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体内E-选择素和P-选择素表达的异质性。

Heterogeneity of expression of E- and P-selectins in vivo.

作者信息

Eppihimer M J, Wolitzky B, Anderson D C, Labow M A, Granger D N

机构信息

Department of Physiology and Biophysics, Louisiana State University Medical Center, Shreveport, USA.

出版信息

Circ Res. 1996 Sep;79(3):560-9. doi: 10.1161/01.res.79.3.560.

Abstract

A novel technique involving radiolabeled monoclonal antibodies was used to characterize and compare the expression of E- and P-selectin on unstimulated, histamine-challenged, and endotoxin-challenged endothelial cells in various tissues of the mouse. Under unstimulated conditions, E-selectin was absent in all organs, but significant expression of P-selectin was observed in several organs. Histamine induced a rapid time-dependent upregulation of P-selectin, with the largest responses observed in mesentery and lung. Significant fold elevations in P-selectin expression occurred as early as 5 minutes after the histamine injection and remained elevated up to 1 hour. Histamine-induced P-selectin upregulation was inhibited by the H1 receptor antagonist diphenhydramine, whereas the H2 receptor antagonist cimetidine had no effect. Endotoxin (lipopolysaccharide [LPS]) also induced a time-dependent expression of P-selectin that reached a maximum between 4 and 8 hours after endotoxin administration. LPS-induced upregulation of P-selectin was greatest in heart and stomach, which exhibited insignificant constitutive expression of P-selectin. LPS also induced a time-dependent upregulation of E-selectin, with maximal expression occurring 3 to 5 hours after intraperitoneal administration. The lung and small intestine exhibited the largest responses to LPS challenge. Histamine administration did not affect E-selectin expression in any tissue. E- and P-selectin-deficient mice were used to test the specificity of monoclonal antibody binding in unstimulated, histamine-challenged, and LPS-stimulated tissues. Vascular binding of the radiolabeled E-selectin and P-selectin monoclonal antibodies was not observed in the respective deficient mice. These findings suggest that P-selectin is constitutively expressed on vascular endothelium in some tissues of the mouse and that there are significant regional differences in the magnitude and time course of histamine- and endotoxin-induced P-selectin expression. In contrast, E-selectin appears to be absent on unstimulated vascular endothelium but is upregulated within 3 hours after the administration of endotoxin in most tissues.

摘要

一种涉及放射性标记单克隆抗体的新技术被用于表征和比较小鼠不同组织中未受刺激、组胺激发及内毒素激发的内皮细胞上E-选择素和P-选择素的表达。在未受刺激的条件下,所有器官中均未检测到E-选择素,但在几个器官中观察到了P-选择素的显著表达。组胺诱导了P-选择素的快速时间依赖性上调,在肠系膜和肺中观察到的反应最大。早在注射组胺后5分钟,P-选择素表达就出现了显著的倍数升高,并持续升高至1小时。组胺诱导的P-选择素上调被H1受体拮抗剂苯海拉明抑制,而H2受体拮抗剂西咪替丁则无作用。内毒素(脂多糖[LPS])也诱导了P-选择素的时间依赖性表达,在内毒素给药后4至8小时达到最大值。LPS诱导的P-选择素上调在心脏和胃中最为显著,这两个器官中P-选择素的组成性表达不明显。LPS还诱导了E-选择素的时间依赖性上调,腹腔注射后3至5小时出现最大表达。肺和小肠对LPS激发的反应最大。组胺给药对任何组织中的E-选择素表达均无影响。使用E-和P-选择素缺陷小鼠来测试未受刺激、组胺激发及LPS刺激组织中单克隆抗体结合的特异性。在各自的缺陷小鼠中未观察到放射性标记的E-选择素和P-选择素单克隆抗体的血管结合。这些发现表明,P-选择素在小鼠的一些组织中的血管内皮细胞上组成性表达,并且组胺和内毒素诱导的P-选择素表达的幅度和时间进程存在显著的区域差异。相比之下,E-选择素在未受刺激的血管内皮细胞上似乎不存在,但在大多数组织中,内毒素给药后3小时内会上调。

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