Lutgens Suzanne P M, Cleutjens Kitty B J M, Daemen Mat J A P, Heeneman Sylvia
Department of Pathology, Cardiovascular Research Institute Maastricht, Maastricht University, P.O. Box 616, 6200 MD Maastricht, The Netherlands.
FASEB J. 2007 Oct;21(12):3029-41. doi: 10.1096/fj.06-7924com. Epub 2007 May 23.
Extracellular matrix (ECM) remodeling is one of the underlying mechanisms in cardiovascular diseases. Cathepsin cysteine proteases have a central role in ECM remodeling and have been implicated in the development and progression of cardiovascular diseases. Cathepsins also show differential expression in various stages of atherosclerosis, and in vivo knockout studies revealed that deficiency of cathepsin K or S reduces atherosclerosis. Furthermore, cathepsins are involved in lipid metabolism. Cathepsins have the capability to degrade low-density lipoprotein and reduce cholesterol efflux from macrophages, aggravating foam cell formation. Although expression studies also demonstrated differential expression of cathepsins in cardiovascular diseases like aneurysm formation, neointima formation, and neovascularization, in vivo studies to define the exact role of cathepsins in these processes are lacking. Evaluation of the feasibility of cathepsins as a diagnostic tool revealed that serum levels of cathepsins L and S seem to be promising as biomarkers in the diagnosis of atherosclerosis, whereas cathepsin B shows potential as an imaging tool. Furthermore, cathepsin K and S inhibitors showed effectiveness in (pre) clinical evaluation for the treatment of osteoporosis and osteoarthritis, suggesting that cathepsin inhibitors may also have therapeutic effects for the treatment of atherosclerosis.
细胞外基质(ECM)重塑是心血管疾病的潜在机制之一。组织蛋白酶半胱氨酸蛋白酶在ECM重塑中起核心作用,并与心血管疾病的发生和发展有关。组织蛋白酶在动脉粥样硬化的各个阶段也表现出差异表达,体内基因敲除研究表明,组织蛋白酶K或S的缺乏可减轻动脉粥样硬化。此外,组织蛋白酶参与脂质代谢。组织蛋白酶具有降解低密度脂蛋白的能力,并减少巨噬细胞的胆固醇外流,加重泡沫细胞的形成。尽管表达研究也证明了组织蛋白酶在诸如动脉瘤形成、新生内膜形成和新血管形成等心血管疾病中的差异表达,但缺乏体内研究来确定组织蛋白酶在这些过程中的确切作用。对组织蛋白酶作为诊断工具的可行性评估表明,组织蛋白酶L和S的血清水平似乎有望作为动脉粥样硬化诊断的生物标志物,而组织蛋白酶B显示出作为成像工具的潜力。此外,组织蛋白酶K和S抑制剂在骨质疏松症和骨关节炎治疗的(前)临床评估中显示出有效性,这表明组织蛋白酶抑制剂可能对动脉粥样硬化的治疗也有治疗作用。