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健康志愿者骨髓内注射重组人可溶性组织因子激活的自体富血小板血浆后体内间充质基质细胞的生成。

In vivo production of mesenchymal stromal cells after injection of autologous platelet-rich plasma activated by recombinant human soluble tissue factor in the bone marrow of healthy volunteers.

机构信息

1 Department of Stomatology and Maxillo-Facial Surgery, HIS Site Bracops , Brussels, Belgium .

出版信息

Tissue Eng Part A. 2014 Jan;20(1-2):160-70. doi: 10.1089/ten.TEA.2013.0244. Epub 2013 Sep 24.

DOI:10.1089/ten.TEA.2013.0244
PMID:23924315
Abstract

Autologous mesenchymal stromal cell (MSC)-based therapies offer one of the most promising and safe methods for regeneration or reconstruction of tissues and organs. Routine procedures to obtain adequate amount of autologous stem cells need their expansion through culture, with risks of contamination and cell differentiation, leading to the loss of cell ability for therapies. We suggest the use of human bone marrow (BM) as a physiological bioreactor to produce autologous MSC by injection of autologous platelet-rich plasma activated by recombinant human soluble tissue factor (rhsTF) in iliac crest. A trial on 13 healthy volunteers showed the feasibility and harmlessness of the procedure. The phenotype and cellularity of BM cells were not modified, on day 3 after injection. Endothelial progenitor cells (EPC) were mobilized to the bloodstream, without stimulation of hematopoietic stem cells (HSC). MSC level in BM increased with a specific commitment to preosteoblastic cell population both in vivo and in vitro. This self-stimulation system of BM seems thus to be a promising feasible process 3 days before clinical cell therapy applications.

摘要

自体间充质基质细胞(MSC)疗法为组织和器官的再生或重建提供了最有前途和最安全的方法之一。获得足够数量的自体干细胞的常规程序需要通过培养来扩增它们,但存在污染和细胞分化的风险,导致细胞治疗能力丧失。我们建议使用人骨髓(BM)作为生理生物反应器,通过在髂嵴处注射由重组人可溶性组织因子(rhsTF)激活的自体富血小板血浆来产生自体 MSC。对 13 名健康志愿者的试验表明,该程序具有可行性且无害。注射后第 3 天,BM 细胞的表型和细胞数量没有改变。内皮祖细胞(EPC)被动员到血液中,而不会刺激造血干细胞(HSC)。MSC 水平在 BM 中增加,具有体内和体外向成骨前体细胞群的特定定向。因此,这种 BM 的自我刺激系统似乎是在临床细胞治疗应用前 3 天有希望可行的过程。

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