Differential regulation of calcineurin isoforms in transplant patients: A new look at an old problem

Document Type

Article

Publication Date

2013

Abstract

Background: Calcineurin is a ubiquitously expressed calcium-dependent phosphatase that is inhibited by the immunosuppressant drugs cyclosporine and tacrolimus. Measuring calcineurin activity in transplant patients has been complicated by a lack of consistent correlation between drug level and enzyme activity, particularly with chronic use. Data from mice lacking the CnAα or CnAß isoform of the catalytic subunit of calcineurin demonstrate that loss of CnAß results in immunosuppression, whereas loss of CnAα does not. As such, methods to examine activity of the CnAß isoform may be more clinically relevant than nonspecific assays. Methods: Because the current enzyme assays are nonisoform specific, we examined association of the CnAα or CnAß isoform with calmodulin (CaM), a shared binding protein that is only associated with the catalytic subunit in the presence of calcium. We then compared semiquantitated data with total calcineurin activity and immune status in a cohort of pretransplantation controls and postrenal transplantation patients. Results: We found no difference in calcineurin activity between the groups and no difference in the amount of non-isoform-specific catalytic subunit bound to CaM. However, association of CnAα-CaM is increased in transplant patients, whereas CnAß-CaM is decreased. In addition, the amount of CnAß-CaM corresponds positively with T-cell activity and negatively with tacrolimus level. Finally, CnAß-CaM is lower in stable transplant patients compared with those with acute rejection. Conclusions: These data suggest that monitoring specifically the ß isoform may be more informative than non-isoform-specific assay methods.

Publication Title

Transplantation

Volume

96

Issue

3

First Page

239

Last Page

244

Comments

This article was published in Transplantation, Volume 96, Issue 3, Pages 239-244.

The published version is available at http://dx.doi.org/10.1097/TP.0b013e31829acb64.

Copyright © 2013 LWW.

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