Extracellular Matrix Pathology Section, Laboratory of Pathology, National Cancer Institute, National Institute of Health, Bethesda, MD, United States.
Extracellular Matrix Pathology Section, Laboratory of Pathology, National Cancer Institute, National Institute of Health, Bethesda, MD, United States; Department of Orthopedics, Washington University in St. Louis School of Medicine, United States.
Matrix Biol. 2023 Nov;123:59-70. doi: 10.1016/j.matbio.2023.09.002. Epub 2023 Oct 6.
Extracellular proteolysis and turnover are core processes of tissue homeostasis. The predominant matrix-degrading enzymes are members of the Matrix Metalloproteinase (MMP) family. MMPs extensively degrade core matrix components in addition to processing a range of other factors in the extracellular, plasma membrane, and intracellular compartments. The proteolytic activity of MMPs is modulated by the Tissue Inhibitors of Metalloproteinases (TIMPs), a family of four multi-functional matrisome proteins with extensively characterized MMP inhibitory functions. Thus, a well-regulated balance between MMP activity and TIMP levels has been described as critical for healthy tissue homeostasis, and this balance can be chronically disturbed in pathological processes. The relationship between MMPs and TIMPs is complex and lacks the constraints of a typical enzyme-inhibitor relationship due to secondary interactions between various MMPs (specifically gelatinases) and TIMP family members. We illustrate a new complexity in this system by describing how MMP9 can cleave members of the TIMP family when in molar excess. Proteolytic processing of TIMPs can generate functionally altered peptides with potentially novel attributes. We demonstrate here that all TIMPs are cleaved at their C-terminal tails by a molar excess of MMP9. This processing removes the N-glycosylation site for TIMP3 and prevents the TIMP2 interaction with latent proMMP2, a prerequisite for cell surface MMP14-mediated activation of proMMP2. TIMP2/4 are further cleaved producing ∼14 kDa N-terminal proteins linked to a smaller C-terminal domain through residual disulfide bridges. These cleaved TIMP2/4 complexes show perturbed MMP inhibitory activity, illustrating that MMP9 may bear a particularly prominent influence upon the TIMP:MMP balance in tissues.
细胞外蛋白水解和周转是组织稳态的核心过程。主要的基质降解酶是基质金属蛋白酶 (MMP) 家族的成员。MMP 广泛降解核心基质成分,除了处理细胞外、质膜和细胞内隔室中的一系列其他因子。MMP 的蛋白水解活性受基质金属蛋白酶抑制剂 (TIMP) 调节,TIMP 是一个具有广泛特征的 MMP 抑制功能的多功能基质体蛋白家族。因此,MMP 活性和 TIMP 水平之间的良好调节平衡被描述为健康组织稳态的关键,这种平衡在病理过程中可能会长期受到干扰。MMP 和 TIMP 之间的关系很复杂,由于各种 MMP(特别是明胶酶)和 TIMP 家族成员之间的二次相互作用,缺乏典型的酶抑制剂关系的限制。我们通过描述 MMP9 如何在摩尔过量时切割 TIMP 家族成员来阐明该系统的新复杂性。TIMP 的蛋白水解加工可以产生具有潜在新特性的功能改变的肽。我们在这里证明,所有 TIMP 都被摩尔过量的 MMP9 在其 C 端尾部切割。这种处理去除了 TIMP3 的 N-糖基化位点,并阻止了 TIMP2 与潜伏的 proMMP2 的相互作用,这是细胞表面 MMP14 介导的 proMMP2 激活的先决条件。TIMP2/4 进一步切割产生约 14 kDa 的 N 端蛋白,通过残留的二硫键与较小的 C 端结构域相连。这些切割的 TIMP2/4 复合物显示出 MMP 抑制活性受损,表明 MMP9 可能对组织中 TIMP:MMP 平衡具有特别突出的影响。