1. Impact of immunosuppressive agents on the expression of indoleamine 2,3-dioxygenase, heme oxygenase-1 and interleukin-7 in mesangial cells
- Author
-
Yong‑Xiang Zhuang, An‑Jian Chen, Zong‑Ping Chen, Ya‑Nan Guo, Ding‑Su Bao, Xin Wang, You‑Ping Li, Yuanliang Wang, Guang‑Heng Luo, Guo‑Biao Liang, and Yiping Lu
- Subjects
Cancer Research ,Cytochalasin B ,medicine.medical_treatment ,Glomerular Mesangial Cell ,mesangial cell ,Pharmacology ,Biology ,Biochemistry ,immunosuppressive agents ,Tacrolimus ,Cell Line ,Chronic allograft nephropathy ,Genetics ,medicine ,Humans ,Indoleamine-Pyrrole 2,3,-Dioxygenase ,RNA, Messenger ,Indoleamine 2,3-dioxygenase ,Molecular Biology ,Sirolimus ,interleukin-7 ,Interleukin ,heme oxygenase-1 ,in vitro ,Articles ,Mycophenolic Acid ,medicine.disease ,Glomerular Mesangium ,Heme oxygenase ,Real-time polymerase chain reaction ,Immunosuppressive drug ,3-dioxygenase ,Oncology ,Gene Expression Regulation ,Immunology ,Cyclosporine ,Molecular Medicine ,indoleamine 2 ,Signal Transduction - Abstract
Chronic allograft nephropathy (CAN) is a major cause of graft loss following kidney transplantation and may result from the interactions of various immune and non-immune factors. The aim of the present study was to establish an in vitro model of glomerular mesangial cell injury in order to examine the gene expression levels of indoleamine 2,3-dioxygenase (IDO), heme oxygenase-1 (HO-1) and interleukin-7 (IL-7) in mesangial cells during the healing process as well as to investigate the effects of various immunosuppressants on the expression of these genes. The HBZY-1 glomerular mesangial cell line was pre-treated in vitro with cytochalasin B for 2 h to induce reversible damage. Following the pre-treatment, the HBZY-1 cells were divided into five groups: Blank control group, cyclosporine A (CsA) group, tacrolimus (Tac) group, mycophenolate mofetil (MMF) group and rapamycin (RAPA) group. After treating the mesangial cells with each immunosuppressive drug for 6, 12 or 24 h, the mRNA and protein expression levels of IDO, HO-1 and IL-7 were examined using reverse transcription quantitative polymerase chain reaction (RT-qPCR), western blot and immunohistochemical analyses. The results showed that expression levels of HO-1 were significantly upregulated in response to treatment with CsA, FK506, RAPA and MMF, whereas the expression levels of IL-7 were markedly downregulated by treatment with the above immunosuppressants. CsA, FK506 and MMF significantly enhanced the expression levels of IDO, whereas RAPA exhibited no apparent effect on IDO. The present study may contribute to the understanding of the pathogenesis of CAN and provide novel strategies for the prevention and treatment of CAN.
- Published
- 2014