Original Article
Subject Category: Keratinocytes/Epidermis
Journal of Investigative Dermatology (2003) 121, 110–119; doi:10.1046/j.1523-1747.2003.12304.x
Constitutive Overexpression of Human Telomerase Reverse Transcriptase but Not c-myc Blocks Terminal Differentiation In Human HaCaT Skin Keratinocytes
Ana Cerezo1, Hans-Jürgen Stark*,1, Sharareh Moshir and Petra Boukamp
- German Cancer Research Center (DKFZ), Division of Differentiation and Carcinogenesis, Heidelberg, Germany
- *DKFZ, Division of Differentiation and Carcinogenesis Heidelberg, Germany
Correspondence: Dr Petra Boukamp., German Cancer Research Center (DKFZ), Division Genetics of Skin Carcinogenesis, Im Neuenheimer Feld 280, 69120 Heidelberg, Germany. Email: P.Boukamp@DKFZ-Heidelberg.de
1Both authors contributed equally to the work.
Received 10 October 2002; Revised 24 January 2003; Accepted 15 February 2003; Published online 30 June 2003.
Abstract
Formation of a well structured epidermis strictly depends on a tight balance between proliferation and differentiation. Accordingly, telomerase, which is restricted to proliferating cells, is downregulated with differentiation. It is unclear, however, whether this inhibition is essential to or only a consequence of the differentiation process. By studying different variants of the HaCaT skin keratinocytes we now show that constitutive overexpression of human telomerase reverse transcriptase (hTERT) in HaCaT-TERT cells (lacking its own differentiation-sensitive promoter) and constitutive expression of the c-myc gene in HaCaT-myc cells caused increased proliferation in conventional cultures; however, this proliferative advantage was not maintained in tissue-like organotypic cocultures. Despite reduced stratification, HaCaT-myc cells were still able to develop a fully differentiated epithelium. HaCaT-TERT cultures, on the other hand, expressed all markers of early but not of terminal differentiation. The failure to differentiate terminally was observed in hTERT mass cultures and individual clones and correlated with an intense nuclear hTERT staining of the uppermost cells of the HaCaT-TERT epithelia. Thus, our data suggest that constitutive overexpression of hTERT does not interfere with epidermal differentiation per se but blocks the terminal stage of differentiation and therefore indicates that hTERT/telomerase plays an active part in the regulatory pathway of epidermal differentiation.
Keywords:
apoptosis, differentiation markers, organotypic cocultures, proliferation, telomerase
Abbreviations:
BrdU, bromodeoxyuridine; hTERT, human telomerase reverse transcriptase; OTC, organotypic coculture; TUNEL, terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate nick end-labelling



