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Jagged 1的基质表达促进胎儿造血祖细胞的集落形成。

Stromal expression of Jagged 1 promotes colony formation by fetal hematopoietic progenitor cells.

作者信息

Jones P, May G, Healy L, Brown J, Hoyne G, Delassus S, Enver T

机构信息

Section of Gene Function and Regulation & Leukaemia Research Fund Centre, Chester Beatty Laboratories, Institute of Cancer Research, London, UK.

出版信息

Blood. 1998 Sep 1;92(5):1505-11.

PMID:9716576
Abstract

The Notch signaling system regulates proliferation and differentiation in many tissues. Notch is a transmembrane receptor activated by ligands expressed on adjacent cells. Hematopoietic stem cells and early progenitors express Notch, making the stromal cells which form cell-cell contacts with progenitor cells candidate ligand-presenting cells in the hematopoietic microenvironment. Therefore, we examined primary stromal cell cultures for expression of Notch ligands. Using reverse transcription-polymerase chain reaction, in situ hybridization, immunohistochemistry, and Western blotting, we demonstrate expression of Jagged 1 in primary stromal cultures. To investigate if the stromal expression of Jagged 1 has functional effects on hematopoietic progenitors, we cultured CD34(+), c-kit+ hematopoietic progenitor cells derived from the aorto gonadal mesonephros region of day 11 mouse embryos on the Jagged 1(-) stromal cell line S17 and on S17 cells engineered to express Jagged 1. The presence of Jagged 1 increased the number of colonies formed in subsequent methylcellulose culture fourfold. Larger increases in colony numbers were observed under the same culture conditions with CD34(+), c-kit+ hematopoietic progenitor cells derived from d11 fetal liver. These results obtained in vitro table Jagged 1 as a candidate regulator of stem cell fate in the context of stromal microenvironments in vivo.

摘要

Notch信号系统调节许多组织中的增殖和分化。Notch是一种跨膜受体,由相邻细胞表达的配体激活。造血干细胞和早期祖细胞表达Notch,使得与祖细胞形成细胞间接触的基质细胞成为造血微环境中候选的配体呈递细胞。因此,我们检测了原代基质细胞培养物中Notch配体的表达。通过逆转录-聚合酶链反应、原位杂交、免疫组织化学和蛋白质印迹法,我们证明了Jagged 1在原代基质培养物中的表达。为了研究Jagged 1的基质表达是否对造血祖细胞有功能影响,我们将来自第11天小鼠胚胎主动脉性腺中肾区域的CD34(+)、c-kit+造血祖细胞培养在Jagged 1(-)基质细胞系S17和经基因工程改造以表达Jagged 1的S17细胞上。Jagged 1的存在使随后甲基纤维素培养中形成的集落数量增加了四倍。在相同培养条件下,用来自第11天胎肝的CD34(+)、c-kit+造血祖细胞观察到集落数量有更大增加。这些体外获得的结果表明,Jagged 1是体内基质微环境中干细胞命运的候选调节因子。

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