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低密度小鼠巨核细胞祖细胞(LD-CFU-M)的鉴定。

Identification of a light density murine megakaryocyte progenitor (LD-CFU-M).

作者信息

Chatelain C, De Bast M, Symann M

机构信息

Laboratory of Oncology and Experimental Hematology, Catholic University, Brussels, Belgium.

出版信息

Blood. 1988 Oct;72(4):1187-92.

PMID:3167202
Abstract

Murine bone marrow cells were separated on discontinuous Percoll gradients and assayed for their ability to give rise to megakaryocyte colonies. Ninety-one percent of the megakaryocyte progenitors (CFU-M) sedimented at densities between 1.070 and 1.080 g/mL. Six percent of CFU-M were found at densities between 1.060 and 1.070 g/mL, 2% between 1.050 and 1.060 g/mL, whereas less than 1% had a density either lower than 1.050 g/mL or higher than 1.080 g/mL. The number of doublings and endomitoses achieved by progenitors of density classes higher than 1.050 g/mL were similar. However, colonies derived from CFU-M of densities less than 1.050 g/mL (LD-CFU-M) had a higher probability of polyploidization and a lower probability of cell division in vitro. The inverse correlation found between the number of cells per colony and their DNA content was invariate regardless of the density class of the progenitors. The heterogeneity of the ploidy of cells within colonies increased continuously with increasing cell numbers per colony. The study if a short-period exposure of LD-CFU-M to acute thrombocytopenia could modify the ploidy of their progeny, mice were given rabbit antimouse platelet serum while control animals received normal rabbit serum. Twenty-four hours after injection, marrow was cultured. After a five-day culture period, no change in the number of colonies, doublings, ploidy, and heterogeneity of ploidy were observed between control and thrombocytopenic animals. The data suggests that LD-CFU-M are a distinct category of CFU-M, perhaps more mature than the common CFU-M.

摘要

将小鼠骨髓细胞在不连续的 Percoll 梯度上进行分离,并检测其产生巨核细胞集落的能力。91% 的巨核细胞祖细胞(CFU-M)沉降在密度为 1.070 至 1.080 g/mL 之间。6% 的 CFU-M 密度在 1.060 至 1.070 g/mL 之间,2% 在 1.050 至 1.060 g/mL 之间,而密度低于 1.050 g/mL 或高于 1.080 g/mL 的细胞不到 1%。密度高于 1.050 g/mL 的密度类别的祖细胞实现的倍增次数和核内有丝分裂次数相似。然而,密度低于 1.050 g/mL 的 CFU-M(低密度 CFU-M,LD-CFU-M)衍生的集落在体外多倍体化的概率较高,细胞分裂的概率较低。每个集落中的细胞数量与其 DNA 含量之间的负相关关系与祖细胞的密度类别无关。集落内细胞倍性的异质性随着每个集落细胞数量的增加而持续增加。为了研究短期暴露于急性血小板减少症的 LD-CFU-M 是否会改变其后代的倍性,给小鼠注射兔抗小鼠血小板血清,而对照动物接受正常兔血清。注射后 24 小时,培养骨髓。经过五天的培养期,在对照动物和血小板减少症动物之间未观察到集落数量、倍增次数、倍性和倍性异质性的变化。数据表明,LD-CFU-M 是 CFU-M 的一个独特类别,可能比普通的 CFU-M 更成熟。

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