The Class I HLA Repertoire of Pancreatic Islets Comprises the Nonclassical Class Ib Antigen HLA-G

Author:

Cirulli Vincenzo1,Zalatan Jessie2,McMaster Michael3,Prinsen Robyn2,Salomon Daniel R.2,Ricordi Camillo4,Torbett Bruce E.2,Meda Paolo5,Crisa Laura2

Affiliation:

1. Whittier Institute for Diabetes, University of California San Diego, La Jolla, California

2. Department of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, California

3. Department of Cell and Tissue Biology, University of California San Francisco, San Francisco, California

4. Diabetes Research Institute, University of Miami School of Medicine, Miami, Florida

5. Department of Cell Physiology and Metabolism, University of Geneva, Geneva, Switzerland

Abstract

Selective expression of the human class Ib HLA molecule HLA-G in immunologically protected sites and its function in the inhibition of NK and T-cell effector functions support an important role of this molecule in immunoregulation. Here, we demonstrate that HLA-G is constitutively expressed in the endocrine compartment of the human pancreas. Surface expression of this HLA determinant in endocrine cells is regulated in response to growth and inflammatory stimuli. Furthermore, we provide evidence that HLA-G expressed in this tissue may associate with a subset of insulin-containing granules and may be shuttled to the cell surface in response to secretory stimuli. Thus, HLA-G presentation by endocrine cells may be regulated in concert with their secretory activity. These results identify the expression of a major histocompatibility complex locus with putative regulatory functions in human pancreatic islets, a finding with potentially important implications for the progression of autoimmunity as well as for the establishment of transplant tolerance to this tissue.

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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