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

Author:

Johnson Ben1234ORCID,Iuliano Maria1536ORCID,Lam TuKiet T.78ORCID,Biederer Thomas153ORCID,De Camilli Pietro V.1234ORCID

Affiliation:

1. Yale University School of Medicine 1 Department of Neuroscience, , New Haven, CT, USA

2. Yale University School of Medicine 2 Department of Cell Biology, , New Haven, CT, USA

3. Yale University School of Medicine 5 Program in Cellular Neuroscience, Neurodegeneration and Repair, , New Haven, CT, USA

4. Yale University School of Medicine 6 Howard Hughes Medical Institute, , New Haven, CT, USA

5. Yale University School of Medicine 3 Department of Neurology, , New Haven, CT, USA

6. Tufts University School of Medicine 8 Department of Neuroscience, , Boston, MA, USA

7. Yale University School of Medicine 4 Department of Molecular Biophysics and Biochemistry, , New Haven, CT, USA

8. Yale University School of Medicine 7 Department of Keck MS and Proteomics Resource, , New Haven, CT, USA

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.

Funder

National Institutes of Health

Kavli Institute for Neuroscience

Yale School of Medicine

Publisher

Rockefeller University Press

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3