Analysis of the cDNA sequence encoding MHC-Aβ in tubular epithelium from mouse kidney View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

1991-07

AUTHORS

Shelley E. Albert, Kathleen Shelton, Mae Jane Sun, Eric G. Neilson

ABSTRACT

Class II gene products of the major histocompatibility complex (MHC) are not expressed usually in abundance on normal epithelium. The cell surface visibility of such proteins for the immune system is thought to be limited protectively in order to minimize inflammation consequent to the recognition of self-antigens in parenchymal structures by T lymphocytes. In the current experiments we investigated whether the previously recognized sparseness of A beta on the surface of tubular epithelial cells might be accounted for by a protein coding difference deduced from the primary structure of its transcript compared with sequence from lymphoid cells that normally express A beta in generous amounts. We demonstrate, however, using clones obtained from a cDNA library prepared from tubular epithelium harvested from H-2s (A beta/alpha+; E beta/alpha-) mice susceptible to autoimmune interstitial nephritis, that the nucleotide sequence encoding the class II A beta chain in cells from both compartments is essentially identical. Our findings suggest that there is no primary structural aberrancy in the coding region of parenchymal A beta that would contribute to its low expression. The protective tolerance afforded by reduced numbers of class II molecules in normal tissues is, therefore, more likely the result of repressive regulatory processes. More... »

PAGES

139-142

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/ki.1991.191

DOI

http://dx.doi.org/10.1038/ki.1991.191

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1032943285

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/1921150


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