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支持小鼠造血母细胞分化为破骨细胞样细胞的基质细胞系的建立与鉴定。

Establishment and characterization of stromal cell lines that support differentiation of murine hematopoietic blast cells into osteoclast-like cells.

作者信息

Takanashi H, Matsuishi T, Yoshizato K

机构信息

Development Biology Laboratory, Faculty of Science, Hiroshima University, Japan.

出版信息

In Vitro Cell Dev Biol Anim. 1994 Jun;30A(6):384-93. doi: 10.1007/BF02634359.

Abstract

This study aimed to establish and characterize a new stromal cell line that supports the proliferation of hematopoietic blast cells and their differentiation into osteoclast-like cells. Cells isolated from the calvaria of neonatal Balb/c mice were subcultured every 2 to 4 days at 1.2 x 10(4) cells/cm2. After 18 passages the cells had become immortalized and were designated as MCHT-1. MCHT-1 cells were found to support the proliferation of hematopoietic blast cells and their differentiation into osteoclast-like cells when these two cells were co-cultured in the presence of 1 alpha,25(OH)2D3 and dexamethasone. However, because the MCHT-1 cells showed heterogeneity, cloning was performed and each clone was characterized. All the clones obtained supported the proliferation of hematopoietic blast cells and their differentiation into osteoclast-like cells irrespective of their obvious differences in growth capacities and cytochemical characteristics. However, the time-course of the appearance of osteoclast-like cells differed among clones. The supportive effect of these clonal stromal cells on differentiation of hematopoietic blast cells into osteoclast-like cells was completely dependent on the presence of 1 alpha,25(OH)2D3 and dexamethasone. These clonal MCHT-1 cells are expected to be useful for precise analysis of the proliferation and differentiation of osteoclasts.

摘要

本研究旨在建立并鉴定一种新的基质细胞系,该细胞系可支持造血母细胞的增殖及其向破骨细胞样细胞的分化。从新生Balb/c小鼠颅骨分离的细胞,以1.2×10⁴个细胞/cm²的密度每2至4天进行一次传代培养。传代18次后,细胞实现永生化,并命名为MCHT-1。当这两种细胞在1α,25(OH)₂D₃和地塞米松存在的情况下共培养时,发现MCHT-1细胞可支持造血母细胞的增殖及其向破骨细胞样细胞的分化。然而,由于MCHT-1细胞表现出异质性,因此进行了克隆并对每个克隆进行了鉴定。获得的所有克隆均支持造血母细胞的增殖及其向破骨细胞样细胞的分化,无论它们在生长能力和细胞化学特征上存在明显差异。然而,破骨细胞样细胞出现的时间进程在各克隆之间有所不同。这些克隆基质细胞对造血母细胞向破骨细胞样细胞分化的支持作用完全依赖于1α,25(OH)₂D₃和地塞米松的存在。这些克隆的MCHT-1细胞有望用于精确分析破骨细胞的增殖和分化。

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