Demidova-Rice Tatiana N, Durham Jennifer T, Herman Ira M
Department of Radiation Oncology, Edwin L. Steele Laboratory for Tumor Biology, Massachusetts General Hospital , Boston, MA 02114.
Department of Molecular Physiology and Pharmacology and the Center for Innovations in Wound Healing Research, Tufts University School of Medicine and Graduate Program in Cellular and Molecular Physiology, Sackler School of Graduate Biomedical Sciences, Tufts University , Boston, MA 02111.
Adv Wound Care (New Rochelle). 2012 Feb;1(1):17-22. doi: 10.1089/wound.2011.0308.
Formation of new blood vessels, by either angiogenesis or vasculogenesis, is critical for normal wound healing. Major processes in neovascularization include (i) growth-promoting or survival factors, (ii) proteolytic enzymes, (iii) activators of multiple differentiated and progenitor cell types, and (iv) permissible microenvironments. A central aim of wound healing research is to "convert" chronic, disease-impaired wounds into those that will heal.
Reduced ability to re-establish a blood supply to the injury site can ultimately lead to wound chronicity.
BASIC/CLINICAL SCIENCE ADVANCES: (1) Human fetal endothelial progenitor cells can stimulate wound revascularization and repair following injury, as demonstrated in a novel mouse model of diabetic ischemic healing. (2) Advances in bioengineering reveal exciting alternatives by which wound repair may be facilitated via the creation of vascularized microfluidic networks within organ constructs created for wound implantation. (3) A "personalized" approach to regenerative medicine may be enabled by the identification of protein components present within individual wound beds, both chronic and acute.
Despite the development of numerous therapies, impaired angiogenesis and wound chronicity remain significant healthcare problems. As such, innovations in enhancing wound revascularization would lead to significant advances in wound healing therapeutics and patient care.
Insights into endothelial progenitor cell biology together with developments in the field of tissue engineering and molecular diagnostics should not only further advance our understanding of the molecular mechanisms regulating wound repair but also offer innovative solutions to promote the healing of chronic and acute wounds .
通过血管生成或血管发生形成新血管对于正常伤口愈合至关重要。新血管形成的主要过程包括:(i)生长促进或存活因子;(ii)蛋白水解酶;(iii)多种分化细胞和祖细胞类型的激活剂;(iv)适宜的微环境。伤口愈合研究的一个核心目标是将慢性、疾病损伤的伤口“转化”为能够愈合的伤口。
重新建立损伤部位血液供应的能力降低最终可能导致伤口慢性化。
基础/临床科学进展:(1)在一种新型糖尿病缺血性愈合小鼠模型中证实,人胎儿内皮祖细胞可刺激损伤后伤口的血管再形成和修复。(2)生物工程学的进展揭示了令人兴奋的替代方法,即通过在为伤口植入而构建的器官结构内创建血管化微流体网络来促进伤口修复。(3)通过识别慢性和急性伤口床中存在的蛋白质成分,可能实现再生医学的“个性化”方法。
尽管开发了多种治疗方法,但血管生成受损和伤口慢性化仍然是重大的医疗问题。因此,增强伤口血管再形成方面的创新将导致伤口愈合治疗和患者护理取得重大进展。
对内皮祖细胞生物学的深入了解以及组织工程和分子诊断领域的发展,不仅应进一步增进我们对调节伤口修复分子机制的理解,还应提供促进慢性和急性伤口愈合的创新解决方案。