Ceroid/lipofuscin-loaded human fibroblasts show decreased survival time and diminished autophagocytosis during amino acid starvation

被引:87
作者
Terman, A [1 ]
Dalen, H
Brunk, UT
机构
[1] Linkoping Univ, Fac Hlth Sci, Dept Neurosci & Locomot, Div Pathol 2, S-58185 Linkoping, Sweden
[2] Inst Gerontol AMS Ukraine, UA-254114 Kiev, Ukraine
[3] Univ Bergen, Gade Inst, Dept Pathol, N-5021 Bergen, Norway
关键词
aging; autophagocytosis; fibroblasts; lipofuscin; lysosomal degradation; starvation;
D O I
10.1016/S0531-5565(99)00070-4
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
To test whether heavy accumulation of ceroid/lipofuscin can disturb important functions of the lysosomal system, AG-1518 human fibroblasts, ceroid/lipofuscin-loaded (following prolonged culture at normobaric hyperoxia) or not, were exposed to amino acid starvation. Ceroid/lipofuscin-loading resulted in decreased cellular survival. Also, there was an inverse relationship between amounts of ceroid/lipofuscin and the survival time of individual cells within the same cultures. Ceroid/lipofusein-loaded fibroblasts displayed diminished autophagocytotic capacity, as demonstrated by electron microscopy and by treatment of cell cultures with NH,CI (which inhibits autophagocytotic degradation by increasing intralysosomal pH) for 1 week before ensuing starvation. The latter treatment increased survival of control cells (due to deposition of nondegraded autophagocytosed material before start of starvation), but not that of ceroid/lipofuscin-loaded cells. Moreover, when NH4Cl treatment was combined with starvation, both groups of cells showed approximately the same shortened survival times, testifying to the causal relationship between diminished autophagocytosis and decreased survival of starving ceroid/lipofuscin-loaded cells. We hypothesize that large amounts of undegradable ceroid/lipofuscin within the acidic vacuolar compartment may interfere with lysosomal function, resulting in poor renewal of long-lived proteins and worn-out/damaged organelles, decreased adaptability, and cell death. (C) 1999 Elsevier Science Inc. All right reserved.
引用
收藏
页码:943 / 957
页数:15
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