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成年斑马鱼大脑中低密度脂蛋白受体及其抑制剂前蛋白转化酶枯草溶菌素9的基因表达模式表明其在神经发生中可能发挥作用。

Gene expression patterns of the LDL receptor and its inhibitor Pcsk9 in the adult zebrafish brain suggest a possible role in neurogenesis.

作者信息

Gence Laura, Morello Elena, Rastegar Sepand, Apalama Marie Laurine, Meilhac Olivier, Bascands Jean-Loup, Diotel Nicolas

机构信息

Université de La Réunion, INSERM, UMR 1188, Diabète athérothrombose Thérapies Réunion Océan Indien (DéTROI), Saint-Pierre, La Réunion, France.

CHU de La Réunion, Saint-Pierre, La Réunion, France.

出版信息

Eur J Neurosci. 2025 Jan;61(1):e16586. doi: 10.1111/ejn.16586. Epub 2024 Nov 17.

DOI:10.1111/ejn.16586
PMID:39551948
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11664473/
Abstract

The low-density lipoprotein receptor (LDLr) is the first member of a closely related transmembrane protein family. It is known for its involvement in various physiological processes, mainly in the regulation of lipid metabolism, especially in the brains of mammals and zebrafish. In zebrafish, two ldlr genes (ldlra and b) have been identified and their distribution in the brain is not well documented. Recently, the roles of ldlr and its inhibitor pcsk9 in regenerative process after telencephalic brain injury have been discussed. In this study, we explored the expression patterns of these genes during zebrafish development. We found that ldlra expression was detected at the end of the pharyngula period (48 hpf) and increased during the larval stage. Conversely, ldlrb expression was observed from zygotic to larval stages. Using techniques like in situ hybridization and taking advantage of transgenic fish, we demonstrated the widespread distribution of ldlra, ldlrb and pcsk9 in the brain of adult zebrafish. Specifically, these genes were expressed in neurons and neural stem cells and also at lower levels in endothelial cells. As expected, intraperitoneal injection of fluorescent-labelled LDLs resulted in their uptake by cerebral endothelial cells in a homeostatic context, whereas they diffused within the brain parenchyma after telencephalic injury. However, after intracerebroventricular injections into animals, LDL particles were not taken up by neural stem cells. In conclusion, our results provide additional evidence for LDLr expression in the brain of adult zebrafish. These results raise the question of the role of LDLr in the cholesterol/lipid imbalance in cerebral complications.

摘要

低密度脂蛋白受体(LDLr)是一个密切相关的跨膜蛋白家族的首个成员。它因参与多种生理过程而闻名,主要是在脂质代谢的调节中,特别是在哺乳动物和斑马鱼的大脑中。在斑马鱼中,已鉴定出两个ldlr基因(ldlra和b),但其在大脑中的分布尚无充分记录。最近,人们讨论了ldlr及其抑制剂pcsk9在端脑损伤后再生过程中的作用。在本研究中,我们探究了这些基因在斑马鱼发育过程中的表达模式。我们发现,在咽胚期结束时(48小时胚胎期)可检测到ldlra的表达,且在幼体阶段表达增加。相反,从合子期到幼体阶段均可观察到ldlrb的表达。我们利用原位杂交等技术并借助转基因鱼,证明了ldlra、ldlrb和pcsk9在成年斑马鱼大脑中的广泛分布。具体而言,这些基因在神经元和神经干细胞中表达,在内皮细胞中的表达水平较低。正如预期的那样,在稳态情况下,腹腔注射荧光标记的低密度脂蛋白(LDLs)会导致其被脑内皮细胞摄取,而在端脑损伤后它们会在脑实质内扩散。然而,向动物脑室内注射后,LDL颗粒未被神经干细胞摄取。总之,我们的结果为成年斑马鱼大脑中LDLr的表达提供了更多证据。这些结果提出了LDLr在脑部并发症中胆固醇/脂质失衡中作用的问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef0d/11664473/b90d9b60e6b8/EJN-61-0-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef0d/11664473/9fd17f3fd694/EJN-61-0-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef0d/11664473/fa84ce6452a7/EJN-61-0-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef0d/11664473/0b68468c6a69/EJN-61-0-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef0d/11664473/e2ff97d6aeba/EJN-61-0-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef0d/11664473/dfe07b750d52/EJN-61-0-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef0d/11664473/bed38bf06fcf/EJN-61-0-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef0d/11664473/558ead2250b7/EJN-61-0-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef0d/11664473/0762e868084d/EJN-61-0-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef0d/11664473/b90d9b60e6b8/EJN-61-0-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef0d/11664473/9fd17f3fd694/EJN-61-0-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef0d/11664473/fa84ce6452a7/EJN-61-0-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef0d/11664473/0b68468c6a69/EJN-61-0-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef0d/11664473/e2ff97d6aeba/EJN-61-0-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef0d/11664473/dfe07b750d52/EJN-61-0-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef0d/11664473/bed38bf06fcf/EJN-61-0-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef0d/11664473/558ead2250b7/EJN-61-0-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef0d/11664473/0762e868084d/EJN-61-0-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef0d/11664473/b90d9b60e6b8/EJN-61-0-g001.jpg

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