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绘制未聚类原钙黏蛋白在发育中大脑中的组合表达图谱,确定新型 PCDH19 介导的细胞黏附特性。

Mapping combinatorial expression of non-clustered protocadherins in the developing brain identifies novel PCDH19-mediated cell adhesion properties.

机构信息

School of Biomedicine and Robinson Research Institute, University of Adelaide , Adelaide, South Australia 5005, Australia.

Genome Editing Program, South Australian Health and Medical Research Institute , Adelaide, South Australia 5000, Australia.

出版信息

Open Biol. 2024 Apr;14(4):230383. doi: 10.1098/rsob.230383. Epub 2024 Apr 17.

Abstract

Non-clustered protocadherins (ncPcdhs) are adhesive molecules with spatio-temporally regulated overlapping expression in the developing nervous system. Although their unique role in neurogenesis has been widely studied, their combinatorial role in brain physiology and pathology is poorly understood. Using probabilistic cell typing by sequencing, we demonstrate combinatorial inter- and intra-familial expression of ncPcdhs in the developing mouse cortex and hippocampus, at single-cell resolution. We discovered the combinatorial expression of Protocadherin-19 (), a protein involved in PCDH19-clustering epilepsy, with , or Cadherin 13 () in excitatory neurons. Using aggregation assays, we demonstrate a code-specific adhesion function of PCDH19; mosaic PCDH19 absence in PCDH19+9 and PCDH19 + CDH13, but not in PCDH19+1 codes, alters cell-cell interaction. Interestingly, we found that PCDH19 as a dominant protein in two heterophilic adhesion codes could promote -interaction between them. In addition, we discovered increased CDH13-mediated cell adhesion in the presence of PCDH19, suggesting a potential role of PCDH19 as an adhesion mediator of CDH13. Finally, we demonstrated novel -interactions between PCDH19 and PCDH1, PCDH9 and CDH13. These observations suggest that there is a unique combinatorial code with a cell- and region-specific characteristic where a single molecule defines the heterophilic cell-cell adhesion properties of each code.

摘要

非聚类原钙黏蛋白(ncPcdhs)是一种在神经系统发育过程中具有时空调节性重叠表达的黏附分子。尽管它们在神经发生中的独特作用已被广泛研究,但它们在大脑生理和病理中的组合作用仍知之甚少。我们通过测序的概率细胞分型,在单细胞分辨率下,证明了 ncPcdhs 在发育中的小鼠皮层和海马体中的细胞间和细胞内组合表达。我们发现了原钙黏蛋白 19()的组合表达,该蛋白与 PCDH19 聚类性癫痫有关,与兴奋性神经元中的或钙黏蛋白 13()组合表达。使用聚集测定法,我们证明了 PCDH19 的特定于代码的黏附功能;PCDH19 在 PCDH19+9 和 PCDH19+CDH13 中的缺失是马赛克型的,但不在 PCDH19+1 编码中,改变了细胞-细胞相互作用。有趣的是,我们发现 PCDH19 作为两种异源黏附代码中的主要蛋白,可以促进它们之间的相互作用。此外,我们发现 PCDH19 存在时 CDH13 介导的细胞黏附增加,这表明 PCDH19 可能作为 CDH13 的黏附介质发挥作用。最后,我们证明了 PCDH19 与 PCDH1、PCDH9 和 CDH13 之间存在新的相互作用。这些观察结果表明,存在一种具有细胞和区域特异性特征的独特组合代码,其中单个分子定义了每个代码的异源细胞-细胞黏附特性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf1a/11037505/7541d60fdd42/rsob.230383.f001.jpg

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