Editing of CD1d-Bound Lipid Antigens by Endosomal Lipid Transfer Proteins

Author:

Zhou Dapeng12345,Cantu Carlos12345,Sagiv Yuval12345,Schrantz Nicolas12345,Kulkarni Ashok B.12345,Qi Xiaoyang12345,Mahuran Don J.12345,Morales Carlos R.12345,Grabowski Gregory A.12345,Benlagha Kamel12345,Savage Paul12345,Bendelac Albert12345,Teyton Luc12345

Affiliation:

1. Department of Pathology, University of Chicago, Chicago, IL 60637, USA.

2. Department of Immunology, Scripps Research Institute, La Jolla, CA 92037, USA.

3. National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892, USA.

4. Children Hospital Medical Center, Cincinnati, OH 45229–3039, USA.

5. Department of Medicine and Pathobiology, University of Toronto, Toronto, ON M5G 1X8, Canada.

Abstract

It is now established that CD1 molecules present lipid antigens to T cells, although it is not clear how the exchange of lipids between membrane compartments and the CD1 binding groove is assisted. We report that mice deficient in prosaposin, the precursor to a family of endosomal lipid transfer proteins (LTP), exhibit specific defects in CD1d-mediated antigen presentation and lack Vα14 NKT cells. In vitro, saposins extracted monomeric lipids from membranes and from CD1, thereby promoting the loading as well as the editing of lipids on CD1. Transient complexes between CD1, lipid, and LTP suggested a “tug-of-war” model in which lipid exchange between CD1 and LTP is on the basis of their respective affinities for lipids. LTPs constitute a previously unknown link between lipid metabolism and immunity and are likely to exert a profound influence on the repertoire of self, tumor, and microbial lipid antigens.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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