Literature DB >> 7688400

Antisense profilaggrin RNA delays and decreases profilaggrin expression and alters in vitro differentiation of rat epidermal keratinocytes.

P V Haydock1, C Blomquist, S Brumbaugh, B A Dale, K A Holbrook, P Fleckman.   

Abstract

Ichthyosis vulgaris is an epidermal disorder in which profilaggrin expression is decreased or absent. To determine whether the ichthyosis vulgaris phenotype could be mimicked by eliminating profilaggrin expression, a rat epidermal cell line was transfected with a plasmid that directs the constitutive expression of an RNA that is antisense to normal profilaggrin mRNA. Non-transfected and neomycin-resistant cells not containing antisense plasmid that were grown in the neomycin analogue G418 served as controls. Immunoblot and immunofluorescence analysis showed that profilaggrin protein expression and processing to filaggrin were delayed by 3 to 4 d and decreased in transfected cells. Profilaggrin mRNA was detected in both control and transfected cells only after the cells reached confluence, whereas antisense RNA was detected in transfectants at all times, even prior to confluence. Ultrastructural examination revealed that keratohyalin granules were decreased in number, globular, and heterogeneous in appearance in transfected cells in-contrast to angular structures seen in control cells. Unexpectedly, stratification was impaired, intermediate filaments were noticeably reduced, and cornified cell envelope formation was delayed in transfectants. Unlike ichthyosis vulgaris keratinocytes, where keratin expression is unaffected, appearance of K1 and K10 was delayed and K1/K10 synthesis was delayed and decreased in transfected cells. The precipitous drop in 35S-methionine incorporation into cytoskeletal protein seen at confluence in control cells was delayed by 3 d in transfected cells. We conclude that, rather than producing the ichthyosis vulgaris phenotype, antisense profilaggrin RNA has more broad-reaching effects on in vitro differentiation of rat epidermal keratinocytes.

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Year:  1993        PMID: 7688400     DOI: 10.1111/1523-1747.ep12363609

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN: 0022-202X            Impact factor:   8.551


  5 in total

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Authors:  Xiaoyou Shi; Liping Wang; J David Clark; Wade S Kingery
Journal:  Regul Pept       Date:  2013-08-17

2.  Optimization of filaggrin expression and processing in cultured rat keratinocytes.

Authors:  Sudeshna M Chatterjea; Katheryn A Resing; William Old; Wilas Nirunsuksiri; Philip Fleckman
Journal:  J Dermatol Sci       Date:  2010-11-13       Impact factor: 4.563

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Authors:  Xiaoyou Shi; Liping Wang; Xiangqi Li; Peyman Sahbaie; Wade S Kingery; J David Clark
Journal:  Anesth Analg       Date:  2011-05-19       Impact factor: 5.108

4.  miR-203 regulates nociceptive sensitization after incision by controlling phospholipase A2 activating protein expression.

Authors:  Yuan Sun; Xiang-Qi Li; Peyman Sahbaie; Xiao-You Shi; Wen-Wu Li; De-Yong Liang; J David Clark
Journal:  Anesthesiology       Date:  2012-09       Impact factor: 7.892

5.  MUP-4 is a novel transmembrane protein with functions in epithelial cell adhesion in Caenorhabditis elegans.

Authors:  L Hong; T Elbl; J Ward; C Franzini-Armstrong; K K Rybicka; B K Gatewood; D L Baillie; E A Bucher
Journal:  J Cell Biol       Date:  2001-07-23       Impact factor: 10.539

  5 in total

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