Mouse keratin 4 is necessary for internal epithelial integrity

被引:59
作者
Ness, SL
Edelmann, W
Jenkins, TD
Liedtke, W
Rustgi, AK
Kucherlapati, R
机构
[1] Yeshiva Univ Albert Einstein Coll Med, Dept Mol Genet, Bronx, NY 10461 USA
[2] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Hematol Oncol Unit, Boston, MA 02114 USA
[3] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Gastrointestinal Unit, Boston, MA 02114 USA
[4] Yeshiva Univ Albert Einstein Coll Med, Dept Pathol, Div Neuropathol, Bronx, NY 10461 USA
[5] Rockefeller Univ, Howard Hughes Med Inst, New York, NY 10023 USA
关键词
D O I
10.1074/jbc.273.37.23904
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
Keratins are intermediate filaments ts of epithelial cells. Mutations in keratin genes expressed in skis lead to human disorders, including epidermolysis bullosa simplex and epidermolytic hyperkeratosis. We examined the role of keratin 4 (K4) in maintaining the integrity of internal epithelial linings by using gene targeting to generate mice containing a null mutation in the epithelial K4 gene. Homozygous mice that do not express K4 develop a spectrum of phenotypes that affect several organs which express K4 including the esophagus, tongue, and cornea. The cellular phenotypes include basal hyperplasia, Hack of maturation, hyperkeratosis, atypical nuclei, perinuclear clearing, and cell degeneration. These results are consistent with the notion that K4 is required for internal epithelial cell integrity. As mutations in K4 in humans lead to a disorder called white sponge nevus, the K4-deficient mice may serve as models Tor white sponge nevus and for understanding the role of K4 in cellular proliferation and differentiation.
引用
收藏
页码:23904 / 23911
页数:8
相关论文
共 37 条
  • [1] EPIDERMOLYSIS-BULLOSA SIMPLEX - EVIDENCE IN 2 FAMILIES FOR KERATIN GENE ABNORMALITIES
    BONIFAS, JM
    ROTHMAN, AL
    EPSTEIN, EH
    [J]. SCIENCE, 1991, 254 (5035) : 1202 - 1205
  • [2] A HUMAN KERATIN-14 KNOCKOUT - THE ABSENCE OF K14 LEADS TO SEVERE EPIDERMOLYSIS-BULLOSA SIMPLEX AND A FUNCTION FOR AN INTERMEDIATE FILAMENT PROTEIN
    CHAN, YM
    ANTONLAMPRECHT, I
    YU, QC
    JACKEL, A
    ZABEL, B
    ERNST, JP
    FUCHS, E
    [J]. GENES & DEVELOPMENT, 1994, 8 (21) : 2574 - 2587
  • [3] THE GENETIC-BASIS OF EPIDERMOLYTIC HYPERKERATOSIS - A DISORDER OF DIFFERENTIATION-SPECIFIC EPIDERMAL KERATIN GENES
    CHENG, J
    SYDER, AJ
    YU, QC
    LETAI, A
    PALLER, AS
    FUCHS, E
    [J]. CELL, 1992, 70 (05) : 811 - 819
  • [4] A LEUCINE-]PROLINE MUTATION IN THE H1 SUBDOMAIN OF KERATIN-1 CAUSES EPIDERMOLYTIC HYPERKERATOSIS
    CHIPEV, CC
    KORGE, BP
    MARKOVA, N
    BALE, SJ
    DIGIOVANNA, JJ
    COMPTON, JG
    STEINERT, PM
    [J]. CELL, 1992, 70 (05) : 821 - 828
  • [5] COMPTON JG, 1991, ANN NY ACAD SCI, V642, P32
  • [6] POINT MUTATIONS IN HUMAN KERATIN-14 GENES OF EPIDERMOLYSIS-BULLOSA SIMPLEX PATIENTS - GENETIC AND FUNCTIONAL ANALYSES
    COULOMBE, PA
    HUTTON, ME
    LETAI, A
    HEBERT, A
    PALLER, AS
    FUCHS, E
    [J]. CELL, 1991, 66 (06) : 1301 - 1311
  • [7] WHITE SPONGE NEVUS (LEUKOEDEMA EXFOLIATIVUM MUCOSAE ORIS) - ULTRASTRUCTURAL OBSERVATIONS
    FRITHIOF, L
    BANOCZY, J
    [J]. ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY AND ENDODONTICS, 1976, 41 (05): : 607 - 622
  • [8] INTERMEDIATE FILAMENTS - STRUCTURE, DYNAMICS, FUNCTION, AND DISEASE
    FUCHS, E
    WEBER, K
    [J]. ANNUAL REVIEW OF BIOCHEMISTRY, 1994, 63 : 345 - 382
  • [9] MORPHOLOGY, BEHAVIOR, AND INTERACTION OF CULTURED EPITHELIAL-CELLS AFTER THE ANTIBODY-INDUCED DISRUPTION OF KERATIN FILAMENT ORGANIZATION
    KLYMKOWSKY, MW
    MILLER, RH
    LANE, EB
    [J]. JOURNAL OF CELL BIOLOGY, 1983, 96 (02) : 494 - 509
  • [10] NONEPIDERMAL MEMBERS OF THE KERATIN MULTIGENE FAMILY - CDNA SEQUENCES AND INSITU LOCALIZATION OF THE MESSENGER-RNAS
    KNAPP, B
    RENTROP, M
    SCHWEIZER, J
    WINTER, H
    [J]. NUCLEIC ACIDS RESEARCH, 1986, 14 (02) : 751 - 763