Program in Regenerative Medicine, Vascular Biology Group, Department of Physiology and Pharmacology, Krembil Centre for Stem Cell Biology, Robarts Research Institute, The University of Western Ontario, London, Ontario, Canada.
Stem Cells Dev. 2012 Jul 20;21(11):1863-76. doi: 10.1089/scd.2011.0634. Epub 2012 Apr 16.
Transplanted human bone marrow (BM) and umbilical cord blood (UCB) progenitor cells activate islet-regenerative or revascularization programs depending on the progenitor subtypes administered. Using purification of multiple progenitor subtypes based on a conserved stem cell function, high aldehyde dehydrogenase (ALDH) activity (ALDH(hi)), we have recently shown that transplantation of BM-derived ALDH(hi) progenitors improved systemic hyperglycemia and augmented insulin secretion by increasing islet-associated proliferation and vascularization, without increasing islet number. Conversely, transplantation of culture-expanded multipotent-stromal cells (MSCs) derived from BM ALDH(hi) cells augmented total beta cell mass via formation of beta cell clusters associated with the ductal epithelium, without sustained islet vascularization. To identify paracrine effectors produced by islet-regenerative MSCs, culture-expanded BM ALDH(hi) MSCs were transplanted into streptozotocin-treated nonobese diabetic/severe combine immune deficient (SCID) mice and segregated into islet-regenerative versus nonregenerative cohorts based on hyperglycemia reduction, and subsequently compared for differential production of mRNA and secreted proteins. Regenerative MSCs showed increased expression of matrix metalloproteases, epidermal growth factor receptor (EGFR)-activating ligands, and downstream effectors of Wnt signaling. Regenerative MSC supernatant also contained increased levels of pro-angiogenic versus pro-inflammatory cytokines, and augmented the expansion of ductal epithelial but not beta cells in vitro. Conversely, co-culture with UCB ALDH(hi) cells induced beta cell but not ductal epithelial cell proliferation. Sequential transplantation of MSCs followed by UCB ALDH(hi) cells improved hyperglycemia and glucose tolerance by increasing beta cell mass associated with the ductal epithelium and by augmenting intra-islet capillary densities. Thus, combinatorial human progenitor cell transplantation stimulated both islet-regenerative and revascularization programs. Understanding the progenitor-specific pathways that modulate islet-regenerative and revascularization processes may provide new approaches for diabetes therapy.
移植的人骨髓(BM)和脐血(UCB)祖细胞根据所施用的祖细胞亚型激活胰岛再生或血管生成程序。我们最近使用基于保守干细胞功能的多种祖细胞亚型的纯化,高醛脱氢酶(ALDH)活性(ALDH(hi)),表明移植 BM 衍生的 ALDH(hi)祖细胞通过增加胰岛相关的增殖和血管生成改善全身高血糖,并增强胰岛素分泌,而不增加胰岛数量。相反,移植源自 BM ALDH(hi)细胞的培养扩增多能基质细胞(MSCs)通过与导管上皮相关的 beta 细胞簇的形成增加总 beta 细胞质量,而不持续胰岛血管生成。为了鉴定胰岛再生 MSC 产生的旁分泌效应物,将培养扩增的 BM ALDH(hi) MSC 移植到链脲佐菌素处理的非肥胖型糖尿病/严重联合免疫缺陷(SCID)小鼠中,并根据高血糖降低将其分为胰岛再生与非再生队列,随后比较差异表达的 mRNA 和分泌蛋白。再生 MSC 显示基质金属蛋白酶、表皮生长因子受体(EGFR)激活配体和 Wnt 信号下游效应物的表达增加。再生 MSC 上清液还含有增加的促血管生成与促炎细胞因子,并在体外增加导管上皮但不增加 beta 细胞的扩张。相反,与 UCB ALDH(hi)细胞共培养诱导 beta 细胞但不诱导导管上皮细胞增殖。MSC 序贯移植后再移植 UCB ALDH(hi)细胞通过增加与导管上皮相关的 beta 细胞质量和增加胰岛内毛细血管密度来改善高血糖和葡萄糖耐量。因此,组合人祖细胞移植刺激胰岛再生和血管生成程序。了解调节胰岛再生和血管生成过程的祖细胞特异性途径可能为糖尿病治疗提供新方法。
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