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本文引用的文献

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Comparison of different hepatocyte cell lines for use in a hybrid artificial liver model.比较不同的肝细胞系在杂交人工肝模型中的应用。
Cytotechnology. 1997 May;24(1):39-45. doi: 10.1023/A:1007927906986.
2
Spatial development of the cultivation of a bone marrow stromal cell line in porous carriers.多孔载体中骨髓基质细胞系培养的空间发展。
Cytotechnology. 1999 Nov;31(3):225-31. doi: 10.1023/A:1008098313067.
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Cellular determinants affecting the rate of cytokine in cultures of human hematopoietic cells.
Biotechnol Bioeng. 1997 Apr 5;54(1):58-66. doi: 10.1002/(SICI)1097-0290(19970405)54:1<58::AID-BIT7>3.0.CO;2-X.
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The measurement of proliferation in tissue cultures by enumeration of cell nuclei.通过细胞核计数来测量组织培养中的细胞增殖。
J Natl Cancer Inst. 1951 Feb;11(4):773-95.
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Culture materials affect ex vivo expansion of hematopoietic progenitor cells.培养材料会影响造血祖细胞的体外扩增。
J Biomed Mater Res. 1997 Sep 5;36(3):347-59. doi: 10.1002/(sici)1097-4636(19970905)36:3<347::aid-jbm10>3.0.co;2-b.
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Evaluation of cytokines for expansion of the megakaryocyte and granulocyte lineages.用于巨核细胞和粒细胞谱系扩增的细胞因子评估。
Stem Cells. 1997;15(3):198-206. doi: 10.1002/stem.150198.
7
Ex vivo expansion of hematopoietic precursors, progenitors, and stem cells: the next generation of cellular therapeutics.造血前体细胞、祖细胞和干细胞的体外扩增:新一代细胞疗法。
Blood. 1996 Apr 15;87(8):3082-8.
8
Hematopoiesis on cellulose ester membranes. XIII. A combination of cloned stromal cells is needed to establish a hematopoietic microenvironment supportive of trilineal hematopoiesis.纤维素酯膜上的造血作用。十三、需要克隆基质细胞的组合来建立支持三系造血的造血微环境。
Exp Hematol. 1993 Feb;21(2):257-62.
9
Multilineal hematopoiesis in a three-dimensional murine long-term bone marrow culture.三维小鼠长期骨髓培养中的多系造血
Exp Hematol. 1995 Jan;23(1):26-32.
10
Human umbilical cord blood as a potential source of transplantable hematopoietic stem/progenitor cells.人脐带血作为可移植造血干/祖细胞的潜在来源。
Proc Natl Acad Sci U S A. 1989 May;86(10):3828-32. doi: 10.1073/pnas.86.10.3828.

采用多孔载体构建体外三维造血微环境用于小鼠骨髓细胞。

The construction of an in vitro three-dimensional hematopoietic microenvironment for mouse bone marrow cells employing porous carriers.

机构信息

International Center for Biotechnology, Osaka University, 2-1, Yamada-oka, Suita, Osaka, 565-0871, Japan.

出版信息

Cytotechnology. 2000 Oct;34(1-2):121-30. doi: 10.1023/A:1008157303025.

DOI:10.1023/A:1008157303025
PMID:19003386
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3449728/
Abstract

Spatial development of mouse bone marrow cellsemploying porous carriers was investigated in order todesign a bioreactor with a three-dimensionalhematopoietic microenvironment. Three types of porouscarriers were used for examining the spatialdevelopment of anchorage-dependent primary stromalcells as feeder cells. Stromal cells were found tospread well at a high density on a polyester nonwovendisc carrier (Fibra cel (FC)) under a scanningelectron microscope, while cells on porous cellulosebeads (Microcube (MC), 500 mum pore diameter)spread at a low density; cells on another type ofcellulose porous beads (CPB, 100 mum pore diameter)were globular. Mouse bone marrow cells wereinoculated to dishes containing three types of porouscarriers which shared more than 30% of the bottomsurface in a dish. The concentration of stromal cellsin the well containing FC was lower than that on theother two carriers. However, the weekly output oftotal hematopoietic cell (suspension cells) increasedbetween day 21 and 28 in the culture using FC while itdecreased monotonously in the cultures by use of theother two carriers. The proportion of progenitorcells (BFU-E, CFU-GM) in the total hematopoietic cellpopulation, after showing an initial decrease,increased after 1 week in the culture using FC whilethe proportion decreased monotonously to zero in thecultures using MC and CPB.

摘要

采用多孔载体研究了小鼠骨髓细胞的空间发育,以设计具有三维造血微环境的生物反应器。为了研究作为饲养细胞的锚定依赖性原代基质细胞的空间发育,使用了三种类型的多孔载体。在扫描电子显微镜下,发现基质细胞在聚酯无纺盘载体(Fibra cel(FC))上以高密度很好地扩散,而在多孔纤维素珠(Microcube(MC),500μm 孔径)上的细胞扩散密度较低;在另一种纤维素多孔珠(CPB,100μm 孔径)上的细胞呈球形。将小鼠骨髓细胞接种到含有三种多孔载体的培养皿中,这些载体在培养皿中共享超过 30%的底部表面。FC 孔中的基质细胞浓度低于其他两种载体。然而,在使用 FC 的培养中,悬浮细胞的总造血细胞(悬浮细胞)的每周产量在第 21 天至第 28 天之间增加,而在使用其他两种载体的培养中则单调下降。在使用 FC 的培养中,祖细胞(BFU-E、CFU-GM)在总造血细胞群体中的比例在最初下降后增加,而在 MC 和 CPB 的培养中则单调下降至零。