[SIRT1 deficiency in CD4+T cells induces acute graft-versus-host disease after allogeneic hematopoietic stem cell transplantation]

Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2018 Jul 28;43(7):697-703. doi: 10.11817/j.issn.1672-7347.2018.07.001.
[Article in Chinese]

Abstract

To study the relationship between acute graft-versus-host disease (aGVHD) and the SIRT1 expression in peripheral blood CD4+T cells from patients after allogeneic hematopoietic stem cell transplantation (allo-HSCT). Methods: We collected 40 patients who underwent allo-HSCT from human leukocyte antigen (HLA)-identical sibling donors. SIRT1 expression level in CD4+T cells was measured by real-time PCR and Western blot. Acetylation and phosphorylation of STAT3 in CD4+T cells were detected by Western blot. The binding level between SIRT1 and STAT3 in CD4+T cells was analyzed by co-immunoprecipitation and Western blot. Over-expression of SIRT1 in aGVHD CD4+T cells, as well as STAT3 acetylation and phosphorylation were measured by Western blot. The mRNA levels of RORγt, IL-17A, IL-17F related to Th17 were detected by real-time PCR. Results: SIRT1 expression was significantly down-regulated, while STAT3 expression, acetylation and phosphorylation levels were significantly up-regulated in patients with aGVHD compared with patients without aGVHD. The STAT3 acetylation was positively correlated with STAT3 phosphorylation (r=0.69, P<0.01). Less SIRT1-STAT3 complexes were found in CD4+T cells from patients with aGVHD compared with patients without aGVHD. After SIRT1 over-expression in aGVHD CD4+T cells, the STAT3 acetylation and phosphorylation, and the expression of RORγt, IL-17A, and IL-17F related to Th17 were significantly down-regulated (P<0.05). Conclusion: SIRT1 deficiency in CD4+T cells plays a crucial role in up-regulation of STAT3 acetylation and phosphorylation, the increase of Th17 related gene expression, and induction of aGVHD after allogeneic hematopoietic stem cell transplantation.

目的:研究异基因造血干细胞移植患者外周血CD4+T细胞中SIRT1基因表达水平与急性移植物抗宿主病(acute graft-versus-host disease,aGVHD)的关系。方法:收集40例行同胞全相合异基因造血干细胞移植患者的血液样本,采用实时定量PCR和Western印迹检测各组患者SIRT1的表达水平;采用Western印迹检测各组患者STAT3乙酰化及磷酸化水平;采用免疫共沉淀和Western印迹检测各组患者SIRT1和STAT3结合水平;aGVHD患者CD4+T细胞过表达SIRT1后采用Western印迹检测STAT3乙酰化及磷酸化水平,采用实时定量PCR检测Th17相关基因RORγt,IL-17A,IL-17F的表达。结果:与未发生aGVHD患者比较,aGVHD患者外周血CD4+T细胞中SIRT1表达水平明显降低;STAT3表达水平、乙酰化及磷酸化水平均明显升高,且STAT3乙酰化与磷酸化水平呈明显正相关(r=0.69,P<0.01);STAT3与SIRT1结合显著减少。aGVHD患者外周血CD4+T细胞中过表达SIRT1后,STAT3乙酰化及磷酸化水平均明显降低,RORγt,IL-17A,IL-17F的表达明显减少(P<0.05)。结论:CD4+T细胞中SIRT1表达不足是异基因造血干细胞移植术后患者STAT3高度乙酰化及磷酸化,介导Th17的相关基因表达升高,进而诱发aGVHD的重要因素。.

MeSH terms

  • Acute Disease
  • CD4-Positive T-Lymphocytes / metabolism*
  • Down-Regulation
  • Graft vs Host Disease / etiology*
  • Graft vs Host Disease / metabolism
  • Hematopoietic Stem Cell Transplantation*
  • Histocompatibility Antigens Class I
  • Humans
  • Interleukin-17 / metabolism
  • Nuclear Receptor Subfamily 1, Group F, Member 3 / metabolism
  • STAT3 Transcription Factor / metabolism*
  • Sirtuin 1 / deficiency*
  • Sirtuin 1 / metabolism
  • Transplantation, Homologous
  • Up-Regulation

Substances

  • Histocompatibility Antigens Class I
  • IL17A protein, human
  • Interleukin-17
  • Nuclear Receptor Subfamily 1, Group F, Member 3
  • RORC protein, human
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • histocompatibility antigen DLA
  • SIRT1 protein, human
  • Sirtuin 1