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肾小球上皮蛋白-1在小鼠磨牙形态发生中的发育作用

Developmental roles of glomerular epithelial protein-1 in mice molar morphogenesis.

作者信息

Neupane Sanjiv, Aryal Yam Prasad, Kwak Hee-Jin, Lee Sung-Gwon, Kim Tae-Young, Pokharel Elina, Kim Ji-Youn, Kim Jung-Hyeuk, Sohn Wern-Joo, An Seo-Young, An Chang-Hyeon, Jung Jae-Kwang, Ha Jung-Hong, Yamamoto Hitoshi, Cho Sung-Won, Lee Sanggyu, Lee Youngkyun, Park Kwang-Kyun, Min Bong-Ki, Park Chungoo, Kwon Tae-Yub, Cho Sung-Jin, Kim Jae-Young

机构信息

Department of Biochemistry, School of Dentistry, Kyungpook National University, Daegu, Korea.

Department of Biochemistry and Cell Biology, Stony Brook University, Stony Brook, USA.

出版信息

Cell Tissue Res. 2024 Jan;395(1):53-62. doi: 10.1007/s00441-023-03841-y. Epub 2023 Nov 21.

Abstract

Glomerular epithelial protein-1 (Glepp1), a R3 subtype family of receptor-type protein tyrosine phosphatases, plays important role in the activation of Src family kinases and regulates cellular processes such as cell proliferation, differentiation, and apoptosis. In this study, we firstly examined the functional evaluation of Glepp1 in tooth development and morphogenesis. The precise expression level and developmental function of Glepp1 were examined by RT-qPCR, in situ hybridization, and loss and gain of functional study using a range of in vitro organ cultivation methods. Expression of Glepp1 was detected in the developing tooth germs in cap and bell stage of tooth development. Knocking down Glepp1 at E13 for 2 days showed the altered expression levels of tooth development-related signaling molecules, including Bmps, Dspp, Fgf4, Lef1, and Shh. Moreover, transient knock down of Glepp1 revealed alterations in cellular physiology, examined by the localization patterns of Ki67 and E-cadherin. Similarly, knocking down of Glepp1 showed disrupted enamel rod and interrod formation in 3-week renal transplanted teeth. In addition, due to attrition of odontoblastic layers, the expression signals of Dspp and the localization of NESTIN were almost not detected after knock down of Glepp1; however, their expressions were increased after Glepp1 overexpression. Thus, our results suggested that Glepp1 plays modulating roles during odontogenesis by regulating the expression levels of signaling molecules and cellular events to achieve the proper structural formation of hard tissue matrices in mice molar development.

摘要

肾小球上皮蛋白-1(Glepp1)是受体型蛋白酪氨酸磷酸酶R3亚型家族的一员,在Src家族激酶的激活中起重要作用,并调节细胞增殖、分化和凋亡等细胞过程。在本研究中,我们首先检测了Glepp1在牙齿发育和形态发生中的功能评估。通过RT-qPCR、原位杂交以及使用一系列体外器官培养方法进行功能的缺失和获得研究,检测了Glepp1的精确表达水平和发育功能。在牙齿发育的帽状期和钟状期的牙胚中检测到了Glepp1的表达。在E13期敲低Glepp1 2天,显示牙齿发育相关信号分子的表达水平发生改变,包括骨形态发生蛋白(Bmps)、牙本质涎磷蛋白(Dspp)、成纤维细胞生长因子4(Fgf4)、淋巴细胞增强因子1(Lef1)和音猬因子(Shh)。此外,短暂敲低Glepp1揭示了细胞生理学的改变,通过Ki67和E-钙黏蛋白的定位模式进行检测。同样,敲低Glepp1显示在3周龄肾移植牙中釉柱和柱间质形成受到破坏。此外,由于成牙本质细胞层的磨损,敲低Glepp1后几乎未检测到Dspp的表达信号和巢蛋白(NESTIN)的定位;然而,在Glepp1过表达后它们的表达增加。因此,我们的结果表明,Glepp1在小鼠磨牙发育过程中通过调节信号分子的表达水平和细胞事件,在牙发生过程中发挥调节作用,以实现硬组织基质的适当结构形成。

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