Sweeney Zachary K, Minatti Ana, Button Donald C, Patrick Silvia
Department of Medicinal Chemistry, Genentech, Inc. 1 DNA Way, South San Francisco, CA 94080, USA.
ChemMedChem. 2009 May;4(5):706-18. doi: 10.1002/cmdc.200800452.
Controlled variation in intracellular calcium concentration is a key component of the immune response signaling pathway in lymphocytes. Store-operated calcium entry (SOCE) in these cells provides a prolonged increase in cytoplasmic Ca(2+) concentrations and ultimately leads to the production of pro-inflammatory cytokines. Molecules that inhibit SOCE could therefore be useful immunomodulating agents for the treatment of rheumatoid arthritis, psoriasis, inflammatory bowel disease, and other conditions. Although the presence of the SOCE signaling pathway in lymphocytes and other cells involved in the immune response has been known for many years, key proteins involved in SOCE were identified only recently. The identification of these proteins may further enable the identification of agents that inhibit SOCE without affecting other cellular processes. This contribution documents representative examples of the small-molecule inhibitors of SOCE that have been reported to date. Where possible, methods that were used to characterize the mechanism of action of the inhibitors are also described.
细胞内钙浓度的受控变化是淋巴细胞免疫反应信号通路的关键组成部分。这些细胞中的储存性钙内流(SOCE)会使细胞质Ca(2+)浓度持续升高,并最终导致促炎细胞因子的产生。因此,抑制SOCE的分子可能是治疗类风湿性关节炎、银屑病、炎症性肠病和其他病症的有用免疫调节药物。尽管淋巴细胞和参与免疫反应的其他细胞中存在SOCE信号通路已为人所知多年,但参与SOCE的关键蛋白直到最近才被鉴定出来。这些蛋白的鉴定可能进一步有助于鉴定出在不影响其他细胞过程的情况下抑制SOCE的药物。本论文记录了迄今为止已报道的SOCE小分子抑制剂的代表性实例。在可能的情况下,还描述了用于表征抑制剂作用机制的方法。