Gowtham A, Kaundal Ravinder K
Department of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research, Raebareli (NIPER-R), Transit Campus, Bijnor-Sisendi Road, Sarojini Nagar, Near CRPF Base Camp, Lucknow, UP 226002, India.
Department of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research, Raebareli (NIPER-R), Transit Campus, Bijnor-Sisendi Road, Sarojini Nagar, Near CRPF Base Camp, Lucknow, UP 226002, India.
Int J Biol Macromol. 2025 Mar;292:139206. doi: 10.1016/j.ijbiomac.2024.139206. Epub 2024 Dec 26.
Exosomal non-coding RNAs (ncRNAs), including miRNAs, lncRNAs, and circRNAs, have emerged as crucial modulators in cellular signaling, influencing wound healing processes. Stem cell-derived exosomes, which serve as vehicles for these ncRNAs, show remarkable therapeutic potential due to their ability to modulate wound healing stages, from initial inflammation to collagen formation. These ncRNAs act as molecular signals, regulating gene expression and protein synthesis necessary for cellular responses in healing. Wound healing is a complex, staged process involving inflammation, hemostasis, fibroblast proliferation, angiogenesis, and tissue remodeling. Stem cell-derived exosomal ncRNAs enhance these stages by reducing excessive inflammation, promoting anti-inflammatory responses, guiding fibroblast and keratinocyte maturation, enhancing vascularization, and ensuring organized collagen deposition. Their molecular cargo, particularly ncRNAs, specifically targets pathways to aid chronic wound repair and support scarless regeneration. This review delves into the unique composition and signaling roles of Stem cell-derived exosomes and ncRNAs, highlighting their impact across wound healing stages and their potential as innovative therapeutics. Understanding the interaction between exosomal ncRNAs and cellular signaling pathways opens new avenues in regenerative medicine, positioning Stem cell-derived exosomes and their ncRNAs as promising molecular-level interventions in wound healing.
外泌体非编码RNA(ncRNA),包括微小RNA(miRNA)、长链非编码RNA(lncRNA)和环状RNA(circRNA),已成为细胞信号传导中的关键调节因子,影响伤口愈合过程。干细胞衍生的外泌体作为这些ncRNA的载体,由于其能够调节从初始炎症到胶原蛋白形成的伤口愈合阶段,显示出显著的治疗潜力。这些ncRNA作为分子信号,调节愈合过程中细胞反应所需的基因表达和蛋白质合成。伤口愈合是一个复杂的、分阶段的过程,包括炎症、止血、成纤维细胞增殖、血管生成和组织重塑。干细胞衍生的外泌体ncRNA通过减少过度炎症、促进抗炎反应、引导成纤维细胞和角质形成细胞成熟、增强血管生成以及确保有组织的胶原蛋白沉积来促进这些阶段。它们的分子内容物,特别是ncRNA,特异性地靶向有助于慢性伤口修复和支持无瘢痕再生的途径。本综述深入探讨了干细胞衍生的外泌体和ncRNA的独特组成和信号作用,强调了它们在伤口愈合各阶段的影响及其作为创新疗法的潜力。了解外泌体ncRNA与细胞信号通路之间的相互作用为再生医学开辟了新途径,将干细胞衍生的外泌体及其ncRNA定位为伤口愈合中有前景的分子水平干预措施。