Journal article

Pivotal Advance: Up-regulation of acetylcholine synthesis and paracrine cholinergic signaling in intravascular transplant leukocytes during rejection of rat renal allografts


Authors listHecker, Andreas; Mikulski, Zbigniew; Lips, Katrin S.; Pfeil, Uwe; Zakrzewicz, Anna; Wilker, Sigrid; Hartmann, Petra; Padberg, Winfried; Wessler, Ignaz; Kummer, Wolfgang; Grau, Veronika

Publication year2009

Pages13-22

JournalJournal of Leukocyte Biology

Volume number86

Issue number1

ISSN0741-5400

eISSN1938-3673

Open access statusBronze

DOI Linkhttps://doi.org/10.1189/JLB.1107722

PublisherOxford University Press


Abstract
During acute rejection, large numbers of leukocytes accumulate in the blood vessels of experimental renal allografts. About 70% of them are activated, cytotoxic monocytes that appear to be involved in allograft destruction. ACh exerts anti-inflammatory effects upon monocytes/macrophages and has been proposed to be a key player in neuroimmunological interactions. Its short half-life, however, makes it unlikely that neuronal ACh affects blood leukocytes. Renal transplantation was performed in the allogeneic DA to LEW and in the isogeneic LEW to LEW rat strain combination. Intravascular leukocytes were harvested after 4 days, and the expression of CHT1, cChAT, pChAT, and nAChR subunits was investigated by RT-PCR, immunoblotting, and immunohistochemistry. Monocytes were identified by double-labeling with ED1-antibody, directed to a CD68-like antigen. ACh content was measured by HPLC. [Ca2+](i) was monitored by Fura-2. Intravascular graft leukocytes express CHT1 and cChAT mRNA and protein and pChAT protein. Their expression is strongly up-regulated in vivo during acute allograft rejection. Immunohistochemistry revealed CHT1, cChAT, and pChAT protein in ED1-positive monocytes. The ACh content of allograft intravascular leukocytes was sixfold higher than that of isografts. Intravascular leukocytes express nAChR subunits, and an ATP-induced increase in [Ca2+](i) was augmented in vitro by a nAChR inhibitor in allograft but not isograft leukocytes. Intravascular graft leukocytes, among them monocytes, up-regulate non-neuronal ACh synthesis and develop auto-/paracrine cholinergic attenuation of ATP signaling during acute allograft rejection. J. Leukoc. Biol. 86: 13-22; 2009.



Citation Styles

Harvard Citation styleHecker, A., Mikulski, Z., Lips, K., Pfeil, U., Zakrzewicz, A., Wilker, S., et al. (2009) Pivotal Advance: Up-regulation of acetylcholine synthesis and paracrine cholinergic signaling in intravascular transplant leukocytes during rejection of rat renal allografts, Journal of Leukocyte Biology, 86(1), pp. 13-22. https://doi.org/10.1189/JLB.1107722

APA Citation styleHecker, A., Mikulski, Z., Lips, K., Pfeil, U., Zakrzewicz, A., Wilker, S., Hartmann, P., Padberg, W., Wessler, I., Kummer, W., & Grau, V. (2009). Pivotal Advance: Up-regulation of acetylcholine synthesis and paracrine cholinergic signaling in intravascular transplant leukocytes during rejection of rat renal allografts. Journal of Leukocyte Biology. 86(1), 13-22. https://doi.org/10.1189/JLB.1107722



Keywords


ACETYLTRANSFERASE MESSENGER-RNAADULT-RATALTERNATIVE SPLICE VARIANTDORSAL-ROOT GANGLIONHUMAN MONOCYTESKidney transplantationLYMPHOID ORGANSMONONUCLEAR LEUKOCYTESNONNEURONAL ACETYLCHOLINERECEPTOR SUBTYPEST-Lymphocytes

Last updated on 2025-18-06 at 13:48