Department of Molecular Medicine, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Bergamo, Italy.
Both the authors are co-first author.
Cell Transplant. 2020 Jan-Dec;29:963689720965467. doi: 10.1177/0963689720965467.
Mesenchymal stromal cells (MSCs) are emerging as a novel therapeutic option for limiting chronic kidney disease progression. Conditioned medium (CM) containing bioactive compounds could convey similar benefits, avoiding the potential risks of cell therapy. This study compared the efficacy of nonrenal and renal cell-based therapy with the corresponding CM in rats with renal mass reduction (RMR). Infusions of human kidney stromal cells (kPSCs) and CM-kPSCs, but not umbilical cord (uc) MSCs or CM-ucMSCs, reduced proteinuria and preserved podocyte number and nephrin expression in RMR rats. Glomerular fibrosis, microvascular rarefaction, and apoptosis were reduced by all treatments, while the peritubular microvascular loss was reduced by kPSCs and CM-kPSCs treatment only. Importantly, kPSCs and CM-kPSCs reduced NG2-positive pericytes, and all therapies reduced α-smooth muscle actin expression, indicating reduced myofibroblast expansion. Treatment with kPSCs also significantly inhibited the accumulation of ED1-positive macrophages in the renal interstitium of RMR rats. These findings demonstrate that the CM of ucMSCs and kPSCs confers similar renoprotection as the cells. kPSCs and CM-kPSCs may be superior in attenuating chronic renal injury as a cell source.
间充质基质细胞(MSCs)作为一种限制慢性肾脏病进展的新型治疗选择正在出现。含有生物活性化合物的条件培养基(CM)可能具有类似的益处,同时避免细胞治疗的潜在风险。本研究比较了肾细胞和非肾细胞为基础的治疗方法与相应 CM 在肾部分切除(RMR)大鼠中的疗效。输注人肾基质细胞(kPSCs)和 CM-kPSCs 可减少蛋白尿,维持 RMR 大鼠足细胞数量和肾小囊蛋白表达,而脐带间充质干细胞(ucMSCs)或 CM-ucMSCs 则无此作用。所有治疗方法均可减少肾小球纤维化、微血管稀疏和细胞凋亡,而仅 kPSCs 和 CM-kPSCs 治疗可减少肾小管周围微血管丢失。重要的是,kPSCs 和 CM-kPSCs 减少了 NG2 阳性周细胞的数量,所有治疗方法均可减少α-平滑肌肌动蛋白的表达,表明肌成纤维细胞的扩张减少。kPSCs 治疗还可显著抑制 RMR 大鼠肾间质中 ED1 阳性巨噬细胞的积聚。这些发现表明,ucMSCs 和 kPSCs 的 CM 可提供类似的肾脏保护作用。kPSCs 和 CM-kPSCs 可能作为细胞来源,在减轻慢性肾损伤方面更具优势。