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音猬因子信号分子在胚胎中脑多巴胺能神经元中的时空表达

Spatiotemporal expression of sonic hedgehog signalling molecules in the embryonic mesencephalic dopaminergic neurons.

作者信息

Hussein Manal T, Attaai Abdelraheim, Kamel Gamal, Mokhtar Doaa M

机构信息

Department of Anatomy and Histology, Faculty of Veterinary Medicine, Assiut University, Assiut, 71526, Egypt; Institute for Anatomy and Cell Biology, Department of Molecular Embryology, Faculty of Medicine, University of Freiburg, Freiburg, 79104, Germany.

Department of Anatomy and Histology, Faculty of Veterinary Medicine, Assiut University, Assiut, 71526, Egypt; Institute for Anatomy and Cell Biology, Department of Molecular Embryology, Faculty of Medicine, University of Freiburg, Freiburg, 79104, Germany; Faculty of Biology, University of Freiburg, Freiburg, 79104, Germany.

出版信息

Gene Expr Patterns. 2021 Dec;42:119217. doi: 10.1016/j.gep.2021.119217. Epub 2021 Nov 9.

Abstract

Midbrain dopaminergic neurons (mDA) play an important role in controlling the voluntary motor movement, reward, and emotion-based behaviour. Differentiation of mDA neurons from progenitors depends on several secreted proteins, such as sonic hedgehog (SHH). The present study attempted to elucidate the possible role(s) of some SHH signaling components (Ptch1, Gli1, Gli2 and Gli3) in the spatiotemporal development of mDA neurons along the rostrocaudal axis of the midbrain and their possible roles in differentiation and survival of mDA neurons and the significance of using in vitro models for studying the development of mDA neurons. At E12 and E14, only Ptch1 and Gli1 were expressed in ventrolateral midbrain domains. All examined SHH signalling molecules were not detected in mDA area. Whereas, in MN9D cells, many SHH signalling molecules were expressed and co-localized with the dopaminergic marker; tyrosine hydroxylase (TH), and their expression were upregulated with SHH treatment of the MN9D cells. These results suggest that mDA neurons differentiation and survival might be independent of SHH in the late developmental stages (E12-18). Besides, MN9D cell line is not the ideal in vitro model for investigating the differentiation of mDA and hence, the ventral midbrain primary culture might be favored over MN9D line.

摘要

中脑多巴胺能神经元(mDA)在控制自主运动、奖赏和基于情感的行为中发挥着重要作用。mDA神经元从祖细胞的分化依赖于多种分泌蛋白,如音猬因子(SHH)。本研究试图阐明一些SHH信号成分(Ptch1、Gli1、Gli2和Gli3)在中脑mDA神经元沿前后轴的时空发育中的可能作用,以及它们在mDA神经元分化和存活中的可能作用,以及使用体外模型研究mDA神经元发育的意义。在胚胎第12天(E12)和第14天(E14),只有Ptch1和Gli1在中脑腹外侧区域表达。在mDA区域未检测到所有检测的SHH信号分子。然而,在MN9D细胞中,许多SHH信号分子表达并与多巴胺能标志物酪氨酸羟化酶(TH)共定位,并且在MN9D细胞经SHH处理后它们的表达上调。这些结果表明,在发育后期(E12 - 18),mDA神经元的分化和存活可能独立于SHH。此外,MN9D细胞系不是研究mDA分化的理想体外模型,因此,腹侧中脑原代培养可能比MN9D细胞系更受青睐。

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