Menger M D, Vollmar B
Institute for Clinical and Experimental Surgery, University of Saarland, Homburg/Saar, Germany.
Br J Surg. 1996 May;83(5):588-601. doi: 10.1002/bjs.1800830506.
Cellular adhesion is mediated by distinct cell surface receptors (adhesion molecules) and plays a pivotal role in the biological processes of morphogenesis, cell migration and cell-cell communication. During the past decade many adhesion molecules have been identified and structurally analysed. This has allowed an understanding of their role in the pathophysiology of disease, including inflammation and sepsis, ischaemia and reperfusion, transplant rejection, atherosclerosis and thrombosis, angiogenesis and wound healing, as well as carcinogenesis and tumour metastasis. Understanding of the molecular mechanisms of cellular communication is not only vital for advances in surgical pathophysiology, it also has the potential to widen the spectrum of diagnosis and therapy of disease. Analysis of expression of individual surface molecules may help in the diagnosis of transplant rejection and allow a prognostic determination of tumour progression and metastasis formation. Moreover, manipulation of adhesion molecule function by monoclonal antibodies, antisense oligonucleotides or single gene products may open the door for novel therapeutic regimens to prevent transplant rejection and ischaemia-, sepsis- and shock-induced tissue injury.
细胞黏附由独特的细胞表面受体(黏附分子)介导,在形态发生、细胞迁移和细胞间通讯等生物学过程中起关键作用。在过去十年中,许多黏附分子已被鉴定并进行了结构分析。这使得人们能够了解它们在疾病病理生理学中的作用,包括炎症和脓毒症、缺血和再灌注、移植排斥、动脉粥样硬化和血栓形成、血管生成和伤口愈合,以及致癌作用和肿瘤转移。了解细胞通讯的分子机制不仅对手术病理生理学的进展至关重要,还具有拓宽疾病诊断和治疗范围的潜力。分析单个表面分子的表达可能有助于诊断移植排斥,并对肿瘤进展和转移形成进行预后判定。此外,通过单克隆抗体、反义寡核苷酸或单一基因产物操纵黏附分子功能,可能为预防移植排斥以及缺血、脓毒症和休克引起的组织损伤的新型治疗方案打开大门。