Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin

Yuexia Wang, Andrey A. Panteleyev, David M. Owens, Karima Djabali, Colin L. Stewart, Howard J. Worman

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    36 Citations (Scopus)

    Abstract

    Hutchinson-Gilford progeria syndrome (HGPS) is an accelerated aging disorder caused by point mutation in LMNA encoding A-type nuclear lamins. The mutations in LMNA activate a cryptic splice donor site, resulting in expression of a truncated, prenylated prelamin A called progerin. Expression of progerin leads to alterations in nuclear morphology, which may underlie pathology in HGPS. We generated transgenic mice expressing progerin in epidermis under control of a keratin 14 promoter. The mice had severe abnormalities in morphology of skin keratinocyte nuclei, including nuclear envelope lobulation and decreased nuclear circularity not present in transgenic mice expressing wild-type human lamin A. Primary keratinocytes isolated from these mice had a higher frequency of nuclei with abnormal shape compared to those from transgenic mice expressing wild-type human lamin A. Treatment with a farnesyltransferase inhibitor significantly improved nuclear shape abnormalities and induced the formation of intranuclear foci in the primary keratinocytes expressing progerin. Similarly, spontaneous immortalization of progerin-expressing cultured keratinocytes selected for cells with normal nuclear morphology. Despite morphological alterations in keratinocyte nuclei, mice expressing progerin in epidermis had normal hair grown and wound healing. Hair and skin thickness were normal even after crossing to Lmna null mice to reduce or eliminate expression of normal A-type lamins. Although progerin induces significant alterations in keratinocyte nuclear morphology that are reversed by inhibition of farnesyltransferasae, epidermal expression does not lead to alopecia or other skin abnormalities typically seen in human subjects with HGPS.

    Original languageEnglish
    Pages (from-to)2357-2369
    Number of pages13
    JournalHuman Molecular Genetics
    Volume17
    Issue number15
    DOIs
    Publication statusPublished - 1 Aug 2008

    Keywords

    • DREIFUSS MUSCULAR-DYSTROPHY
    • MUTANT LAMIN-A
    • INTERMEDIATE FILAMENT PROTEINS
    • MOUSE MODEL
    • NUCLEAR-ENVELOPE
    • INHIBITING FARNESYLATION
    • DILATED CARDIOMYOPATHY
    • RESTRICTIVE DERMOPATHY
    • COMPREHENSIVE GUIDE
    • SYNDROME MUTATION

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