Shrimpton Corie N, Smith A Ian, Lew Rebecca A
Baker Medical Research Institute, Melbourne, Australia 8008.
Endocr Rev. 2002 Oct;23(5):647-64. doi: 10.1210/er.2001-0032.
Peptidases play a vital and often highly specific role in the physiological and pathological generation and termination of peptide hormone signals. The thermolysin-like family of metalloendopeptidases involved in the extracellular processing of neuroendocrine and cardiovascular peptides are of particular significance, reflecting both their specificity for particular peptide substrates and their utility as therapeutic targets. Although the functions of the membrane-bound members of this family, such as angiotensin-converting enzyme and neutral endopeptidase, are well established, a role for the predominantly soluble family members in peptide metabolism is only just emerging. This review will focus on the biochemistry, cell biology, and physiology of the soluble metalloendopeptidases EC 3.4.24.15 (thimet oligopeptidase) and EC 3.4.24.16 (neurolysin), as well as presenting evidence that both peptidases play an important role in such diverse functions as reproduction, nociception, and cardiovascular homeostasis.
肽酶在肽类激素信号的生理和病理生成及终止过程中发挥着至关重要且往往高度特异的作用。参与神经内分泌和心血管肽细胞外加工的金属内肽酶嗜热菌蛋白酶样家族具有特殊意义,这既体现在它们对特定肽底物的特异性上,也体现在它们作为治疗靶点的实用性上。尽管该家族的膜结合成员(如血管紧张素转换酶和中性内肽酶)的功能已得到充分确立,但主要为可溶性的家族成员在肽代谢中的作用才刚刚显现。本综述将聚焦于可溶性金属内肽酶EC 3.4.24.15(硫醇寡肽酶)和EC 3.4.24.16(神经溶素)的生物化学、细胞生物学和生理学,并提供证据表明这两种肽酶在生殖、伤害感受和心血管稳态等多种功能中发挥着重要作用。