In-vitro generation of interleukin-10 secreting B-regulatory cells from donor adipose tissue derived mesenchymal stem cells and recipient peripheral blood mononuclear cells for potential cell therapy

被引:10
作者
Gupte, Kunal S. [1 ]
Vanikar, Aruna V. [1 ,2 ]
Trivedi, Hargovind L. [2 ,3 ]
Patel, Chetan N. [1 ,2 ]
Patel, Jignesh V. [1 ,2 ]
机构
[1] Dr HL Trivedi Inst Transplantat Sci ITS, GR Doshi & KM Mehta Inst Kidney Dis & Res Ctr IKD, Transplant Biol Res Lab, Dept Cell Therapy & Regenerat Med, Ahmadabad, Gujarat, India
[2] Dr HL Trivedi Inst Transplantat Sci ITS, GR Doshi & KM Mehta Inst Kidney Dis & Res Ctr IKD, Dept Pathol Lab Med Transfus Serv & Immunohematol, Civil Hosp Campus, Ahmadabad 380016, Gujarat, India
[3] Dr HL Trivedi Inst Transplantat Sci ITS, GR Doshi & KM Mehta Inst Kidney Dis & Res Ctr IKD, Dept Nephrol & Transplantat Med, Ahmadabad 380016, Gujarat, India
关键词
B-regulatory cells; Lipopolysaccharide E. coli; IL-10; Adipose tissue derived mesenchymal stem cells; Peripheral blood mononuclear cells; Immunomodulation; B10; CELLS; T-CELLS; IL-10; MICE; EXPRESSION; RECEPTORS; INDUCTION; SUBSET;
D O I
10.1016/j.bj.2017.01.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Interleukin-10 secreting B-cells are a major subset of B-regulatory cells (B-regs), commonly recognized as CD19(+)/38(hi)/24(hi)/IL10(+). They carry out immunomodulation by release of specific cytokines and/or cell-to-cell contact. We have generated B-regs in-vitro from donor adipose tissue derived mesenchymal stem cells (AD-MSC) and renal allograft recipient (RAR) peripheral blood mononuclear cells (PBMC) for potential cell therapy. Material and methods: Mononuclear cells separated by density gradient centrifugation from 50 ml anti-coagulated blood of 15-RAR and respective donors were analysed for baseline B-regs using appropriate antibodies. Equal amount (20 x 10(6) cells/ml) of stimulator (irradiated at 7.45 Gy/min for 10 min) and responder (non-irradiated) cells were co-cultured with in-vitro generated AD-MSC (1 x 10(6) cells/ml) in proliferation medium containing lipopolysaccharide from E. coli K12 strain at 37 degrees C with 5% CO2. Cells were harvested on day-7 and analyzed for viability, sterility, quantity, morphology and phenotyping. In-vitro generated B-reg levels were compared with baseline B-regs. Results: In-vitro generated B-reg count increased to 16.75% from baseline count of 3.35%. Conclusion: B-regs can be successfully generated in-vitro from donor AD-MSC and RAR PBMC for potential cell therapy.
引用
收藏
页码:49 / 54
页数:6
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