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连续骨髓培养中造血微环境的起源。

The origin of the hematopoietic microenvironment in continuous bone marrow culture.

作者信息

Bentley S A, Knutsen T, Whang-Peng J

出版信息

Exp Hematol. 1982 Apr;10(4):367-72.

PMID:7047183
Abstract

Marrow-derived adherent cells (MDAC) have been shown to provide a microenvironment which supports the proliferation of hematopoietic stem cells in continuous bone marrow culture. A study was undertaken to investigate the origin of MDAC. Normal CBA mice were transplanted with marrow cells from CBA donors bearing two T6 chromosomes. Five weeks after transplantation, the mice were sacrificed, their marrow cells explanted in liquid culture and the numbers of T6 positive and T6 negative mitoses were monitored during cultivation of MDAC. After 6 weeks, established MDAC monolayers were recharged with second explants of marrow cells and their capacity to support HSC proliferation in continuous marrow culture was assessed. The number of T6 positive mitoses declined steadily during the period of MDAC cultivation and none were detected after 4 weeks. The MDAC monolayers were able to support in vitro proliferation of CFUs for periods of at least 5 weeks. These results suggest that the in vitro hematopoietic microenvironment was of recipient origin and therefore stromal.

摘要

骨髓来源的贴壁细胞(MDAC)已被证明能提供一种微环境,在连续骨髓培养中支持造血干细胞的增殖。开展了一项研究以调查MDAC的起源。将带有两条T6染色体的CBA供体的骨髓细胞移植到正常CBA小鼠体内。移植后五周,处死小鼠,取出其骨髓细胞进行液体培养,并在MDAC培养过程中监测T6阳性和T6阴性有丝分裂的数量。六周后,用骨髓细胞的第二次外植体对已建立的MDAC单层进行再接种,并评估其在连续骨髓培养中支持造血干细胞增殖的能力。在MDAC培养期间,T6阳性有丝分裂的数量稳步下降,4周后未检测到。MDAC单层能够在至少5周的时间内支持集落形成单位的体外增殖。这些结果表明,体外造血微环境起源于受体,因此是基质性的。

相似文献

1
The origin of the hematopoietic microenvironment in continuous bone marrow culture.连续骨髓培养中造血微环境的起源。
Exp Hematol. 1982 Apr;10(4):367-72.
2
Close range cell:cell interaction required for stem cell maintenance in continuous bone marrow culture.近距离细胞:细胞相互作用是连续骨髓培养中干细胞维持所必需的。
Exp Hematol. 1981 Mar;9(3):308-12.
3
In vitro analysis of the contributions of adherent cell layer and recharging population to hemopoietic cell proliferation in long-term bone marrow cultures.长期骨髓培养中贴壁细胞层和再增殖群体对造血细胞增殖贡献的体外分析。
Exp Hematol. 1981 Apr;9(4):319-25.
4
Potentials for lymphoid differentiation by cells from long term cultures of bone marrow.来自骨髓长期培养的细胞进行淋巴样分化的潜能。
Exp Hematol. 1980 Jan;8(1):65-76.
5
Increased survival of CBA pluripotent haemopoietic stem cells in vitro induced by a marrow stromal factor in Sl/Sld mice.骨髓基质因子诱导Sl/Sld小鼠体内CBA多能造血干细胞在体外存活率增加。
Exp Hematol. 1979 Jul;7(6):324-7.
6
Cryopreservation of marrow and stromal progenitor cells: use of long-term liquid culture as a measure of the recovery of renewable hematopoietic and stromal cells.骨髓和基质祖细胞的冷冻保存:采用长期液体培养作为可再生造血细胞和基质细胞恢复情况的一种衡量方法。
Exp Hematol. 1983 Apr;11(4):315-23.
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Biology of marrow stromal cell lines derived from long-term bone marrow cultures of Trp53-deficient mice.源自Trp53基因缺陷小鼠长期骨髓培养的骨髓基质细胞系生物学特性
Radiat Res. 1999 Jul;152(1):29-40.
8
Hemopoietic stromal precursors in long-term culture of bone marrow: I. Precursor characteristics, kinetics in culture, and dependence on quality of donor hemopoietic cells in chimeras.骨髓长期培养中的造血基质前体细胞:I. 前体细胞特征、培养动力学以及对嵌合体中供体造血细胞质量的依赖性。
Exp Hematol. 1983 Mar;11(3):231-42.
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[Transplantation of mesenchymal derived stem cells followed by G-CSF injection can reconstitute hematopoiesis of lethally irradiated BALB/c mice].间充质来源干细胞移植后注射粒细胞集落刺激因子可重建经致死剂量照射的BALB/c小鼠的造血功能
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2002 Feb;24(1):20-4.
10
The membrane-bound isoform of stem cell factor synergizes with soluble flt3 ligand in supporting early hematopoietic cells in long-term cultures of normal and aplastic anemia bone marrow.干细胞因子的膜结合异构体与可溶性fms样酪氨酸激酶3配体协同作用,在正常和再生障碍性贫血骨髓的长期培养中支持早期造血细胞。
Exp Hematol. 1998 May;26(5):365-73.

引用本文的文献

1
Preliminary high-dose irradiation of the recipient and associated damage of bone marrow stromal compartment enables bone marrow stroma transplantation.对受体进行初步大剂量照射以及骨髓基质区室的相关损伤可实现骨髓基质移植。
Sci Rep. 2025 Jul 1;15(1):22295. doi: 10.1038/s41598-025-07709-9.
2
CFU-F circulating in cord blood.脐血中循环的集落形成单位-成纤维细胞(CFU-F)
Blut. 1987 Jun;54(6):351-9. doi: 10.1007/BF00626017.
3
Hematopoietic microenvironment. Origin, lineage, and transplantability of the stromal cells in long-term bone marrow cultures from chimeric mice.
造血微环境。嵌合小鼠长期骨髓培养中基质细胞的起源、谱系及移植能力。
J Clin Invest. 1988 Apr;81(4):1072-80. doi: 10.1172/JCI113419.
4
Usefulness of Y-body study on bone marrow smears to demonstrate the origin of fibroblast stromal cells in allogeneic bone marrow transplantation.
Blut. 1990 Jul;61(1):14-6. doi: 10.1007/BF01739427.
5
Origin of marrow stromal cells and haemopoietic chimaerism following bone marrow transplantation determined by in situ hybridisation.通过原位杂交确定骨髓移植后骨髓基质细胞的起源和造血嵌合体。
Br J Cancer. 1990 Mar;61(3):385-9. doi: 10.1038/bjc.1990.84.