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[骨形态发生蛋白激活骨骼肌自身间充质干细胞以挽救骨髓衰竭]

[Activation of auto-mesenchymal stem cells of skeletal muscle by bone morphogenetic protein for rescuing bone marrow failure].

作者信息

Chu Jian-xin, Zhao Jun-ming, Ding Shun-li, Xu Shi-cai, Liu Ai-ru, Wang Shu-ping

机构信息

National Lab. of Experimental Hematology, Institute of Hematology, CAMS and PUMC, Tianjin, 300020, China.

出版信息

Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2002 Jun;24(3):272-5.

Abstract

OBJECTIVE

To explore the effect of bone morphogenetic protein (BMP) to activate mesenchymal stem cells of skeletal muscle for rescuing bone marrow failure.

METHODS

The study was performed on lethal rat acute aplastic anemia model induced by combined 5-fluorouracil (5-FU) and busulfan. The rh-BMP-2 was implanted into the thigh muscle of the rats at 3 days before aplastic anemia was induced. In the control group the rats were implanted with agar into the thigh muscle. The blood picture, pathologic changes and the mortality in two groups were observed. At the same time, rh-BMP-2 were implanted into the thigh muscle of normal Kun-min mice for dynamic control observation of the implantation local morphological changes, colony forming units-spleen (CFU-S) and stem cell growth factor (SCF) expression of the stroma cells of ectopic ossicles induced by BMP.

RESULTS

At 7 days after BMP implantation in the mice the mesenchymal cells around BMP in muscle proliferated, and appeared in bone marrow to form an ectopic ossicles. The SCF expression of stroma cells in ectopic ossicles were higher than that of self-bone marrow. 56.3% of BMP-treated aplastic rats were survived over 3 months and its hematopoiesis was completely reconstituted and the histo-morphological picture of the spleen and bone marrow were recovered to normal. But in the control group only one of 23 rats was survived, the remainder died of hematopoietic failure.

CONCLUSIONS

BMP-implantation into the skeletal muscle could rescue the bone marrow hematopoietic failure. The mechanism might be related to the BMP activated auto-mesenchymal cells of skeletal muscles to direct hematopoietic cell differentiation. In our hands it might create a new pathway for utilization of auto-muscle derived mesenchymal cells to reconstitute hematopoiesis.

摘要

目的

探讨骨形态发生蛋白(BMP)激活骨骼肌间充质干细胞以挽救骨髓衰竭的作用。

方法

以5-氟尿嘧啶(5-FU)和白消安联合诱导建立致死性大鼠急性再生障碍性贫血模型。在诱导再生障碍性贫血前3天,将重组人骨形态发生蛋白-2(rh-BMP-2)植入大鼠大腿肌肉。对照组大鼠大腿肌肉植入琼脂。观察两组大鼠的血象、病理变化及死亡率。同时,将rh-BMP-2植入正常昆明小鼠大腿肌肉,动态对照观察植入部位局部形态变化、骨形态发生蛋白诱导异位骨的脾集落形成单位(CFU-S)及基质细胞干细胞生长因子(SCF)表达。

结果

小鼠植入骨形态发生蛋白后7天,肌肉中骨形态发生蛋白周围的间充质细胞增殖,并出现在骨髓中形成异位骨。异位骨中基质细胞的干细胞生长因子表达高于自身骨髓。56.3%接受骨形态发生蛋白治疗的再生障碍性贫血大鼠存活超过3个月,其造血功能完全重建,脾脏和骨髓的组织形态恢复正常。但对照组23只大鼠中仅1只存活,其余死于造血衰竭。

结论

将骨形态发生蛋白植入骨骼肌可挽救骨髓造血衰竭。其机制可能与骨形态发生蛋白激活骨骼肌自身间充质细胞以指导造血细胞分化有关。在我们的研究中,这可能为利用自体肌肉来源的间充质细胞重建造血创造一条新途径。

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