Wardlaw A J, Walsh G M, Symon F A
Department of Respiratory Medicine, Leicester University Medical School, Glenfield Hospital, UK.
Ann N Y Acad Sci. 1996 Oct 31;796:124-37. doi: 10.1111/j.1749-6632.1996.tb32574.x.
Considerable progress has been made in our understanding of the molecular mechanisms involved in eosinophil migration into sites of allergic inflammation. A number of differences between eosinophils and neutrophils have been observed in their pattern of adhesion interactions. These include expression of alpha 4 beta 1, alpha 4 beta 7, and alpha 6 beta 1 by eosinophils but not neutrophils and structural differences between eosinophil and neutrophil PSGL-1 associated with increased eosinophil binding to P-selectin. On the basis of current evidence the various receptors and mediators involved are summarized in FIGURE 1. Once in the tissues eosinophils may persist for several days or weeks, surviving under the influence of locally generated cytokines and this persistence may also partly explain selective tissue accumulation of eosinophils. Understanding the molecular mechanisms involved in leucocyte migration offers the possibility of selective and effective antagonists to treat allergic disease by preventing cell migration. Results in a number of animal models already offer the hope that this approach may be successful. The development of drugs that can be tested in the clinic are awaited with considerable interest.
在我们对嗜酸性粒细胞迁移至变应性炎症部位所涉及的分子机制的理解方面已取得了相当大的进展。在嗜酸性粒细胞和中性粒细胞的黏附相互作用模式中已观察到许多差异。这些差异包括嗜酸性粒细胞表达α4β1、α4β7和α6β1,而中性粒细胞不表达,以及嗜酸性粒细胞和中性粒细胞PSGL-1之间的结构差异,这与嗜酸性粒细胞与P-选择素结合增加有关。根据目前的证据,图1总结了所涉及的各种受体和介质。一旦进入组织,嗜酸性粒细胞可能会持续存在数天或数周,在局部产生的细胞因子的影响下存活,这种持续性也可能部分解释了嗜酸性粒细胞在组织中的选择性积聚。了解白细胞迁移所涉及的分子机制为通过阻止细胞迁移来治疗变应性疾病提供了选择性和有效拮抗剂的可能性。一些动物模型的结果已经带来了这种方法可能成功的希望。人们怀着极大的兴趣期待着能够在临床上进行测试的药物的开发。