Vanikar A V, Mishra V V, Firoz A, Shah V R, Dave S D, Patel R D, Kanodia K V, Patel J V, Patel C N, Trivedi H L
Department of Pathology, Laboratory Medicine, Transfusion Services and Immunohematology, Institute of Kidney Diseases and Transplantation Sciences, Gulabben Rasiklal Doshi and Kamlaben Mafatlal Mehta Institute, Ahmedabad, Gujarat, India.
Transplant Proc. 2007 Apr;39(3):658-61. doi: 10.1016/j.transproceed.2007.01.048.
We report the generation of 30 healthy human embryonic stem cell (h-ESC) lines from 33 voluntary oocyte donors using a donor somatic cell nuclear transfer (SCNT) technique on 190 oocytes. Our aim was to coculture them with their own bone marrow (BM) to generate hematopoietic progenitor cells for therapeutic purposes. Pluripotency and undifferentiated stage were confirmed using molecular cell surface markers. Normal karyotype of these cell lines was confirmed. Here we demonstrate that SCNT-h-ESCs differentiate to hematopoietic precursors when cocultured with unmodified, nonirradiated donor BM. We did not use any xenogeneic material for this hematopoietic differentiation. Hematopoietic precursors derived from them expressed cell surface antigens CD45/34. When further cultured with hematopoietic growth factors these hematopoietic precursors formed characteristic myeloid, erythroid, and megakaryocyte lineages. Phenotypic CD34+ cells derived from NT-h-ESCs were functionally similar to their counterparts in primary hematopoietic tissues like BM, umbilical cord, and blood. More terminally differentiated hematopoietic cells derived from h-ESCs under these culture conditions also expressed normal surface antigens like glycophorin A on erythroid cells, CD15 on myeloid cells, and CD41 on megakaryocytes. We report generation of hematopoietic progenitor cells from h-ESC lines by a SCNT technique, with differentiation into further lineages with structural and functional similarities to their adult counterparts in vivo. This novel alternative source of CD34+ stem cells from h-ESC lines generated without any xenogeneic material might be used to create transplantation tolerance, to implement regenerative medicine, and to treat autoimmune disorders.
我们报告了使用供体体细胞核移植(SCNT)技术,从33名自愿捐赠卵母细胞的供体中获取了30条健康的人类胚胎干细胞(h-ESC)系,共使用了190枚卵母细胞。我们的目的是将它们与自身骨髓(BM)共培养,以生成用于治疗目的的造血祖细胞。使用分子细胞表面标志物确认了多能性和未分化阶段。确认了这些细胞系的正常核型。在这里,我们证明,当与未修饰、未辐照的供体BM共培养时,SCNT-h-ESCs可分化为造血前体细胞。我们在这种造血分化过程中未使用任何异种材料。源自它们的造血前体细胞表达细胞表面抗原CD45/34。当与造血生长因子进一步培养时,这些造血前体细胞形成了特征性的髓系、红系和巨核细胞系。源自NT-h-ESCs的表型CD34+细胞在功能上与其在原发性造血组织(如BM、脐带和血液)中的对应细胞相似。在这些培养条件下,源自h-ESCs的更多终末分化造血细胞也表达正常表面抗原,如红系细胞上的血型糖蛋白A、髓系细胞上的CD15和巨核细胞上的CD41。我们报告了通过SCNT技术从h-ESC系生成造血祖细胞,并分化为进一步的细胞系,其结构和功能与体内成年对应细胞相似。这种无需任何异种材料生成的h-ESC系的新型CD34+干细胞替代来源,可能用于建立移植耐受性、实施再生医学以及治疗自身免疫性疾病。