Glomerular mRNA expression of prothrombotic and antithrombotic factors in renal transplants with thrombotic microangiopathy
PA Agustian, CL Bockmeyer, F Modde, J Wittig… - …, 2013 - journals.lww.com
PA Agustian, CL Bockmeyer, F Modde, J Wittig, FM Heinemann, S Brundiers, ME Dämmrich…
Transplantation, 2013•journals.lww.comBackground Thrombotic microangiopathy (TMA) in renal transplants (rTx-TMA) is a serious
complication and is usually either recurrent TMA (RecTMA) due to humoral rejection (HR-
TMA) or due to calcineurin inhibitor toxicity (CNI-TMA). Although the triggers are known, our
knowledge about the thrombogenic transcriptome changes in the microvessels is
rudimentary. Methods We examined the expression of several prothrombotic and
antithrombotic genes in 25 biopsies with rTx-TMA (6 RecTMA, 9 HR-TMA, and 10 CNI-TMA) …
complication and is usually either recurrent TMA (RecTMA) due to humoral rejection (HR-
TMA) or due to calcineurin inhibitor toxicity (CNI-TMA). Although the triggers are known, our
knowledge about the thrombogenic transcriptome changes in the microvessels is
rudimentary. Methods We examined the expression of several prothrombotic and
antithrombotic genes in 25 biopsies with rTx-TMA (6 RecTMA, 9 HR-TMA, and 10 CNI-TMA) …
Background
Thrombotic microangiopathy (TMA) in renal transplants (rTx-TMA) is a serious complication and is usually either recurrent TMA (RecTMA) due to humoral rejection (HR-TMA) or due to calcineurin inhibitor toxicity (CNI-TMA). Although the triggers are known, our knowledge about the thrombogenic transcriptome changes in the microvessels is rudimentary.
Methods
We examined the expression of several prothrombotic and antithrombotic genes in 25 biopsies with rTx-TMA (6 RecTMA, 9 HR-TMA, and 10 CNI-TMA) and 8 controls. RNA from microdissected glomeruli of paraffin-embedded tissue was isolated and mRNA transcripts were quantified with real-time polymerase chain reaction after preamplification. Results were correlated with clinicopathologic parameters.
Results
Glomerular mRNA expression of KLF2, KLF4, and tPA was lower and that of PAI-1 was higher in rTx-TMA than in the controls. Glomerular mRNA expression of KLF2 and KLF4 correlated with that of tPA and inversely with that of PAI-1 in rTx-TMA. The mRNA expression of complement regulators CD46 and CD59 were higher in rTx-TMA than in the controls. Only in HR-TMA were glomerular ADAMTS13 and CD55 down-regulated.
Conclusions
The glomerular capillary bed seems to contribute to all subtypes of rTx-TMA by down-regulation of the endothelial transcription factors KLF2 and KLF4, indicating dedifferentiation with subsequent up-regulation of PAI-1 and down-regulation of tPA, resulting in inhibition of local fibrinolysis. Decreased glomerular expression of ADAMTS13 and CD55 could be an additional pathway toward microthrombosis exclusively in HR-TMA.
Lippincott Williams & Wilkins