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分化与未分化间充质干细胞的HLA表达及免疫学特性

HLA expression and immunologic properties of differentiated and undifferentiated mesenchymal stem cells.

作者信息

Le Blanc Katarina, Tammik Charlotte, Rosendahl Kerstin, Zetterberg Eva, Ringdén Olle

机构信息

Division of Clinical Immunology, Centre for Allogeneic Stem Cell Transplantation, Karolinska Institutet, Huddinge University Hospital, Stockholm, Sweden.

出版信息

Exp Hematol. 2003 Oct;31(10):890-6. doi: 10.1016/s0301-472x(03)00110-3.

Abstract

OBJECTIVE

Mesenchymal stem cells (MSC) do not elicit alloreactive lymphocyte responses due to immune modulations. We investigated the immunologic properties of MSC after differentiation along three lineages: bone, cartilage, and adipose.

METHODS AND RESULTS

Flow cytometry showed that undifferentiated MSC express HLA class I but not class II, although HLA class II was present intracellularly as detected by Western blot. Addition of interferon gamma (IFN-gamma) for 48 hours induced greater than 90% of cells to express HLA class II. No lymphocyte response was induced by allogeneic irradiated MSC as stimulators. Results were similar using MSC pretreated with IFN-gamma. After growth of cells in medium to induce differentiation to bone, cartilage, or adipose for 6 or 12 days, the expression of HLA class I increased but no class II was detected on the cell surface. The ability to upregulate HLA class II on the cell surface after exposure to IFN-gamma for 48 hours was clearly diminished after the cells had been cultured in differentiation medium for 6 or 12 days, with only 10% of cells expressing HLA class II. Using MSC grown in osteogenic, chondrogenic, or adipogenic medium as stimulator cells, no lymphocyte alloreactivity was seen, even if differentiated MSC had been pretreated with IFN-gamma. MSC inhibit mixed lymphocyte cultures, particularly after osteogenic differentiation. This suppression was further enhanced by IFN-gamma.

CONCLUSIONS

Undifferentiated and differentiated MSC do not elicit alloreactive lymphocyte proliferative responses and modulate immune responses. The findings support that MSC can be transplantable between HLA-incompatible individuals.

摘要

目的

间充质干细胞(MSC)由于免疫调节作用不会引发同种异体反应性淋巴细胞反应。我们研究了MSC沿骨、软骨和脂肪三个谱系分化后的免疫特性。

方法与结果

流式细胞术显示,未分化的MSC表达HLA I类分子但不表达II类分子,尽管蛋白质印迹法检测到细胞内存在HLA II类分子。添加干扰素γ(IFN-γ)48小时可诱导超过90%的细胞表达HLA II类分子。异体照射的MSC作为刺激剂未诱导淋巴细胞反应。使用经IFN-γ预处理的MSC,结果相似。在诱导向骨、软骨或脂肪分化的培养基中培养细胞6天或12天后,HLA I类分子的表达增加,但细胞表面未检测到II类分子。在分化培养基中培养6天或12天后,细胞在暴露于IFN-γ 48小时后上调细胞表面HLA II类分子的能力明显减弱,只有10%的细胞表达HLA II类分子。使用在成骨、成软骨或成脂肪培养基中生长的MSC作为刺激细胞,即使分化的MSC已用IFN-γ预处理,也未观察到淋巴细胞同种异体反应性。MSC抑制混合淋巴细胞培养,尤其是在成骨分化后。IFN-γ进一步增强了这种抑制作用。

结论

未分化和分化的MSC均不会引发同种异体反应性淋巴细胞增殖反应并调节免疫反应。这些发现支持MSC可在HLA不相容的个体之间进行移植。

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