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小鼠肾脏提取物对人脐带血中造血祖细胞增殖的影响。

Effect of murine kidney extracts on the proliferation of hematopoietic progenitor cells in human umbilical cord blood.

作者信息

Murakami M, Kashiwakura I, Hayase Y, Takahashi T A, Takagi Y

机构信息

Laboratory of Radiopharmaceutical Sciences, Hokkaido College of Pharmacy, Otaru, Japan.

出版信息

Biol Pharm Bull. 2000 Oct;23(10):1136-42. doi: 10.1248/bpb.23.1136.

Abstract

We examined the effect of murine kidney extract (MKE) on the clonal growth of highly purified CD34+ hematopoietic progenitor cells from human umbilical cord blood. MKE did not affect the total number of colonies of erythroid burst-forming units (BFU-E), granulocyte-macrophage colony-forming units (CFU-GM) or granulocyte-erythroid-macrophage-megakaryocyte colony-forming units (CFU-Mix/CFU-GEMM) in a methylcellulose culture with exogenous recombinant human granulocyte colony-stimulating factor, granulocytemacrophage colony-stimulating factor, interleukin-3, stem cell factor and erythropoietin. MKE significantly increased the proportion of BFU-E- or CFU-Mix-derived colonies, and suppressed the formation CFU-GM-derived colonies depending on the MKE dose. However, because of an increase in small megakaryocyte colonies derived from mature CFU-Meg MKE increased by approximately 40% the growth of megakaryocyte colony-forming units (CFU-Meg) in plasma clot culture stimulated by recombinant human thrombopoietin. Also MKE promoted an increase in hyperploid megakaryocytes, suggesting that the active factor(s) in MKE acts on the mature CFU-Meg and promotes the maturation of megakaryocytes. Gel-filtration high performance liquid chromatography of MKE showed that the promoting factor(s) in MKE was approximately 45 kDa. These results indicate that the factor(s) detected in MKE influence human hematopoiesis in vitro, especially thrombopoiesis.

摘要

我们研究了鼠肾提取物(MKE)对人脐带血中高度纯化的CD34 +造血祖细胞克隆生长的影响。在含有外源性重组人粒细胞集落刺激因子、粒细胞巨噬细胞集落刺激因子、白细胞介素-3、干细胞因子和促红细胞生成素的甲基纤维素培养体系中,MKE对红系爆式集落形成单位(BFU-E)、粒细胞巨噬细胞集落形成单位(CFU-GM)或粒细胞-红系-巨噬细胞-巨核细胞集落形成单位(CFU-Mix/CFU-GEMM)的集落总数没有影响。MKE可显著增加BFU-E或CFU-Mix来源的集落比例,并根据MKE剂量抑制CFU-GM来源的集落形成。然而,由于成熟CFU-Meg来源的小巨核细胞集落增加,MKE使重组人血小板生成素刺激的血浆凝块培养体系中巨核细胞集落形成单位(CFU-Meg)的生长增加了约40%。此外,MKE促进了超倍体巨核细胞的增加,表明MKE中的活性因子作用于成熟的CFU-Meg并促进巨核细胞的成熟。MKE的凝胶过滤高效液相色谱显示,MKE中的促进因子约为45 kDa。这些结果表明,在MKE中检测到的因子在体外影响人类造血,尤其是血小板生成。

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