THE IMMUNOCHEMICAL DISTRIBUTION OF CYCLOPHILIN IN NORMAL MAMMALIAN TISSUES
- 1 August 1991
- journal article
- research article
- Published by Wolters Kluwer Health in Transplantation
- Vol. 52 (2) , 340-344
- https://doi.org/10.1097/00007890-199108000-00030
Abstract
Cyclophilin, a 17 Kd proline cis-trans isomerase, high-affinity (Kd 10–8 M) target for the immunosuppressive drug cyclosporine has ubiquitous phylogenic distribution, but its tissue localization in mammals has not been detailed. To explore a potential relationship between the multiple systemic effects of CsA and the cellular and tissue distribution of CYP, thirty-three different normal porcine tissues were examined using an immunohisto-chemical technique. Tissue was obtained from farm-bred pigs, immediately fixed in buffered formalin, and prepared as embedded 5-μ sections. Immune-specific staining was accomplished using an ABC immunoper-oxidase method and an affinity-purified, monospecific, rabbit anti-CYP IgG. Cut sections served as their own blanks and controls, and all tissues were stained in batch to minimize the effects of variation in technique. Consistent with earlier reports, CYP was present in all tissues studied, however, there was remarkable heterogeneity in CYP distribution. Renal parenchymal cells, cardiac and striated muscle, pulmonary and skin demonstrated cytoplasmic immunospecific CYP—however, the cellular localization varied. Cytoplasmic staining of endothelial, neural, and glandular elements was consistently observed. Contrasting with previous reports, CYP localized to the nucleus as well as the cytoplasm of some lymphoid cells, hepatocytes, and cells of the large intestine. Generally, greater CYP-specific staining was noted in organs amenable to CsA immunosuppression (heart, liver, kidney), compared with organs deemed more immunologically vulnerable when allografted under CsA (pancreas, lung, small bowel). Similarly, CYP-immunospecific staining was abundant in tissues susceptible to CsA toxicities (neural tissue, smooth muscle, kidney, liver). This detailed immunohistological examination.Keywords
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