DNase1L2 degrades nuclear DNA during corneocyte formation

被引:56
作者
Fischer, Heinz
Eckhart, Leopold
Mildner, Michael
Jaeger, Karin
Buchberger, Maria
Ghannadan, Minoo
Tschachler, Erwin
机构
[1] Med Univ Vienna, Dept Dermatol, A-1090 Vienna, Austria
[2] Ctr Rech & Invest Epiderm & Sensorielles, Neuilly Sur Seine, France
关键词
D O I
10.1038/sj.jid.5700503
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
The removal of keratinocyte (KC) nuclear DNA by deoxyribonucleases (DNases) is an important step in the formation of normal stratum corneum (SC). However, the molecular identity of the DNA-degrading enzymes has so far remained elusive. Here we show that the endonuclease DNase1-like 2 (DNase1L2) is preferentially expressed in the epidermis and that its expression correlates with terminal differentiation of KC in vitro and in vivo. In biopsies of normal skin, DNase1L2 mRNA was regularly found in suprabasal KC and DNase1L2 protein was highly abundant in the stratum granulosum. In contrast to normal skin, DNase1L2 expression was downregulated in parakeratotic epidermis such as in psoriatic lesions. When DNase1L2 gene expression was knocked down by small interfering RNA in a human skin equivalent model, nuclei were maintained through all layers of the SC. Taken together, our data demonstrate that DNase1L2 plays an essential role in DNA degradation during terminal differentiation of epidermal KC.
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页码:24 / 30
页数:7
相关论文
共 25 条
[1]   The cornified envelope: A model of cell death in the skin [J].
Candi, E ;
Schmidt, R ;
Melino, G .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2005, 6 (04) :328-340
[2]   Terminal differentiation of human keratinocytes and stratum corneum formation is associated with caspase-14 activation [J].
Eckhart, L ;
Declercq, W ;
Ban, J ;
Rendl, M ;
Lengauer, B ;
Mayer, C ;
Lippens, S ;
Vandenabeele, P ;
Tschachler, E .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2000, 115 (06) :1148-1151
[3]   Tumor suppressor NM23-H1 is a granzyme A-activated DNase during CTL-mediated apoptosis, and the nucleosome assembly protein SET is its inhibitor [J].
Fan, ZS ;
Beresford, PJ ;
Oh, DY ;
Zhang, D ;
Lieberman, J .
CELL, 2003, 112 (05) :659-672
[4]   Evidence that apoptosis and terminal differentiation of epidermal keratinocytes are distinct processes [J].
Gandarillas, A ;
Goldsmith, LA ;
Gschmeissner, S ;
Leigh, IM ;
Watt, FM .
EXPERIMENTAL DERMATOLOGY, 1999, 8 (01) :71-79
[5]   IDENTIFICATION OF PROGRAMMED CELL-DEATH INSITU VIA SPECIFIC LABELING OF NUCLEAR-DNA FRAGMENTATION [J].
GAVRIELI, Y ;
SHERMAN, Y ;
BENSASSON, SA .
JOURNAL OF CELL BIOLOGY, 1992, 119 (03) :493-501
[6]  
Haake A, 1999, FITZPATRICKS DERMATO, V5th, P70
[7]  
Holbrook K., 1994, KERATINOCYTE HDB, P3
[8]   Requirement of DNase II for definitive erythropoiesis in the mouse fetal liver [J].
Kawane, K ;
Fukuyama, H ;
Kondoh, G ;
Takeda, J ;
Ohsawa, Y ;
Uchiyama, Y ;
Nagata, S .
SCIENCE, 2001, 292 (5521) :1546-1549
[9]   Deoxyribonuclease IIα is required during the phagocytic phase of apoptosis and its loss causes perinatal lethality [J].
Krieser, RJ ;
MacLea, KS ;
Longnecker, DS ;
Fields, JL ;
Fiering, S ;
Eastman, A .
CELL DEATH AND DIFFERENTIATION, 2002, 9 (09) :956-962
[10]   Differentiation of cultured human epidermal keratinocytes at high cell densities is mediated by endogenous activation of the protein kinase C signaling pathway [J].
Lee, YS ;
Yuspa, SH ;
Dlugosz, AA .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1998, 111 (05) :762-766