NORMAL PSORIATIC EPIDERMIS EXPRESSION OF HYPERPROLIFERATION-ASSOCIATED KERATINS

被引:102
作者
THEWES, M
STADLER, R
KORGE, B
MISCHKE, D
机构
[1] MED CTR MINDEN, DEPT DERMATOL, PORTASTR 7-9, W-4950 MINDEN, GERMANY
[2] FREE UNIV BERLIN, W-1000 BERLIN 33, GERMANY
[3] NIAMSD, DEPT DERMATOL, SKIN BIOL LAB, BETHESDA, MD USA
[4] UNIV CTR CHARLOTTENBURG, INST EXPTL ONCOL & TRANSPLANTAT, BERLIN, GERMANY
关键词
PSORIASIS; KERATIN EXPRESSION; HYPERPROLIFERATION; KOBNER EFFECT;
D O I
10.1007/BF00371784
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Keratin expression in lesional, marginal and uninvolved psoriatic epidermis was analysed by one- and two-dimensional gel electrophoresis and immunoblotting. Keratins K1, K5, K6, K1O, K14, and K16 were identified in lesional epidermis. Keratins K6 and K16 were found in all epidermis probes of uninvolved skin, but never occurred in normal epidermis of control skin samples. By means of laser-densitometric evaluation of one-dimensional gels a downregulation of K1 and K1O and an upregulation of K6 and K16 was found in psoriatic epidermis. Unexpectedly, the level of K5 was considerably lower and the level of K14 considerably higher in lesional skin than in normal epidermis. These results demonstrate that not only basal keratinocytes in lesional epidermis but also suprabasal keratinocytes in uninvolved psoriatic epidermis express an altered differentiation pattern. The latter phenomenon could be very important in understanding the development of the so-called "Kobner effect" in psoriatic epidermis.
引用
收藏
页码:465 / 471
页数:7
相关论文
共 42 条
[1]   KERATIN POLYPEPTIDES OF PSORIATIC EPIDERMIS [J].
BADEN, HP ;
MCGILVRAY, N ;
CHENG, CK ;
LEE, LD ;
KUBILUS, J .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1978, 70 (05) :294-297
[2]  
COOPER D, 1986, J BIOL CHEM, V261, P4646
[3]  
DEMARE S, 1990, BRIT J DERMATOL, V122, P469
[4]   EPIDERMAL HYPERPROLIFERATION ASSESSED BY THE MONOCLONAL-ANTIBODY KS8.12 ON FROZEN-SECTIONS [J].
DEMARE, S ;
VANERP, PEJ ;
VANDEKERKHOF, PCM .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1989, 92 (01) :130-131
[5]   CLONING OF CDNAS SPECIFYING VITAMIN-A-RESPONSIVE HUMAN KERATINS [J].
ECKERT, RL ;
GREEN, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (14) :4321-4325
[6]   CLASSIFICATION OF EPIDERMAL KERATINS ACCORDING TO THEIR IMMUNOREACTIVITY, ISOELECTRIC POINT, AND MODE OF EXPRESSION [J].
EICHNER, R ;
BONITZ, P ;
SUN, TT .
JOURNAL OF CELL BIOLOGY, 1984, 98 (04) :1388-1396
[7]   THE ROLE OF KERATIN SUBFAMILIES AND KERATIN PAIRS IN THE FORMATION OF HUMAN EPIDERMAL INTERMEDIATE FILAMENTS [J].
EICHNER, R ;
SUN, TT ;
AEBI, U .
JOURNAL OF CELL BIOLOGY, 1986, 102 (05) :1767-1777
[8]   TYPE-I AND TYPE-II KERATINS HAVE EVOLVED FROM LOWER EUKARYOTES TO FORM THE EPIDERMAL INTERMEDIATE FILAMENTS IN MAMMALIAN SKIN [J].
FUCHS, E ;
MARCHUK, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (19) :5857-5861
[9]   CHANGES IN KERATIN GENE-EXPRESSION DURING TERMINAL DIFFERENTIATION OF THE KERATINOCYTE [J].
FUCHS, E ;
GREEN, H .
CELL, 1980, 19 (04) :1033-1042
[10]  
FUCHS E, 1981, CELL, V25, P617, DOI 10.1016/0092-8674(81)90169-0