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Delayed wound healing in keratin 6a knockout mice
Author(s): Wojcik SM, Bundman DS, Roop DR
Source: MOLECULAR AND CELLULAR BIOLOGY    Volume: 20    Issue: 14    Pages: 5248-5255    Published: JUL 2000  
Times Cited: 63     References: 47     
Abstract: Keratin 6 (K6) expression in the epidermis has two components: constitutive expression in the innermost layer of the outer root sheath (ORS) of hair follicles and inducible expression in the interfollicular epidermis in response to stressful stimuli such as wounding. Mice express two K6 isoforms, MK6a and MK6b. To gain insight into the functional significance of these isoforms, we generated MK6a-deficient mice through mouse embryonic stem cell technology. Upon wounding, MK6a was induced in the outer ORS and the interfollicular epidermis including the basal cell layer of MK6a(+/+) mice, whereas MK6b induction in MK6a(-/-) mice was restricted to the suprabasal layers of the epidermis. After superficial mounding of the epidermis by tape stripping, MK6a(-/-) mice showed a delay in reepithelialization from the hair follicle. However, the healing of full-thickness skin wounds was not impaired in MK6a(-/-) animals. Migration and proliferation of MK6a(-/-) keratinocytes were not impaired in vitro. Furthermore, the migrating and the proliferating keratinocytes of full-thickness wounds in MK6a(-/-) animals expressed neither MK6a nor MK6b. These data indicate that MK6a does not play a major role in keratinocyte proliferation or migration but point to a role in the activation of follicular keratinocytes after wounding. This study represents the first report of a keratin null mutation that results in a wound healing defect.
Document Type: Article
Language: English
Reprint Address: Roop, DR (reprint author), Baylor Coll Med, Dept Mol & Cellular Biol, 1 Baylor Plaza, Houston, TX 77030 USA
Addresses:
1. Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
2. Baylor Coll Med, Dept Dermatol, Houston, TX 77030 USA
Publisher: AMER SOC MICROBIOLOGY, 1752 N ST NW, WASHINGTON, DC 20036-2904 USA
Subject Category: Biochemistry & Molecular Biology; Cell Biology
IDS Number: 327XP
ISSN: 0270-7306
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