首页> 外文期刊>American Journal of Pathology: Official Publication of the American Association of Pathologists >Adipose tissue-derived mesenchymal stem cells facilitate hematopoiesis in vitro and in vivo: advantages over bone marrow-derived mesenchymal stem cells.
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Adipose tissue-derived mesenchymal stem cells facilitate hematopoiesis in vitro and in vivo: advantages over bone marrow-derived mesenchymal stem cells.

机译:脂肪组织来源的间充质干细胞在体外和体内促进造血作用:与骨髓来源的间充质干细胞相比具有优势。

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Mesenchymal stem cells (MSCs) have emerged as a new therapeutic modality for reconstituting the hematopoietic microenvironment by improving engraftment in stem cell transplantation. However, the availability of conventional bone marrow (BM)-derived MSCs (BMSCs) is limited. Recent studies showed that a large number of MSCs can be easily isolated from fat tissue (adipose tissue-derived MSCs [ADSCs]). In this study, we extensively evaluated the hematopoiesis-supporting properties of ADSCs, which are largely unknown. In vitro coculture and progenitor assays showed that ADSCs generated significantly more granulocytes and progenitor cells from human hematopoietic stem cells (HSCs) than BMSCs. We found that ADSCs express the chemokine CXCL12, a critical regulator of hematopoiesis, at levels that are three fold higher than those with BMSCs. The addition of a CXCL12 receptor antagonist resulted in a lower yield of granulocytes from ADSC layers, whereas the addition of recombinant CXCL12 to BMSC cocultures promoted the growth of granulocytes. In vivo cell homing assays showed that ADSCs facilitated the homing of mouse HSCs to the BM better than BMSCs. ADSCs injected into the BM cavity of fatally irradiated mice reconstituted hematopoiesis more promptly than BMSCs and subsequently rescued mice that had received a low number of HSCs. Secondary transplantation experiments showed that ADSCs exerted favorable effects on long-term HSCs. These results suggest that ADSCs can be a promising therapeutic alternative to BMSCs.
机译:间充质干细胞(MSCs)已成为通过改善干细胞移植中的植入来重建造血微环境的一种新的治疗方式。但是,常规骨髓(BM)衍生的MSC(BMSC)的可用性受到限制。最近的研究表明,可以容易地从脂肪组织(脂肪组织来源的MSC [ADSC])中分离出大量MSC。在这项研究中,我们广泛评估了ADSC的造血支持特性,这在很大程度上是未知的。体外共培养和祖细胞测定表明,ADSC从人造血干细胞(HSC)产生的粒细胞和祖细胞明显多于BMSC。我们发现ADSCs表达趋化因子CXCL12(一种造血关键调节剂)的水平比BMSCs高三倍。 CXCL12受体拮抗剂的添加导致ADSC层粒细胞的产量降低,而BMSC共培养物中添加重组CXCL12则促进了粒细胞的生长。体内细胞归巢测定表明,ADSC比BMSC更好地促进了小鼠HSC向BM的归巢。与BMSCs相比,将ADSCs注入到放射线照射的小鼠的BM腔中可以比造血干细胞更迅速地重建造血功能,并随后救出了接受了少量HSCs的小鼠。二次移植实验表明,ADSC对长期HSC具有良好的作用。这些结果表明,ADSCs可以成为BMSCs的有前途的治疗选择。

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