Unusual expression of human lymphocyte antigen class II in normal renal microvascular endothelium

Citation
Ka. Muczynski et al., Unusual expression of human lymphocyte antigen class II in normal renal microvascular endothelium, KIDNEY INT, 59(2), 2001, pp. 488-497
Citations number
59
Categorie Soggetti
Urology & Nephrology","da verificare
Journal title
KIDNEY INTERNATIONAL
ISSN journal
00852538 → ACNP
Volume
59
Issue
2
Year of publication
2001
Pages
488 - 497
Database
ISI
SICI code
0085-2538(200102)59:2<488:UEOHLA>2.0.ZU;2-2
Abstract
Background. The human lymphocyte antigen (HLA) class II proteins (DR, Do, a nd DP) and DM, a protein involved in loading antigenic peptide onto the cla ss II molecules, have a coordinate regulation that facilitates antigen pres entation to CD4+ T cells. CIITA is a specific transcription factor responsi ble for the coordinate regulation of these genes. DR expression in the kidn ey was described to be constitutive on renal microvascular endothelium in t he early 1980s. but expression of other genes involved in class II antigen presentation (DQ, DP, DM, and CIITA) has not been characterized. Methods. Expression of the HLA class II proteins. DM. and CIITA in normal h uman kidney cortex was evaluated by immunofluorescence microscopy, Northern blots, and reverse transcriptase-polymerase chain reaction (RT-PCR). Results. The endothelium of glomerular and peritubular capillaries constitu tively express DR, as indicated by colocalization of DR and CD31 antibodies . However. the endothelium of larger renal blood vessels is devoid of class II proteins. Capillaries that express DR do not have detectable Do, DP, or DM by immunofluorescence. Northern blots identified DR, DP. and DM mRNAs b ut not Do mRNA. CIITA was amplified by RT-PCR at a level that could account for the class II expressed by the microvascular endothelium. Conclusion. The renal microvascular endothelium constitutively expresses DR without the other class II proteins or DM. This discoordinate expression o f HLA class II genes is unusual and may contribute to the kidney's ability to control CD4+ T-cell responses.