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Reelin蛋白和mDab1蛋白调节海马体连接的发育。

Reelin and mDab1 regulate the development of hippocampal connections.

作者信息

Borrell Victor, Pujadas Lluís, Simó Sergi, Durà David, Solé Marta, Cooper Jonathan A, Del Río Jose A, Soriano Eduardo

机构信息

Developmental Neurobiology and Regeneration Laboratory, Institute for Research in Biomedicine (IRB)-Barcelona Science Park, Barcelona, E-08028, Spain.

出版信息

Mol Cell Neurosci. 2007 Oct;36(2):158-73. doi: 10.1016/j.mcn.2007.06.006. Epub 2007 Jul 18.

Abstract

We analyze in this study the participation of Reelin and mDab1 in the development of hippocampal connections. We show that mDab1 is present in growth cones and axonal tracts of developing hippocampal afferents. mdab1-deficiency produces severe alterations in the entorhino-hippocampal and commissural connections identical to those described in reeler mice, including innervation of ectopic areas, formation of abnormal patches of fiber termination and a delay in the refinement of projections. Organotypic slice cultures combining tissue from mdab1-mutant and control mice demonstrate that the abnormalities observed in the mutant entorhino-hippocampal projection are caused by mdab1-deficiency in both the projecting neurons and target hippocampal cells. Axonal afferents that innervate the hippocampus react to Reelin by reducing axonal growth, and increasing growth cone collapse and axonal branching. Altogether these results indicate that Reelin and mDab1 participate in the development and refinement of hippocampal connections by regulating axonal extension, targeting and branching.

摘要

在本研究中,我们分析了Reelin和mDab1在海马体连接发育中的作用。我们发现mDab1存在于发育中的海马体传入神经的生长锥和轴突束中。mdab1基因缺失会导致内嗅皮质-海马体和连合连接出现严重改变,与reeler小鼠中描述的情况相同,包括异位区域的神经支配、纤维终末异常斑块的形成以及投射细化延迟。将mdab1突变小鼠和对照小鼠的组织进行联合培养的器官型切片显示,突变的内嗅皮质-海马体投射中观察到的异常是由投射神经元和靶海马体细胞中的mdab1基因缺失引起的。支配海马体的轴突传入神经对Reelin产生反应,表现为轴突生长减少、生长锥塌陷增加和轴突分支增加。这些结果共同表明,Reelin和mDab1通过调节轴突延伸、靶向和分支参与海马体连接的发育和细化。

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