Epidermal differentiation does not involve the pro-apoptotic executioner caspases, but is associated with caspase-14 induction and processing

被引:209
作者
Lippens, S
Kockx, M
Knaapen, M
Mortier, L
Polakowska, R
Verheyen, A
Garmyn, M
Zwijsen, A
Formstecher, P
Huylebroeck, D
Vandenabeele, P
Declercq, W
机构
[1] Flanders Interuniv, Inst Biotechnol, Dept Mol Biol, Mol Signaling & Cell Death Unit, B-9000 Ghent, Belgium
[2] State Univ Ghent, B-9000 Ghent, Belgium
[3] Univ Hosp Middelheim, APCAM & Dermatol, Dept Pathol, B-2020 Antwerp, Belgium
[4] Fac Med Henri Warembourg, INSERM, U459, F-59045 Lille, France
[5] Catholic Univ Louvain, Dept Dermatol, B-3000 Louvain, Belgium
[6] Flanders Interuniv, Inst Biotechnol, Mol Biol Lab, Dept Cell Growth Differentiat & Dev, B-3000 Louvain, Belgium
关键词
caspase; skin; keratinocyte; differentiation; psoriasis;
D O I
10.1038/sj.cdd.4400785
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The epidermis is a stratified squamous epithelium in which keratinocytes progressively undergo terminal differentiation towards the skin surface leading to programmed cell death. In this respect we studied the role of caspases. Here, we show that caspase-14 synthesis in the skin is restricted to differentiating keratinocytes and that caspase-14 processing is associated with terminal epidermal differentiation, The pro-apoptotic executioner caspases-3, -6, and -7 are not activated during epidermal differentiation. Caspase-14 does not participate in apoptotic pathways elicited by treatment of differentiated keratinocytes with various death-inducing stimuli, in contrast to caspase-3. In addition, we show that non-cornifying oral keratinocyte epithelium does not express caspase-14 and that the parakeratotic regions of psoriatic skin lesions contain very low levels of caspase-14 as compared to normal stratum corneum. These observations strongly suggest that caspase-14 is involved in the keratinocyte terminal differentiation program leading to normal skin cornification, while the executioner caspases are not implicated.
引用
收藏
页码:1218 / 1224
页数:7
相关论文
共 38 条
  • [11] HAAKE AR, 1995, CELL DEATH DIFFER, V2, P183
  • [12] THE SECRET LIFE OF THE HAIR FOLLICLE
    HARDY, MH
    [J]. TRENDS IN GENETICS, 1992, 8 (02) : 55 - 61
  • [13] The genetics of psoriasis
    Henseler, T
    [J]. JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1997, 37 (02) : S1 - S11
  • [14] Holbrook K.A., 1983, BIOCH PHYSL SKIN, V1, P64
  • [15] Caspase-14 is a novel developmentally regulated protease
    Hu, SM
    Snipas, SJ
    Vincenz, C
    Salvesen, G
    Dixit, VM
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (45) : 29648 - 29653
  • [16] SEPARATION OF THE EPIDERMAL SHEET BY DISPASE
    KITANO, Y
    OKADA, N
    [J]. BRITISH JOURNAL OF DERMATOLOGY, 1983, 108 (05) : 555 - 560
  • [17] CLEAVAGE OF POLY(ADP-RIBOSE) POLYMERASE BY A PROTEINASE WITH PROPERTIES LIKE ICE
    LAZEBNIK, YA
    KAUFMANN, SH
    DESNOYERS, S
    POIRIER, GG
    EARNSHAW, WC
    [J]. NATURE, 1994, 371 (6495) : 346 - 347
  • [18] Cytochrome c and dATP-dependent formation of Apaf-1/caspase-9 complex initiates an apoptotic protease cascade
    Li, P
    Nijhawan, D
    Budihardjo, I
    Srinivasula, SM
    Ahmad, M
    Alnemri, ES
    Wang, XD
    [J]. CELL, 1997, 91 (04) : 479 - 489
  • [19] Activation of caspase-1 in the nucleus requires nuclear translocation of pro-caspase-1 mediated by its prodomain
    Mao, PL
    Jiang, YL
    Wee, BY
    Porter, AG
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (37) : 23621 - 23624
  • [20] Comparison of caspase activation and subcellular localization in HL-60 and K562 cells undergoing etoposide-induced apoptosis
    Martins, LM
    Mesner, PW
    Kottke, TJ
    Basi, GS
    Sinha, S
    Tung, JS
    Svingen, PA
    Madden, BJ
    Takahashi, A
    McCormick, DJ
    Earnshaw, WC
    Kaufmann, SH
    [J]. BLOOD, 1997, 90 (11) : 4283 - 4296