Smith P C, Cáceres M, Martínez C, Oyarzún A, Martínez J
School of Dentistry, Faculty of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile
Molecular and Cell Biology Program, Faculty of Medicine, University of Chile, Santiago, Chile.
J Dent Res. 2015 Mar;94(3):395-402. doi: 10.1177/0022034514563750. Epub 2014 Dec 19.
Gingival wound healing comprises a series of sequential responses that allow the closure of breaches in the masticatory mucosa. This process is of critical importance to prevent the invasion of microbes or other agents into tissues, avoiding the establishment of a chronic infection. Wound healing may also play an important role during cell and tissue reaction to long-term injury, as it may occur during inflammatory responses and cancer. Recent experimental data have shown that gingival wound healing is severely affected by the aging process. These defects may alter distinct phases of the wound-healing process, including epithelial migration, granulation tissue formation, and tissue remodeling. The cellular and molecular defects that may explain these deficiencies include several biological responses such as an increased inflammatory response, altered integrin signaling, reduced growth factor activity, decreased cell proliferation, diminished angiogenesis, reduced collagen synthesis, augmented collagen remodeling, and deterioration of the proliferative and differentiation potential of stem cells. In this review, we explore the cellular and molecular basis of these defects and their possible clinical implications.
牙龈伤口愈合包括一系列连续的反应,这些反应可使咀嚼黏膜中的创口闭合。这一过程对于防止微生物或其他病原体侵入组织、避免慢性感染的发生至关重要。在细胞和组织对长期损伤的反应过程中,如在炎症反应和癌症期间,伤口愈合也可能发挥重要作用。最近的实验数据表明,牙龈伤口愈合受到衰老过程的严重影响。这些缺陷可能会改变伤口愈合过程的不同阶段,包括上皮迁移、肉芽组织形成和组织重塑。可能解释这些缺陷的细胞和分子缺陷包括几种生物学反应,如炎症反应增加、整合素信号改变、生长因子活性降低、细胞增殖减少、血管生成减少、胶原蛋白合成减少、胶原蛋白重塑增加以及干细胞增殖和分化潜能的恶化。在这篇综述中,我们探讨了这些缺陷的细胞和分子基础及其可能的临床意义。