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血小板生成素(TPO)/Mpl系统的作用:c-Mpl样分子/TPO信号增强非洲爪蟾的早期造血作用。

Role of the thrombopoietin (TPO)/Mpl system: c-Mpl-like molecule/TPO signaling enhances early hematopoiesis in Xenopus laevis.

作者信息

Kakeda Minoru, Kyuno Jun-ichi, Kato Takashi, Nishikawa Mitsuo, Asashima Makoto

机构信息

Department of Biological Science, Graduate School of Science, University of Tokyo, Tokyo 153-8902, Japan.

出版信息

Dev Growth Differ. 2002 Feb;44(1):63-75. doi: 10.1046/j.1440-169x.2002.00622.x.

DOI:10.1046/j.1440-169x.2002.00622.x
PMID:11869293
Abstract

Multiple organs are induced in the primitive embryonic ectoderm excised from blastula stage Xenopus laevis embryos, under the strict control of mesoderm inducing factors. This in vitro system is useful for exploring the mechanisms of development. In this study, the function of thrombopoietin (TPO)/c-Mpl signaling in the development of hematopoietic cells was investigated. An optimal hematopoietic cell induction system was established to evaluate the influence of growth factors on hematopoiesis. It was found that exogenous TPO enhanced hematopoiesis in explants induced by activin and bone morphogenetic protein (BMP)-4 and increased the number of both erythrocytes and leukocytes in a dose-dependent manner. Addition of anti-c-Mpl antibody completely inhibited the expansion of hematopoietic cells stimulated by TPO, and the antibody specifically recognized blood-like cells. These results demonstrate that TPO acts on hematopoietic progenitors induced in explants and the c-Mpl-like molecule in Xenopus mediates the cellular function of TPO. We also found that forced expression of TPO in embryos promoted hematopoiesis in the ventral blood island and the dorsal-- lateral plate mesoderm. These results suggest that hematopoietic stem and progenitor cells are regulated by TPO/c-Mpl signaling from when they appear in their ontogeny. They also suggest that TPO/c-Mpl signaling play a crucial role in the formation of hematopoietic cells in Xenopus.

摘要

在中胚层诱导因子的严格控制下,从囊胚期非洲爪蟾胚胎中切除的原始胚胎外胚层可诱导形成多个器官。这个体外系统有助于探索发育机制。在本研究中,研究了血小板生成素(TPO)/c-Mpl信号在造血细胞发育中的作用。建立了一个优化的造血细胞诱导系统来评估生长因子对造血的影响。发现外源性TPO增强了激活素和骨形态发生蛋白(BMP)-4诱导的外植体中的造血作用,并以剂量依赖的方式增加了红细胞和白细胞的数量。添加抗c-Mpl抗体完全抑制了TPO刺激的造血细胞的扩增,并且该抗体特异性识别类血细胞。这些结果表明,TPO作用于外植体中诱导的造血祖细胞,非洲爪蟾中的c-Mpl样分子介导了TPO的细胞功能。我们还发现,胚胎中TPO的强制表达促进了腹侧血岛和背外侧板中胚层的造血作用。这些结果表明,造血干细胞和祖细胞从个体发生中出现时就受到TPO/c-Mpl信号的调节。它们还表明,TPO/c-Mpl信号在非洲爪蟾造血细胞的形成中起关键作用。

相似文献

1
Role of the thrombopoietin (TPO)/Mpl system: c-Mpl-like molecule/TPO signaling enhances early hematopoiesis in Xenopus laevis.血小板生成素(TPO)/Mpl系统的作用:c-Mpl样分子/TPO信号增强非洲爪蟾的早期造血作用。
Dev Growth Differ. 2002 Feb;44(1):63-75. doi: 10.1046/j.1440-169x.2002.00622.x.
2
Role for C-MPL and its ligand thrombopoietin in early hematopoiesis.C-MPL及其配体血小板生成素在早期造血中的作用。
Leuk Lymphoma. 1997 Dec;28(1-2):51-6. doi: 10.3109/10428199709058330.
3
Role of c-mpl in early hematopoiesis.c-mpl在早期造血过程中的作用。
Blood. 1998 Jul 1;92(1):4-10.
4
Hematopoietic deficiencies in c-mpl and TPO knockout mice.c-mpl和血小板生成素基因敲除小鼠的造血缺陷
Stem Cells. 1998;16(1):1-6. doi: 10.1002/stem.160001.
5
A role for thrombopoietin in hemangioblast development.血小板生成素在成血管细胞发育中的作用。
Stem Cells. 2003;21(3):272-80. doi: 10.1634/stemcells.21-3-272.
6
Thrombopoietin: expression of its receptor MPL and proliferative effects on leukemic cells.血小板生成素:其受体MPL的表达及对白血病细胞的增殖作用。
Leukemia. 1996 Sep;10(9):1405-21.
7
Recombinant human c-Mpl ligand (thrombopoietin) not only acts on megakaryocyte progenitors, but also on erythroid and multipotential progenitors in vitro.重组人c-Mpl配体(血小板生成素)不仅在体外作用于巨核细胞祖细胞,还作用于红系祖细胞和多能祖细胞。
Exp Hematol. 1997 Sep;25(10):1025-33.
8
Hematopoietic stem cell deficiencies in mice lacking c-Mpl, the receptor for thrombopoietin.缺乏血小板生成素受体c-Mpl的小鼠中的造血干细胞缺陷。
Proc Natl Acad Sci U S A. 1998 Feb 3;95(3):1195-200. doi: 10.1073/pnas.95.3.1195.
9
Thrombopoietin and its receptor.血小板生成素及其受体。
Eur Cytokine Netw. 1998 Sep;9(3):221-31.
10
Deficiencies in progenitor cells of multiple hematopoietic lineages and defective megakaryocytopoiesis in mice lacking the thrombopoietic receptor c-Mpl.缺乏血小板生成受体c-Mpl的小鼠中多种造血谱系祖细胞的缺陷及巨核细胞生成缺陷。
Blood. 1996 Mar 15;87(6):2162-70.

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Sci Rep. 2015 Dec 21;5:18519. doi: 10.1038/srep18519.
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Dissection of vertebrate hematopoiesis using zebrafish thrombopoietin.利用斑马鱼血小板生成素对脊椎动物造血进行剖析。
Blood. 2014 Jul 10;124(2):220-8. doi: 10.1182/blood-2014-03-564682. Epub 2014 May 28.
3
Zinc transporters ZnT1 (Slc30a1), Zip8 (Slc39a8), and Zip10 (Slc39a10) in mouse red blood cells are differentially regulated during erythroid development and by dietary zinc deficiency.
小鼠红细胞中的锌转运蛋白ZnT1(Slc30a1)、Zip8(Slc39a8)和Zip10(Slc39a10)在红细胞发育过程中以及因饮食锌缺乏而受到不同程度的调节。
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