Miller B E, Krasney P A, Gauvin D M, Holbrook K B, Koonz D J, Abruzzese R V, Miller R E, Pagani K A, Dolle R E, Ator M A
Department of Inflammation Pharmacology, Sterling Winthrop Pharmaceuticals Research Division, Collegeville, PA 19426.
J Immunol. 1995 Feb 1;154(3):1331-8.
The proinflammatory cytokine IL-1 beta is synthesized by activated monocytes and macrophages as a 31-kDa, biologically inactive precursor that is proteolytically processed to the biologically active 17-kDa mature molecule by the IL-1 beta converting enzyme (ICE). WIN 67694, Z-Val-Ala-Asp-CH2O(CO)[2,6-(CI2)]Ph, is a potent, selective inhibitor of human ICE. In activated murine peritoneal macrophages, WIN 67694 inhibited the release of mature IL-1 beta with an IC50 of 1.8 microM without any effect on the release of IL-1 alpha, IL-6, or TNF-alpha. The effect was specific to mature IL-1 beta release; the ICE inhibitor did not effect IL-1 beta RNA levels or precursor protein synthesis. In vivo, WIN 67694 was also able to inhibit selectively the release of IL-1 beta in a dose-dependent manner in a subcutaneous tissue chamber implant model of inflammation. IL-1 beta levels in tissue chamber fluid were inhibited 35 and 55% at 10 and 100 mg/kg, respectively. IL-1 alpha, IL-6, and TNF-alpha levels were not affected. The ability to selectively inhibit mature IL-1 beta release in vivo with ICE inhibitors will allow for detailed studies of the role of IL-1 beta and ICE in inflammatory diseases.
促炎细胞因子白细胞介素-1β(IL-1β)由活化的单核细胞和巨噬细胞合成,以31 kDa的生物无活性前体形式存在,该前体被白细胞介素-1β转化酶(ICE)蛋白水解加工成具有生物活性的17 kDa成熟分子。WIN 67694,Z-缬氨酸-丙氨酸-天冬氨酸-CH2O(CO)[2,6-(CI2)]苯,是一种有效的、选择性的人ICE抑制剂。在活化的小鼠腹腔巨噬细胞中,WIN 67694抑制成熟IL-1β的释放,IC50为1.8 μM,而对IL-1α、IL-6或肿瘤坏死因子-α(TNF-α)的释放没有任何影响。该作用对成熟IL-1β的释放具有特异性;ICE抑制剂对IL-1β RNA水平或前体蛋白合成没有影响。在体内,在炎症的皮下组织腔植入模型中,WIN 67694也能够以剂量依赖的方式选择性抑制IL-1β的释放。在10和100 mg/kg时,组织腔液中的IL-1β水平分别被抑制35%和55%。IL-1α、IL-6和TNF-α水平未受影响。使用ICE抑制剂在体内选择性抑制成熟IL-1β释放的能力将有助于详细研究IL-1β和ICE在炎症性疾病中的作用。