Davies P, Allison A C
Front Biol. 1976;45:61-98.
The studies reviewed in this chapter provide further evidence that the secretion of lysosomal enzymes and other hydrolases is a constitutive function of certain cells whereas in other cells is an inducible process probably contributing to the pathology of a variety of diseases. Little is known of the mechanisms mediating the secretion of lysosomal enzymes. We have summarized evidence suggesting a role of microfilaments and microtubules in controlling enzyme release, but further studies of the biochemical mechanisms which control the activity of these subcellular structures are required. The fusion of lysosomes with the plasma membrane has been observed in several situations and the mechanisms underlying processes of this nature have been studied in lower organisms (Satir et al. 1973; Plattner 1974). Agents, such as concanavalin A, which interfere with the fusion of endosomes with lysosomes (Goldman 1974; Edelson and Cohn 1974a, b) should also be useful in determining the chemical nature of membrane components involved in the fusion process. New information on the fate of secreted acid hydrolases has been obtained from studies of the uptake of lysosomal enzymes by fibroblasts. Clearly, the mechanisms by which these cells endocytose secreted lysosomal enzymes will be a subject for detailed study in view of the important of directing enzymes and drugs into lysosomes (De Duve et al. 1974). The mechanisms by which extracellular inhibitors inactivate hydrolytic enzymes, particularly proteinases, is also being clarified (for review see Davies 1975) and this should aid in finding new ways for preventing tissue damage caused by the excessive secretion of these enzymes. Further investigation concerning the secretion of lysosomal enzymes should establish the essential physiological role which these enzymes play at both extracellular and intracellular sites. Also, a close examination of the interaction of both endogenous and exogenous stimuli of inflammation with cells resulting in the secretion of hydrolytic enzymes, will clarify the mechanisms underlying the initiation and progression of the inflammatory process in its diverse forms.
本章中所综述的研究进一步证明,溶酶体酶和其他水解酶的分泌是某些细胞的组成性功能,而在其他细胞中则是一个诱导过程,可能与多种疾病的病理过程有关。关于介导溶酶体酶分泌的机制,人们了解甚少。我们总结了一些证据,表明微丝和微管在控制酶释放方面发挥作用,但还需要对控制这些亚细胞结构活性的生化机制进行进一步研究。在几种情况下都观察到了溶酶体与质膜的融合,并且在低等生物中对这种性质的过程的潜在机制进行了研究(萨蒂尔等人,1973年;普拉特纳,1974年)。诸如伴刀豆球蛋白A等干扰内体与溶酶体融合的试剂(戈德曼,1974年;埃德尔森和科恩,1974年a、b)也应有助于确定参与融合过程的膜成分的化学性质。关于分泌的酸性水解酶命运的新信息已从成纤维细胞对溶酶体酶摄取的研究中获得。显然,鉴于将酶和药物导向溶酶体的重要性(德·迪夫等人,1974年),这些细胞内吞分泌的溶酶体酶的机制将成为详细研究的课题。细胞外抑制剂使水解酶特别是蛋白酶失活的机制也正在得到阐明(综述见戴维斯,1975年),这应该有助于找到防止这些酶过度分泌所导致的组织损伤的新方法。关于溶酶体酶分泌的进一步研究应该确定这些酶在细胞外和细胞内位点所发挥的基本生理作用。此外,仔细研究炎症的内源性和外源性刺激与导致水解酶分泌的细胞之间的相互作用,将阐明炎症过程以其多种形式发生起始和进展的潜在机制。