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基质依赖培养中一种新型双能髓系祖细胞克隆的自我更新与分化

Self-renewal and differentiation of a novel bipotent myeloid progenitor clone in the stroma-dependent culture.

作者信息

Okubo T, Yanai N, Obinata M

机构信息

Department of Cell Biology, Institute of Development, Aging and Cancer, Tohoku University, Sendai, Japan.

出版信息

Exp Hematol. 2000 Jun;28(6):651-9. doi: 10.1016/s0301-472x(00)00166-1.

Abstract

To understand regulation of myeloid development, it is necessary to obtain the myeloid progenitor cell lines with self-renewal and differentiation capacities. Because prolonged hematopoiesis occurs with the production of myeloid cells at all stages of differentiation in the Dexter-type long-term bone marrow cultures, we tried to obtain stroma-dependent myeloid progenitor cells starting from the long-term bone marrow culture. Murine cobblestone areas generated in long-term bone marrow cultures were serially passaged every 10 days. After 4 months, the resultant hematopoietic cells, designated as DFC, were passaged on a monolayer of established spleen stromal cell line, MSS62. After 10-12 passages of DFC cells on MSS62, several clones were obtained by colony formation on MSS62 cell layer. Among these clones, DFC-a cells could be maintained for a long period by coculturing with the established stromal cell line, MSS62.DFC-a cells proliferated by forming cobblestones and contained blast cells, granulocytes, and macrophages. Cell sorting and coculture experiments indicated that the blast type cells exhibiting c-Kit(+) Gr-1(-) Mac-1(-), stroma-dependently self-renewed, and spontaneously differentiated toward granulocytes (c-Kit(+) Gr-1(+) Mac-1(+)) and macrophages (c-Kit(low/+) Gr-1(-) Mac-1(high)). Although most of DFC-a cells expressed c-Kit, SCF-c-Kit interaction was not always necessary for their growth. In the presence of stromal cells, growth and differentiation of DFC-a cells were stimulated by GM-CSF or IL-3. Without stromal cells, DFC-a was transiently expanded by GM-CSF or IL-3 but could not be maintained constantly by these cytokines. The present study demonstrated that DFC-a is a novel bipotent myeloid progenitor cell clone as a simple model system of stroma-dependent myeloid development. It may reflect distinct properties for the earliest myeloid progenitor cells in vivo. It is of interest to know what signals are provided by MSS62 stromal cells to maintain the myeloid progenitor cells.

摘要

为了解髓系发育的调控机制,有必要获得具有自我更新和分化能力的髓系祖细胞系。由于在德克斯特型长期骨髓培养中,随着髓系细胞在分化的各个阶段产生,会出现长时间的造血过程,我们试图从长期骨髓培养物中获得依赖基质的髓系祖细胞。长期骨髓培养中产生的小鼠鹅卵石区域每10天进行一次连续传代。4个月后,将所得的造血细胞命名为DFC,接种到已建立的脾脏基质细胞系MSS62的单层细胞上。DFC细胞在MSS62上经过10 - 12代传代后,通过在MSS62细胞层上形成集落获得了几个克隆。在这些克隆中,DFC - a细胞通过与已建立的基质细胞系MSS62共培养可长期维持。DFC - a细胞通过形成鹅卵石样结构进行增殖,并包含原始细胞、粒细胞和巨噬细胞。细胞分选和共培养实验表明,表现为c - Kit(+) Gr - 1(-) Mac - 1(-)的原始型细胞依赖基质进行自我更新,并自发分化为粒细胞(c - Kit(+) Gr - 1(+) Mac - 1(+))和巨噬细胞(c - Kit(low/+) Gr - 1(-) Mac - 1(high))。尽管大多数DFC - a细胞表达c - Kit,但SCF - c - Kit相互作用并非其生长所必需。在有基质细胞存在的情况下,GM - CSF或IL - 3可刺激DFC - a细胞生长和分化。没有基质细胞时,GM - CSF或IL - 3可使DFC - a短暂扩增,但这些细胞因子无法使其持续维持。本研究表明,DFC - a是一种新型的双能髓系祖细胞克隆,可作为依赖基质的髓系发育的简单模型系统。它可能反映了体内最早的髓系祖细胞的独特特性。了解MSS62基质细胞提供了哪些信号来维持髓系祖细胞是很有意义的。

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