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细胞间接触处的脂质转运内质网蛋白 TMEM24 和 C2CD2 与带 4.1 的复合物。

A complex of the lipid transport ER proteins TMEM24 and C2CD2 with band 4.1 at cell-cell contacts.

机构信息

Department of Neuroscience, Yale University School of Medicine, New Haven, CT, USA.

Department of Cell Biology, Yale University School of Medicine, New Haven, CT, USA.

出版信息

J Cell Biol. 2024 Nov 4;223(11). doi: 10.1083/jcb.202311137. Epub 2024 Aug 19.

Abstract

Junctions between the ER and plasma membrane (PM) are implicated in calcium homeostasis, non-vesicular lipid transfer, and other cellular functions. Two ER proteins that function both as tethers to the PM via a polybasic C-terminus motif and as phospholipid transporters are brain-enriched TMEM24 (C2CD2L) and its paralog C2CD2. We report that both proteins also form a complex with band 4.1 family members, which in turn bind PM proteins including cell adhesion molecules such as SynCAM 1. This complex enriches TMEM24 and C2CD2 containing ER/PM junctions at sites of cell contacts. Dynamic properties of TMEM24-dependent ER/PM junctions are impacted when band 4.1 is part of the junction, as TMEM24 at cell-adjacent ER/PM junctions is not shed from the PM by calcium rise, unlike TMEM24 at non-cell adjacent junctions. Lipid transport between the ER and the PM by TMEM24 and C2CD2 at sites where cells, including neurons, contact other cells may participate in adaptive responses to cell contact-dependent signaling.

摘要

内质网 (ER) 和质膜 (PM) 之间的连接与钙稳态、非囊泡脂质转移和其他细胞功能有关。两种内质网蛋白通过多碱性 C 端基序作为质膜的连接蛋白,并作为磷脂转运蛋白发挥作用,分别是脑丰富的 TMEM24(C2CD2L)及其同源物 C2CD2。我们报告这两种蛋白也与带 4.1 家族成员形成复合物,而带 4.1 家族成员又与包括细胞粘附分子如 SynCAM 1 在内的质膜蛋白结合。该复合物在细胞接触部位富集包含 TMEM24 和 C2CD2 的 ER/PM 连接。当带 4.1 是连接的一部分时,TMEM24 依赖性 ER/PM 连接的动态特性受到影响,因为与非细胞相邻连接相比,细胞相邻 ER/PM 连接处的 TMEM24 不会因钙升高而从质膜脱落。TMEM24 和 C2CD2 在包括神经元在内的与其他细胞接触的细胞处的 ER 和 PM 之间的脂质转运可能参与细胞接触依赖性信号的适应性反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9757/11334333/298b86a040bb/JCB_202311137_Fig1.jpg

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