Expression of the anti-apoptotic protein Hsp27 during both the keratinocyte differentiation and dedifferentiation of HaCat cells: expression linked to changes in intracellular protein organization?

被引:19
作者
Arrigo, AP [1 ]
Ducasse, U [1 ]
机构
[1] Univ Lyon 1, CNRS UMR 5534, Equipe Stress Oxydant Chaperons & Apoptose, F-69622 Villeurbanne, France
关键词
Hsp27; keratinocyte; differentiation; oligomerization; aging;
D O I
10.1016/S0531-5565(02)00131-6
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
We show here that Hsp27 increases its level of expression during the late phase of the keratinocyte differentiation of human HaCat cells. A similar phenomenon was observed when differentiated HaCat cells underwent a dedifferentiation. process. In both cases, Hsp27 accumulated in the form of large native structures, which represent the chaperone active form of the protein. Hence, the presence of Hsp27 large oligomers does not appear to be the consequence of a particular differentiation process but should be considered as a marker of endogenous stress conditions. Such conditions may arise when drastic changes in the intracellular protein organization occur, such as during differentiation, dedifferentiation and probably also during the development of the senescent phenotype. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:1247 / 1255
页数:9
相关论文
共 41 条
[31]   Comparison of the protective activities generated by two survival proteins: Bcl-2 and Hsp27 in L929 murine fibroblasts exposed to menadione or staurosporine [J].
Paul, C ;
Arrigo, AP .
EXPERIMENTAL GERONTOLOGY, 2000, 35 (6-7) :757-766
[32]   OXIDANTS AND ANTIOXIDANTS IN PROLIFERATIVE SENESCENCE [J].
POOT, M .
MUTATION RESEARCH, 1991, 256 (2-6) :177-189
[33]   Mammalian small stress proteins protect against oxidative stress through their ability to increase glucose-6-phosphate dehydrogenase activity and by maintaining optimal cellular detoxifying machinery [J].
Préville, X ;
Salvemini, F ;
Giraud, S ;
Chaufour, S ;
Paul, C ;
Stepien, G ;
Ursini, MV ;
Arrigo, AP .
EXPERIMENTAL CELL RESEARCH, 1999, 247 (01) :61-78
[34]   Regulation of Hsp27 oligomerization, chaperone function, and protective activity against oxidative stress tumor necrosis factor α by phosphorylation [J].
Rogalla, T ;
Ehrnsperger, M ;
Preville, X ;
Kotlyarov, A ;
Lutsch, G ;
Ducasse, C ;
Paul, C ;
Wieske, M ;
Arrigo, AP ;
Buchner, J ;
Gaestel, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (27) :18947-18956
[35]   EXPRESSION OF HEAT-SHOCK GENES DURING DIFFERENTIATION OF MAMMALIAN OSTEOBLASTS AND PROMYELOCYTIC LEUKEMIA-CELLS [J].
SHAKOORI, AR ;
OBERDORF, AM ;
OWEN, TA ;
WEBER, LA ;
HICKEY, E ;
STEIN, JL ;
LIAN, JB ;
STEIN, GS .
JOURNAL OF CELLULAR BIOCHEMISTRY, 1992, 48 (03) :277-287
[36]   REGULATION OF THE 28 KDA HEAT-SHOCK PROTEIN BY RETINOIC ACID DURING DIFFERENTIATION OF HUMAN LEUKEMIC HL-60 CELLS [J].
SPECTOR, NL ;
MEHLEN, P ;
RYAN, C ;
HARDY, L ;
SAMSON, W ;
LEVINE, H ;
NADLER, LM ;
FABRE, N ;
ARRIGO, AP .
FEBS LETTERS, 1994, 337 (02) :184-188
[37]   HEAT-SHOCK PROTEIN IS A UNIQUE MARKER OF GROWTH ARREST DURING MACROPHAGE DIFFERENTIATION OF HL-60 CELLS [J].
SPECTOR, NL ;
RYAN, C ;
SAMSON, W ;
LEVINE, H ;
NADLER, LM ;
ARRIGO, AP .
JOURNAL OF CELLULAR PHYSIOLOGY, 1993, 156 (03) :619-625
[38]  
SPECTOR NL, 1992, J IMMUNOL, V148, P1668
[39]   THE SMALL HEAT-SHOCK PROTEIN HSP25 IS ACCUMULATED IN P19 EMBRYONAL CARCINOMA-CELLS AND EMBRYONIC STEM-CELLS OF LINE BLC6 DURING DIFFERENTIATION [J].
STAHL, J ;
WOBUS, AM ;
IHRIG, S ;
LUTSCH, G ;
BIELKA, H .
DIFFERENTIATION, 1992, 51 (01) :33-37
[40]   DIFFERENCES IN EFFECTS OF ONCOGENES ON RESISTANCE TO GAMMA-RAYS, ULTRAVIOLET-LIGHT, AND HEAT-SHOCK [J].
SUZUKI, K ;
WATANABE, M ;
MIYOSHI, J .
RADIATION RESEARCH, 1992, 129 (02) :157-162