巨核细胞
克隆形成试验
川地34
祖细胞
血小板生成素
干细胞
移植
造血
血小板
免疫学
医学
流式细胞术
男科
生物
细胞生物学
内科学
细胞
遗传学
作者
Ru Feng,Chihiro Shimazaki,Tohru Inaba,Ryoichi Takahashi,Hideyo Hirai,Takehisa Kikuta,Toshiya Sumikuma,Noboru Yamagata,Eishi Ashihara,Naohisa Fujita,Masao Nakagawa
标识
DOI:10.1038/sj.bmt.1701273
摘要
Reliable markers for megakaryocytic reconstitution after peripheral blood stem cell transplantation (PBSCT) have not been established. To determine a convenient and reliable predictor, we measured the number of megakaryocyte progenitor cells in PBSC grafts by clonogenic and flow cytometric assays. Seventeen patients with hematological and solid malignancies were included in this study. For the clonogenic assay, we used thrombopoietin (TPO) as a growth factor to evaluate the maximum number of megakaryocyte progenitor cells. Using a flow cytometric assay, we examined the expression of platelet glycoproteins on CD34+ cells to count the number of megakaryocyte progenitor cells. We used buffer containing EDTA to prevent platelet adhesion to CD34+ cells and selected CD34+ cells by immunomagnetic beads. The best correlation was observed between the number of CD34+/CD41a+ cells and the time to platelet recovery (P = 0.0205), rather than the total number of CD34+ cells. In addition, a close correlation was observed between the number of CD34+/CD41a+ cells and colony-forming unit megakaryocyte (CFU-MK) (P = 0.0018). These observations suggest that the number of CD34+/CD41a+ cells is the best predictor for platelet reconstitution after PBSCT.
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