CRM1 and chromosomal passenger complex component survivin are essential to normal mitosis progress and to preserve keratinocytes from mitotic abnormalities

• Published in: International journal of cosmetic science 2016-10, Vol.38 (5), p.452-461
• Main Authors: Labarrade, F., Botto, J.-M., Domloge, N.
• Format: Article
• Language: English
• Subjects: Adult; Biopsy; cell culture; Cell division; Cells, Cultured; Chromosomes; epidermal renewal; Exportin 1 Protein; Female; Humans; Inhibitor of Apoptosis Proteins - genetics; Inhibitor of Apoptosis Proteins - physiology; Karyopherins - genetics; Karyopherins - physiology; Keratinocytes - cytology; Kinases; Mitosis - physiology; mitotic catastrophe; Receptors, Cytoplasmic and Nuclear - genetics; Receptors, Cytoplasmic and Nuclear - physiology; Skin; skin barrier; skin physiology/structure; Survivin
• ISSN: 0142-5463; 1468-2494
• DOI: 10.1111/ics.12311

Objective Human epidermis provides the body a barrier against environmental assaults. To assume this function, the epidermis needs the renewal of keratinocytes allowed by constant mitosis, which replace the exfoliating corneocytes. Keratinocyte stem cells (KSCs) located in the basal epidermis are mitotically active, self‐renewing and govern the epithelial stratification by producing renewed source of keratinocytes. Protein complex such as the chromosomal passenger complex (CPC) allows the correct development of this process. The CPC is composed of four members: INCENP, survivin, borealin and aurora kinase B, and the disruption of the CPC during cell division induces mitotic spindle defects and improper repartition of chromosomes. The aim of our study was to investigate the implication of CRM1 and survivin in the progress of mitosis in skin keratinocytes. Methods Cultured human keratinocytes and skin biopsies were used in this study. KSCs‐enriched population of keratinocytes was isolated from total keratinocytes by differential attachment to a type IV collagen matrix. Survivin and CRM1 expression levels were assessed by immunofluorescence and immunoblotting. Specific siRNAs for each CPC member and for CRM1 were used to determine the relationship between these proteins. Survivin‐specific siRNA was used to induce the apparition of mitotic abnormalities in cultured keratinocytes. Results We demonstrated the ability of our compound ‘IV08.009’ to modulate the expression level of survivin and CRM1 in keratinocytes and in skin biopsies. We observed that members of the CPC are interdependent: siRNA‐induced inhibition of one component caused a decrease in the expression of all other CPC members. Downregulation of survivin or CRM1 induced mitotic abnormalities in keratinocytes. However, decreased number of mitotic abnormalities was observed in keratinocytes after ‘IV08.009’ application. Conclusion Basal keratinocytes may divide frequently during skin lifespan, and signs of deterioration could appear such as loss of protein factors required for correct mitosis. Our findings suggest that mitotic abnormalities can be prevented by the modulation of CRM1 and survivin. We demonstrated the ability of compound ‘IV08.009’ to efficiently protect cultured keratinocytes from mitotic abnormalities. Résumé Objectif L’épiderme humain fournit à l'organisme une barrière contre les agressions de l'environnement. Pour assumer cette fonction, l’épiderme a besoin d'un renouvellement cons