Molloy Eamonn S, McCarthy Geraldine M
Department of Clinical Pharmacology, Royal College of Surgeons in Ireland, 123 St. Stephen's Green, Dublin 2, Ireland.
Curr Rheumatol Rep. 2004 Jun;6(3):228-34. doi: 10.1007/s11926-004-0073-5.
Basic calcium phosphate, calcium pyrophosphate dihydrate, and monosodium urate crystals are the most common types of crystals associated with human disease. Although there is a well-established association between these crystals and various forms of joint disease, recent evidence points to an association of basic calcium phosphate crystals with breast cancer and atherosclerosis. Crystal-induced tissue damage is affected by degradative proteases, cytokines, chemokines, and prostanoids produced by cells stimulated by crystals. In the case of basic calcium phosphate and calcium pyrophosphate dihydrate crystals, these responses are augmented by the cellular proliferation that results from their induction of mitogenesis. The understanding of the molecular mechanisms involved in generating these pathologic effects has been significantly advanced in recent years. Such advances are essential to the ongoing search for more effective therapies for crystal-associated diseases.
碱性磷酸钙、二水焦磷酸钙和尿酸钠晶体是与人类疾病相关的最常见晶体类型。尽管这些晶体与各种形式的关节疾病之间存在已确立的关联,但最近的证据表明碱性磷酸钙晶体与乳腺癌和动脉粥样硬化有关。晶体诱导的组织损伤受晶体刺激的细胞产生的降解蛋白酶、细胞因子、趋化因子和类前列腺素的影响。就碱性磷酸钙和二水焦磷酸钙晶体而言,这些反应因它们诱导有丝分裂而导致的细胞增殖而增强。近年来,对产生这些病理效应所涉及的分子机制的理解有了显著进展。这些进展对于正在进行的寻找更有效治疗晶体相关疾病的疗法至关重要。