Ceroid/lipofuscin-loaded human fibroblasts show increased susceptibility to oxidative stress

被引:70
作者
Terman, A [1 ]
Abrahamsson, N
Brunk, UT
机构
[1] Linkoping Univ, Fac Hlth Sci, Div Pathol 2, S-58185 Linkoping, Sweden
[2] Ukraine Acad Med Sci, Inst Gerontol, UA-254114 Kiev, Ukraine
关键词
aging; cell death; fibroblasts; lipofuscin; lysosomes; oxidative stress;
D O I
10.1016/S0531-5565(99)00045-5
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 the possibly enhanced sensitivity of aged cells to oxidative stress may depend on their content of ceroid/lipofuscin, AG-1518 human fibroblasts with various amounts of the pigment accumulated due to prolonged cultivation under normobaric hyperoxia were exposed to acute oxidative stress (2.5 mu M naphthazarin, 15 min) and then returned to standard culture conditions. Twenty-four hours after the naphthazarin treatment, 37% of the cells were still vital, whereas others had undergone oxidative stress-induced apoptosis with ensuing postapoptotic necrosis. The average amount of ceroid/lipofuscin within the surviving cells was only about half of that of the initial population of cells, as measured before the naphthazarin exposure. This finding suggests that ceroid/lipofuscin-rich cells have an increased sensitivity to oxidative stress. The ceroid/lipofuscin quantity strongly positively correlated with the size of the acidic compartment (as evaluated by uptake of the weakly basic lysosomotropic fluorochrome acridine orange) and with its content of the lysosomal protease cathepsin D, as assayed by immunocytochemistry. We hypothesize that the enhanced sensitivity of ceroid/lipofuscin-loaded cells to oxidative: stress may be caused by the increased amounts of lysosomal enzymes, known as mediators of oxidative damage, and/or by catalysis of intralysosomal oxidative reactions by lipofuscin-associated iron. (C) 1999 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:755 / 770
页数:16
相关论文
共 59 条
[1]  
Armstrong D, 1981, AGE PIGMENTS, P355
[2]   HUMAN-SKIN FIBROBLASTS INVITRO DIFFERENTIATE ALONG A TERMINAL CELL LINEAGE [J].
BAYREUTHER, K ;
RODEMANN, HP ;
HOMMEL, R ;
DITTMANN, K ;
ALBIEZ, M ;
FRANCZ, PI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (14) :5112-5116
[3]   ULTRASTRUCTURAL AND CYTOCHEMICAL CHANGES IN CULTURED HUMAN LUNG CELLS [J].
BRANDES, D ;
ANTON, EB ;
BARNARD, S ;
MURPHY, DG .
JOURNAL OF ULTRASTRUCTURE RESEARCH, 1972, 39 (5-6) :465-&
[4]   COMPARATIVE ULTRASTRUCTURE OF CHICK FIBROBLASTS IN-VITRO AT EARLY AND LATE STAGES DURING THEIR GROWTH SPAN [J].
BROCK, MA ;
HAY, RJ .
JOURNAL OF ULTRASTRUCTURE RESEARCH, 1971, 36 (3-4) :291-+
[5]   HISTOCHEMICAL INDICATIONS FOR LYSOSOMAL LOCALIZATION OF HEAVY METALS IN NORMAL RAT BRAIN AND LIVER [J].
BRUN, A ;
BRUNK, U .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1970, 18 (11) :820-&
[6]   RESIDUAL BODIES AND AGING IN CULTURED HUMAN GLIA CELLS - EFFECT OF ENTRANCE INTO PHASE III AND PROLONGED PERIODS OF CONFLUENCE [J].
BRUNK, U ;
ERICSSON, JL ;
PONTEN, J ;
WESTERMARK, B .
EXPERIMENTAL CELL RESEARCH, 1973, 79 (01) :1-14
[7]   Oxidative stress, growth factor starvation and Fas activation may all cause apoptosis through lysosomal leak [J].
Brunk, UT ;
Svensson, I .
REDOX REPORT, 1999, 4 (1-2) :3-11
[8]   EXPOSURE OF CELLS TO NONLETHAL CONCENTRATIONS OF HYDROGEN-PEROXIDE INDUCES DEGENERATION-REPAIR MECHANISMS INVOLVING LYSOSOMAL DESTABILIZATION [J].
BRUNK, UT ;
ZHANG, H ;
DALEN, H ;
OLLINGER, K .
FREE RADICAL BIOLOGY AND MEDICINE, 1995, 19 (06) :813-822
[9]   LETHAL HYDROGEN-PEROXIDE TOXICITY INVOLVES LYSOSOMAL IRON-CATALYZED REACTIONS WITH MEMBRANE DAMAGE [J].
BRUNK, UT ;
ZHANG, H ;
ROBERG, K ;
OLLINGER, K .
REDOX REPORT, 1995, 1 (04) :267-277
[10]   A NOVEL HYPOTHESIS OF LIPOFUSCINOGENESIS AND CELLULAR AGING BASED ON INTERACTIONS BETWEEN OXIDATIVE STRESS AND AUTOPHAGOCYTOSIS [J].
BRUNK, UT ;
JONES, CB ;
SOHAL, RS .
MUTATION RESEARCH, 1992, 275 (3-6) :395-403