Cellular Reprogramming and Embryo Biotechnology Laboratory, Dental Research Institute, Seoul National University School of Dentistry, Seoul 08826, Korea.
Department of Bioengineering and QB3 Institute, University of California, Berkeley, CA 94720, USA.
Molecules. 2021 May 1;26(9):2658. doi: 10.3390/molecules26092658.
Salivary gland stem cells (SGSCs) are potential cell sources for the treatment of salivary gland diseases. The control of cell survival is an essential factor for applying stem cells to regenerative medicine or stem cell-based research. The purpose of this study was to investigate the effects of the ROCK inhibitor Y-27632 on the survival of SGSCs and its underlying mechanisms. SGSCs were isolated from mouse submandibular glands and cultured in suspension. Treatment with Y-27632 restored the viability of SGSCs that was significantly decreased during isolation and the subsequent culture. Y-27632 upregulated the expression of anti-apoptotic protein BCL-2 in SGSCs and, in the apoptosis assay, significantly reduced apoptotic and necrotic cell populations. Matrigel was used to mimic the extracellular environment of an intact salivary gland. The expression of genes regulating apoptosis and the ROCK signaling pathway was significantly reduced when SGSCs were embedded in Matrigel. SGSCs cultured in Matrigel and treated with Y-27632 showed no difference in the total numbers of spheroids and expression levels of apoptosis-regulating genes. Matrigel-embedded SGSCs treated with Y-27632 increased the number of spheroids with budding structures and the expression of acinar cell-specific marker AQP5. We demonstrate the protective effects of Y-27632 against dissociation-induced apoptosis of SGSCs during their culture in vitro.
唾液腺干细胞(SGSCs)是治疗唾液腺疾病的潜在细胞来源。细胞存活的控制是将干细胞应用于再生医学或基于干细胞的研究的一个重要因素。本研究旨在探讨 ROCK 抑制剂 Y-27632 对 SGSCs 存活的影响及其潜在机制。从小鼠颌下腺中分离 SGSCs 并在悬浮液中培养。Y-27632 处理可恢复在分离和随后的培养过程中明显降低的 SGSCs 的活力。Y-27632 上调了 SGSCs 中抗凋亡蛋白 BCL-2 的表达,在凋亡测定中,明显减少了凋亡和坏死细胞群体。Matrigel 用于模拟完整唾液腺的细胞外环境。当 SGSCs 嵌入 Matrigel 中时,调节凋亡和 ROCK 信号通路的基因的表达显著降低。在 Matrigel 中培养并用 Y-27632 处理的 SGSCs 在总球体数量和凋亡调节基因的表达水平上没有差异。用 Y-27632 处理的嵌入 Matrigel 的 SGSCs 增加了具有萌芽结构的球体数量和腺泡细胞特异性标记物 AQP5 的表达。我们证明了 Y-27632 在体外培养过程中对 SGSCs 分离诱导的凋亡的保护作用。