ki67( =.02),但角膜上皮标志物 CK3/CK12( =.0007)较低,促凋亡标志物 BAX 没有差异。

在角膜缘上皮细胞向角膜上皮细胞类型分化的过程中,第 8 天似乎是一个调节 Notch 信号以获得定制结果的关键窗口。

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