Götherström Cecilia, Ringdén Olle, Tammik Charlotte, Zetterberg Eva, Westgren Magnus, Le Blanc Katarina
Division of Clinical Immunology, Karolinska Institutet, Huddinge University Hospital, Stockholm, Sweden.
Am J Obstet Gynecol. 2004 Jan;190(1):239-45. doi: 10.1016/j.ajog.2003.07.022.
Mesenchymal stem cells (MSCs) can be isolated from adult bone marrow and fetal liver. We investigated the immunologic properties of undifferentiated and differentiated human fetal MSCs.
Expression of HLA class I and II was investigated by flow cytometry and Western blot on undifferentiated fetal MSC and after in vitro differentiation to adipocytes and osteocytes. Alloreactivity was studied after adding fetal MSCs to allogeneic lymphocytes in mixed lymphocyte cultures.
Fetal MSCs expressed HLA class I but not HLA class II. The presence of interferon gamma (IFN-gamma) in the growth medium for 2 days initiated the intracellular synthesis of HLA class II, but 7 days of exposure was required for cell surface expression. Neither undifferentiated nor differentiated fetal MSCs induced proliferation of allogenic lymphocytes. Fetal MSCs treated with IFN-gamma suppressed alloreactive lymphocytes.
Undifferentiated and differentiated fetal MSCs do not elicit alloreactive lymphocyte proliferation. The results suggest that fetal MSCs have potentials for allogenic transplantation.
间充质干细胞(MSC)可从成人骨髓和胎儿肝脏中分离得到。我们研究了未分化和已分化的人胎儿MSC的免疫学特性。
通过流式细胞术和蛋白质印迹法,研究未分化胎儿MSC以及体外分化为脂肪细胞和骨细胞后的HLA I类和II类分子的表达。在混合淋巴细胞培养中,将胎儿MSC添加到同种异体淋巴细胞后,研究其同种异体反应性。
胎儿MSC表达HLA I类分子,但不表达HLA II类分子。生长培养基中存在干扰素γ(IFN-γ)2天可启动HLA II类分子的细胞内合成,但细胞表面表达需要暴露7天。未分化和已分化的胎儿MSC均未诱导同种异体淋巴细胞增殖。用IFN-γ处理的胎儿MSC可抑制同种异体反应性淋巴细胞。
未分化和已分化的胎儿MSC均不会引发同种异体反应性淋巴细胞增殖。结果表明胎儿MSC具有同种异体移植的潜力。