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小GTP酶Arl8b的缺失导致小鼠胚胎顶板发育异常。

Loss of the small GTPase Arl8b results in abnormal development of the roof plate in mouse embryos.

作者信息

Hashimoto Keisuke, Yamaguchi Yoshifumi, Kishi Yusuke, Kikko Yorifumi, Takasaki Kanako, Maeda Yurie, Matsumoto Yudai, Oka Miho, Miura Masayuki, Ohata Shinya, Katada Toshiaki, Kontani Kenji

机构信息

Department of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.

Department of Biochemistry, Meiji Pharmaceutical University, Tokyo, Japan.

出版信息

Genes Cells. 2019 Jun;24(6):436-448. doi: 10.1111/gtc.12687. Epub 2019 May 26.

Abstract

Lysosomes are acidic organelles responsible for degrading both exogenous and endogenous materials. The small GTPase Arl8 localizes primarily to lysosomes and is involved in lysosomal function. In the present study, using Arl8b gene-trapped mutant (Arl8b ) mice, we show that Arl8b is required for the development of dorsal structures of the neural tube, including the thalamus and hippocampus. In embryonic day (E) 10.5 Arl8b embryos, Sox1 (a neuroepithelium marker) was ectopically expressed in the roof plate, whereas the expression of Gdf7 and Msx1 (roof plate markers) was reduced in the dorsal midline of the midbrain. Ectopic expression of Sox1 in Arl8b embryos was detected also at E9.0 in the neural fold, which gives rise to the roof plate. In addition, the levels of Bmp receptor IA and phosphorylated Smad 1/5/8 (downstream of BMP signaling) were increased in the neural fold of E9.0 Arl8b embryos. These results suggest that Arl8b is involved in the development of the neural fold and the subsequently formed roof plate, possibly via control of BMP signaling.

摘要

溶酶体是负责降解外源性和内源性物质的酸性细胞器。小GTP酶Arl8主要定位于溶酶体,并参与溶酶体功能。在本研究中,我们使用Arl8b基因捕获突变体(Arl8b-/-)小鼠,表明Arl8b是神经管背侧结构(包括丘脑和海马体)发育所必需的。在胚胎第10.5天(E10.5)的Arl8b-/-胚胎中,Sox1(一种神经上皮标志物)在顶板中异位表达,而Gdf7和Msx1(顶板标志物)在中脑背中线的表达减少。在Arl8b-/-胚胎中,Sox1的异位表达在E9.0时也在形成顶板的神经褶中被检测到。此外,在E9.0的Arl8b-/-胚胎的神经褶中,Bmp受体IA和磷酸化Smad 1/5/8(BMP信号的下游)水平升高。这些结果表明,Arl8b可能通过控制BMP信号参与神经褶和随后形成的顶板的发育。

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