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Immature dendritic cells derived exosomes promotes immune tolerance by regulating T cell differentiation in renal transplantation.
Pang, Xin-Lu; Wang, Zhi-Gang; Liu, Lei; Feng, Yong-Hua; Wang, Jun-Xiang; Xie, Hong-Chang; Yang, Xian-Lei; Li, Jin-Feng; Feng, Gui-Wen.
Afiliación
  • Pang XL; Department of Kidney Transplantation, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.
  • Wang ZG; Department of Kidney Transplantation, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.
  • Liu L; Department of Kidney Transplantation, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.
  • Feng YH; Department of Kidney Transplantation, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.
  • Wang JX; Department of Kidney Transplantation, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.
  • Xie HC; Department of Kidney Transplantation, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.
  • Yang XL; Department of Kidney Transplantation, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.
  • Li JF; Department of Kidney Transplantation, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.
  • Feng GW; Department of Kidney Transplantation, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.
Aging (Albany NY) ; 11(20): 8911-8924, 2019 10 26.
Article en En | MEDLINE | ID: mdl-31655796
OBJECTIVE: To investigate the mechanism of immature dendritic cells-derived exosomes (imDECs) in the regulation of T cell differentiation and immune tolerance in renal allograft model mice. RESULTS: imDECs significantly improved the percent of survival, relieved inflammatory response, and reduced CD4+T cell infiltration. In addition, imDECs reduced the rejection associated cytokines in allograft mice, and increased the percentage of Foxp3+CD4+T cells in spleen and kidney tissues. imDECs suppressed the IL17+CD4+T cells and promoted the Foxp3+CD4+T cells under Th17 polarization condition. Moreover, miR-682 was found to be highly expressed in imDECs which suppressed the IL17+CD4+T cells and promoted the Foxp3+CD4+T cells. Luciferase reporter assay showed ROCK2 was a target of miR-682, and ROCK mRNA level was negative correlated with miR-682 mRNA level. CONCLUSION: miR-682 was highly expressed in imDECs, and imDECs-secreted miR-682 promoted Treg cell differentiation by negatively regulating ROCK2 to promote immune tolerance in renal allograft model mice. METHODS: Renal allograft model mice were established, and imDECs or mature dendritic cells-derived exosomes (mDECs) were injected into model mice. Rejection associated cytokines IFN-γ, IL-2, IL-17 levels in plasma were detected by ELISA. IL-17A, Foxp3, miR-682, ROCK2, p-STAT3, p-STAT5 expressions were measured by qRT-PCR or western blot.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Células Dendríticas / Linfocitos T CD4-Positivos / Diferenciación Celular / Trasplante de Riñón / Exosomas Límite: Animals Idioma: En Revista: Aging (Albany NY) Asunto de la revista: GERIATRIA Año: 2019 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Células Dendríticas / Linfocitos T CD4-Positivos / Diferenciación Celular / Trasplante de Riñón / Exosomas Límite: Animals Idioma: En Revista: Aging (Albany NY) Asunto de la revista: GERIATRIA Año: 2019 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos