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小鼠胚胎和胎儿发育过程中的红系祖细胞和刺激因子。

Erythroid progenitor cells and stimulating factors during murine embryonic and fetal development.

作者信息

Johnson G R, Barker D C

出版信息

Exp Hematol. 1985 Mar;13(3):200-8.

PMID:3872223
Abstract

Murine embryonic and fetal yolk-sacs, peripheral blood, and livers were assayed for hemopoietic multipotential and progenitor cell content between days 6 and 13 of gestation. Multipotential cells (Mix-CFC), erythroid-committed progenitor cells (BFU-E), and nonerythroid progenitor cells (predominantly GM-CFC) were assayed by their ability to form hemopoietic colonies in vitro when stimulated by pokeweed-mitogen-stimulated spleen-cell-conditioned media (as a source of Multi-CSF) and either human or murine erythropoietin. Late erythroid progenitor cells (CFU-E) were stimulated to form colonies by erythropoietin. Mix-CFC, BFU-E, and nonerythroid cells were first detected on day 8 in yolk-sacs, day 9 in peripheral blood, and day 11 in liver. Maximum absolute numbers of yolk-sac Mix-CFC (182), BFU-E (331), and non-erythroid CFC (1358) occurred at 11 days of gestation. The maximum frequency of peripheral blood mix-CFC (24/10(5) cells) and BFU-E (55/10(5) cells) occurred at ten days of gestation. The absolute numbers of hepatic Mix-CFC, BFU-E, nonerythroid CFC, and CFU-E increased exponentially from 11 to 13 days' gestation. CFU-E were first detected at nine days in peripheral blood, at ten days in yolk-sac, and 11 days in liver and at all ages were equally responsive to erythropoietin. The maximum frequency (151/10(5) cells) of CFU-E in the peripheral blood and the maximum number per yolk-sac (1699) both occurred on day 11 of gestation. In confirmation of previous studies, yolk-sac fluid was found to contain a macrophage colony-stimulating activity. In addition, an activity capable of stimulating fetal liver CFU-E was also detected in yolk-sac fluid. However, no activity (Multi-CSF) capable of stimulating Mix-CFC or BFU-E was detected in either yolk-sac fluid or fetal plasma.

摘要

在妊娠第6至13天期间,对小鼠胚胎和胎儿的卵黄囊、外周血及肝脏进行了造血多能干细胞和祖细胞含量的检测。通过在体外受商陆丝裂原刺激的脾细胞条件培养基(作为多集落刺激因子的来源)以及人或小鼠促红细胞生成素刺激时形成造血集落的能力,来检测多能干细胞(混合集落形成细胞,Mix-CFC)、红系定向祖细胞(爆式红系集落形成单位,BFU-E)和非红系祖细胞(主要是粒-巨噬细胞集落形成单位,GM-CFC)。晚期红系祖细胞(红细胞集落形成单位,CFU-E)由促红细胞生成素刺激形成集落。Mix-CFC、BFU-E和非红系细胞最早分别于第8天在卵黄囊中、第9天在外周血中以及第11天在肝脏中被检测到。卵黄囊Mix-CFC(182个)、BFU-E(331个)和非红系CFC(1358个)的最大绝对数量出现在妊娠第11天。外周血混合集落形成细胞(24/10⁵细胞)和BFU-E(55/10⁵细胞)的最大频率出现在妊娠第10天。肝脏中Mix-CFC、BFU-E、非红系CFC和CFU-E的绝对数量从妊娠第11天到第13天呈指数增加。CFU-E最早于第9天在外周血中、第10天在卵黄囊中以及第11天在肝脏中被检测到,并且在所有年龄段对促红细胞生成素的反应均相同。外周血中CFU-E的最大频率(151/10⁵细胞)和每个卵黄囊的最大数量(1699个)均出现在妊娠第11天。正如之前研究所证实的,发现卵黄囊液中含有巨噬细胞集落刺激活性。此外,在卵黄囊液中还检测到一种能够刺激胎儿肝脏CFU-E的活性。然而,在卵黄囊液或胎儿血浆中均未检测到能够刺激Mix-CFC或BFU-E的活性(多集落刺激因子)。

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PLoS One. 2008 Apr 23;3(4):e2025. doi: 10.1371/journal.pone.0002025.
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Hematopoietic commitment during embryonic stem cell differentiation in culture.培养过程中胚胎干细胞分化期间的造血定向分化
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Human embryonic hemopoiesis. Kinetics of progenitors and precursors underlying the yolk sac----liver transition.
人类胚胎造血。卵黄囊向肝脏转变过程中祖细胞和前体细胞的动力学。
J Clin Invest. 1986 Jul;78(1):51-60. doi: 10.1172/JCI112572.
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Properties of the earliest clonogenic hemopoietic precursors to appear in the developing murine yolk sac.发育中小鼠卵黄囊中最早出现的克隆造血前体细胞的特性。
Proc Natl Acad Sci U S A. 1986 Jun;83(11):3851-4. doi: 10.1073/pnas.83.11.3851.
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A lethal myeloproliferative syndrome in mice transplanted with bone marrow cells infected with a retrovirus expressing granulocyte-macrophage colony stimulating factor.在移植了感染表达粒细胞-巨噬细胞集落刺激因子的逆转录病毒的骨髓细胞的小鼠中出现的致死性骨髓增殖综合征。
EMBO J. 1989 Feb;8(2):441-8. doi: 10.1002/j.1460-2075.1989.tb03396.x.