Self-improvement of keratinocyte differentiation defects during skin maturation in ABCA12-deficient harlequin ichthyosis model mice

Teruki Yanagi, Masashi Akiyama, Hiroshi Nishihara, Junko Ishikawa, Kaori Sakai, Yuki Miyamura, Ayano Naoe, Takashi Kitahara, Shinya Tanaka, Hiroshi Shimizu

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41 Citations (Scopus)


Harlequin ichthyosis (HI) is caused by loss-of-function mutations in the keratinocyte lipid transporter ABCA12. The patients often die in the first 1 or 2 weeks of life, although HI survivors' phenotypes improve within several weeks after birth. In order to clarify the mechanisms of phenotypic recovery, we studied grafted skin and keratinocytes from Abca12-disrupted (Abca12 -/-) mice showing abnormal lipid transport. Abca12-/- neonatal epidermis showed significantly reduced total ceramide amounts and aberrant ceramide composition. Immunofluorescence and immunoblotting of Abca12-/- neonatal epidermis revealed defective profilaggrin/ filaggrin conversion and reduced protein expression of the differentiation- specific molecules, loricrin, kallikrein 5, and transglutaminase 1, although their mRNA expression was up-regulated. In contrast, Abca12-/- skin grafts kept in a dry environment exhibited dramatic improvements in all these abnormalities. Increased transepidermal water loss, a parameter representing barrier defect, was remarkably decreased in grafted Abca12-/- skin. Ten-passage sub-cultured Abca12-/- keratinocytes showed restoration of intact ceramide distribution, differentiation-specific protein expression and profilaggrin/filaggrin conversion, which were defective in primary-cultures. Using cDNA microarray analysis, lipid transporters including four ATP-binding cassette transporters were up-regulated after sub-culture of Abca12 -/- keratinocytes compared with primary-culture. These results indicate that disrupted keratinocyte differentiation during the fetal development is involved in the pathomechanism of HI and, during maturation, Abca12-/- epidermal keratinocytes regain normal differentiation processes. This restoration may account for the skin phenotype improvement observed in HI survivors.

Original languageEnglish
Pages (from-to)106-118
Number of pages13
JournalAmerican Journal of Pathology
Issue number1
Publication statusPublished - 2010 Jul
Externally publishedYes

ASJC Scopus subject areas

  • Pathology and Forensic Medicine


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