Surgery Service, Virgen de La Arrixaca University Clinical Hospital, El Palmar, Murcia, Spain.
Molecular Oncology and TGF-ß, Research Unit, Virgen de La Arrixaca University Hospital, El Palmar, Murcia, Spain.
Placenta. 2017 Nov;59:146-153. doi: 10.1016/j.placenta.2017.04.005. Epub 2017 Apr 10.
Wound healing usually follows a predictable sequence and prognosis of events. Its evolutionary process is the result of a complicated interaction between patient-related factors, the wound, the treatment used and the skills and knowledge of the professionals who treat them. Only through a meticulous initial assessment of the wound is it possible to identify the factors that contribute to its complexity. The challenge for professionals will be to implement efficient therapies at the right time and in the most cost-efficient way in order to reduce associated problems, treat the symptoms and expectations of the patients and achieve adequate wound healing whenever possible. This is particularly evident in big chronic wounds with considerable tissue loss, which become senescent in the process of inflammation or proliferation losing the ability to epithelialize. Generally, chronic wounds do not respond to current treatments, therefore they need special interventions. AM is a tissue of particular interest as a biological dressing and it has well-documented reepithelialization effects which are in part related to its capacity to synthesize and release biological active factors. Our studies have demonstrated that amniotic membrane (AM) is able to induce epithelialization in chronic wounds that were unable to epithelialize. AM induces several signaling pathways that are involved in cell migration and/or proliferation. Additionally, AM is able to selectively antagonize the anti-proliferative effect of transforming growth factor-ß (TGF-β) by modifying the genetic program that TGF-β induces on keratinocytes. The combined effect of AM on keratinocytes, promoting cell proliferation/migration and antagonizing the effect of TGF-β is the perfect combination, allowing chronic wounds to move out of their non-healing state and progress into epithelialization.
伤口愈合通常遵循可预测的顺序和事件预后。其演变过程是患者相关因素、伤口、所采用的治疗方法以及治疗它们的专业人员的技能和知识之间复杂相互作用的结果。只有通过对伤口进行细致的初步评估,才能确定导致其复杂性的因素。专业人员的挑战将是在正确的时间以最具成本效益的方式实施有效的治疗,以减少相关问题、治疗患者的症状和期望,并尽可能实现适当的伤口愈合。这在具有大量组织损失的大型慢性伤口中尤为明显,这些伤口在炎症或增殖过程中会衰老,失去上皮化的能力。一般来说,慢性伤口对当前的治疗方法没有反应,因此需要特殊干预。AM 是一种特别有趣的组织,作为生物敷料,它具有很好的上皮化作用,这在一定程度上与其合成和释放生物活性因子的能力有关。我们的研究表明,羊膜(AM)能够诱导无法上皮化的慢性伤口上皮化。AM 诱导几种参与细胞迁移和/或增殖的信号通路。此外,AM 能够通过修饰 TGF-β 诱导角质形成细胞的遗传程序,选择性拮抗 TGF-β 的抗增殖作用。AM 对角质形成细胞的综合作用,促进细胞增殖/迁移并拮抗 TGF-β 的作用,是一种完美的组合,使慢性伤口能够摆脱其不愈合状态并进入上皮化阶段。