首页> 美国卫生研究院文献>Cell Transplantation >Wharton’s Jelly Mesenchymal Stromal Cells Support the Expansion of Cord Blood–derived CD34+ Cells Mimicking a Hematopoietic Niche in a Direct Cell–cell Contact Culture System
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Wharton’s Jelly Mesenchymal Stromal Cells Support the Expansion of Cord Blood–derived CD34+ Cells Mimicking a Hematopoietic Niche in a Direct Cell–cell Contact Culture System

机译:沃顿商学院的果冻间质基质细胞支持直接细胞间接触培养系统中模仿造血功能的脐血来源CD34 +细胞的扩增

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摘要

Wharton’s jelly mesenchymal stromal cells (WJ-MSCs) have been recently exploited as a feeder layer in coculture systems to expand umbilical cord blood–hematopoietic stem/progenitor cells (UCB-HSPCs). Here, we investigated the role of WJ-MSCs in supporting ex vivo UCB-HSPC expansion either when cultured in direct contact (DC) with WJ-MSCs or separated by a transwell system or in the presence of WJ-MSC–conditioned medium. We found, in short-term culture, a greater degree of expansion of UCB-CD34+ cells in a DC system (15.7 ± 4.1-fold increase) with respect to the other conditions. Moreover, in DC, we evidenced two different CD34+ cell populations (one floating and one adherent to WJ-MSCs) with different phenotypic and functional characteristics. Both multipotent CD34+/CD38 and lineage-committed CD34+/CD38+ hematopoietic progenitors were expanded in a DC system. The former were significantly more represented in the adherent cell fraction than in the floating one (18.7 ± 11.2% vs. 9.7 ± 7.9% over the total CD34+ cells). Short-term colony forming unit (CFU) assays showed that HSPCs adherent to the stromal layer were able to generate a higher frequency of immature colonies (CFU-granulocyte/macrophage and burst-forming unit erythroid/large colonies) with respect to the floating cells. In the attempt to identify molecules that may play a role in supporting the observed ex vivo HSPC growth, we performed secretome analyses. We found a number of proteins involved in the HSPC homing, self-renewal, and differentiation in all tested conditions. It is important to note that a set of sixteen proteins, which are only in part reported to be expressed in any hematopoietic niche, were exclusively found in the DC system secretome. In conclusion, WJ-MSCs allowed a significant ex vivo expansion of multipotent as well as committed HSPCs. This may be relevant for future clinical applications.
机译:沃顿商学院的果冻间质干细胞(WJ-MSC)最近被用作共培养系统的饲养层,以扩增脐带血-造血干/祖细胞(UCB-HSPC)。在这里,我们研究了WJ-MSC在支持与WJ-MSC直接接触(DC)或通过Transwell系统分开或存在WJ-MSC条件的培养基中分离时支持离体UCB-HSPC扩展的作用。我们发现,在短期培养中,相对于其他条件,DC系统中UCB-CD34 + 细胞的扩增程度更高(增加了15.7±4.1倍)。此外,在DC中,我们证实了两个不同的CD34 + 细胞群体(一个漂浮的细胞和一个粘附于WJ-MSC的细胞)具有不同的表型和功能特征。多能CD34 + / CD38 -和沿袭承诺的CD34 + / CD38 + 造血祖细胞均在直流系统。前者在粘附细胞中的比例明显高于在漂浮细胞中的比例(占总CD34 + 细胞的18.7±11.2%比9.7±7.9%)。短期菌落形成单位(CFU)分析表明,粘附于基质层的HSPC能够产生相对于漂浮细胞更高频率的未成熟菌落(CFU-粒细胞/巨噬细胞和爆发形成单位红系/大菌落) 。为了鉴定可能在支持观察到的离体HSPC生长中起作用的分子,我们进行了分泌组分析。我们发现在所有测试条件下,许多蛋白质都参与了HSPC归巢,自我更新和分化。重要的是要注意,仅在DC系统分泌组中发现了一组16种蛋白质,这些蛋白质仅部分报道在任何造血生态位中表达。总而言之,WJ-MSC允许多能和定型HSPC的显着体外扩增。这可能与将来的临床应用有关。

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