Chihara J, Nakajima S
Fourth Department of Internal Medicine, Kinki University School of Medicine, Osakasayama, Japan.
Nihon Kyobu Shikkan Gakkai Zasshi. 1993 Dec;31 Suppl:165-71.
Several characteristics of human eosinophil heterogeneity, as well as the existence of eosinophil subpopulations, "normodense" and "hypodense", have been reported in diseases associated with hypereosinophilia. Hypodense eosinophils can be distinguished by the increased expression of various membrane receptors including IL-5 receptor (J Exp Med 172: 1347) and various protein expression (J Immunol 142: 4416). On the other hand, recently, adhesion molecules are considered to play an important role in inflammatory processes in allergic and immune reactions such as bronchial asthma. Thus, in thin study, we examined the characteristics of expression of adhesion molecules on human eosinophils obtained from patients with hypereosinophila (hypodense eosinophils). As a result, high intensity expression of adhesion molecules (CR3, LFA-1 alpha, LFA-beta) on eosinophils were observed. Furthermore, ICAM-1, which is the ligand for LFA-1 molecules, was also expressed on eosinophils with hypereosinophilia. To extend our understanding of high intensity expression of adhesion molecules (CR3, LFA-1 alpha, LFA-1 beta, ICAM-1) on hypodense eosinophils, we examined whether chemotactic agents or eosinophilopoietic growth lymphokines (IL-3, GM-CSF, IL-5) are involved in adhesion molecule expression using an eosinophilic cell line, EoL-3. The expression of adhesion molecules on eosinophils was induced by some chemotactic agents and eosinophilopoietic growth lymphokines. Taken together, we conclude that eosinophilopoietic lymphokines as well as chemotactic agents may be involved in the high intensity expression of adhesion molecules on hypodense eosinophils.(ABSTRACT TRUNCATED AT 250 WORDS)
在与嗜酸性粒细胞增多相关的疾病中,已经报道了人类嗜酸性粒细胞异质性的几个特征,以及“正常密度”和“低密度”嗜酸性粒细胞亚群的存在。低密度嗜酸性粒细胞可通过包括白细胞介素-5受体(《实验医学杂志》172: 1347)在内的各种膜受体表达增加以及各种蛋白质表达(《免疫学杂志》142: 4416)来区分。另一方面,最近,黏附分子被认为在诸如支气管哮喘等过敏和免疫反应的炎症过程中起重要作用。因此,在本研究中,我们检测了从嗜酸性粒细胞增多患者中获得的人类嗜酸性粒细胞(低密度嗜酸性粒细胞)上黏附分子的表达特征。结果,观察到嗜酸性粒细胞上黏附分子(CR3、淋巴细胞功能相关抗原-1α、淋巴细胞功能相关抗原-β)的高强度表达。此外,作为淋巴细胞功能相关抗原-1分子配体的细胞间黏附分子-1也在嗜酸性粒细胞增多的嗜酸性粒细胞上表达。为了进一步了解低密度嗜酸性粒细胞上黏附分子(CR3、淋巴细胞功能相关抗原-1α、淋巴细胞功能相关抗原-1β、细胞间黏附分子-1)的高强度表达,我们使用嗜酸性细胞系EoL-3检测趋化剂或嗜酸性粒细胞生成生长淋巴因子(白细胞介素-3、粒细胞-巨噬细胞集落刺激因子、白细胞介素-5)是否参与黏附分子表达。嗜酸性粒细胞上黏附分子的表达可由一些趋化剂和嗜酸性粒细胞生成生长淋巴因子诱导。综上所述,我们得出结论,嗜酸性粒细胞生成淋巴因子以及趋化剂可能参与低密度嗜酸性粒细胞上黏附分子的高强度表达。(摘要截选至250词)