4.4 Article

Keratinocyte-based cell assays: their potential pitfalls

Journal

ARCHIVES OF DERMATOLOGICAL RESEARCH
Volume 304, Issue 9, Pages 765-768

Publisher

SPRINGER
DOI: 10.1007/s00403-012-1285-6

Keywords

Keratinocyte; EBS; Assay; Proliferation; Migration; Metabolic activity

Categories

Funding

  1. Slovenian Research Agency [J3-2274-0381, J3-3617-0381]

Ask authors/readers for more resources

As an in vitro model system, patient-derived epidermolysis bullosa simplex keratinocytes have had an immense impact on what we know today about keratin filament function and their role in disease development. In the absence of gene therapy, screening compound libraries for new or better drugs is another approach to improve existing treatments for genodermatoses. However in this study, we report of the potential pitfalls when using this type of cell lines as a reporter system. When cell lines with different genetic backgrounds are being used in cell-based assays, the greatest obstacle is to determine the most appropriate culture conditions (i.e., the composition of medium, number of cells plated and number of days in culture). We demonstrate how culture conditions can greatly interfere with the cellular response in cell-based assays (cell proliferation, metabolic activity and migration), potentially also giving rise to misleading data.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

Article Biochemistry & Molecular Biology

Revertant mosaicism repairs skin lesions in a patient with keratitis-ichthyosis-deafness syndrome by second-site mutations in connexin 26

Sanna Gudmundsson, Maria Wilbe, Sara Ekvall, Adam Ameur, Nicola Cahill, Ludmil B. Alexandrov, Marie Virtanen, Maritta Hellstrom Pigg, Anders Vahlquist, Hans Torma, Marie-Louise Bondeson

HUMAN MOLECULAR GENETICS (2017)

Letter Dermatology

Identification of mutations in SDR9C7 in six families with autosomal recessive congenital ichthyosis

A. Hotz, C. Fagerberg, A. Vahlquist, A. Bygum, H. Torma, M-A Rauschendorf, H. Zhang, L. Heinz, E. Bourrat, I. Hausser, V. Vestergaard, A. Dragomir, A. D. Zimmer, J. Fischer

BRITISH JOURNAL OF DERMATOLOGY (2018)

Article Dermatology

Quantitative image analysis of protein expression and colocalisation in skin sections

Hanqian Zhang, Maja Ericsson, Marie Virtanen, Simone Westroem, Carolina Waehlby, Anders Vahlquist, Hans Torma

EXPERIMENTAL DERMATOLOGY (2018)

Article Dermatology

Moisturizing treatment of patients with atopic dermatitis and ichthyosis vulgaris improves dry skin, but has a modest effect on gene expression regardless of FLG genotype

T. Hoppe, M. C. G. Winge, M. Bradley, M. Nordenskjold, A. Vahlquist, H. Torma, B. Berne

JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY (2015)

Article Biochemistry & Molecular Biology

A CYP26B1 Polymorphism Enhances Retinoic Acid Catabolism and May Aggravate Atherosclerosis

Olesya Krivospitskaya, Ali Ateia Elmabsout, Eva Sundman, Leif A. Soderstrom, Olga Ovchinnikova, Andreas C. Gidlof, Nikolai Scherbak, Giuseppe Danilo Norata, Ann Samnegard, Hans Torma, Samy M. Abdel-Halim, Jan-Hakan Jansson, Per Eriksson, Allan Sirsjo, Peder S. Olofsson

MOLECULAR MEDICINE (2012)

Article Multidisciplinary Sciences

siRNA Silencing of Proteasome Maturation Protein (POMP) Activates the Unfolded Protein Response and Constitutes a Model for KLICK Genodermatosis

Johanna Dahlqvist, Hans Torma, Jitendra Badhai, Niklas Dahl

PLOS ONE (2012)

Article Multidisciplinary Sciences

Cloning and Functional Studies of a Splice Variant of CYP26B1 Expressed in Vascular Cells

Ali Ateia Elmabsout, Ashok Kumawat, Patricia Saenz-Mendez, Olesya Krivospitskaya, Helena Savenstrand, Peder S. Olofsson, Leif A. Eriksson, Ake Strid, Guro Valen, Hans Torma, Allan Sirsjo

PLOS ONE (2012)

Article Dermatology

Patients with congenital ichthyosis and TGM1 mutations overexpress other ARCI genes in the skin: Part of a barrier repair response?

Hanqian Zhang, Maja Ericsson, Simone Westrom, Anders Vahiquist, Marie Virtanen, Hans Torma

EXPERIMENTAL DERMATOLOGY (2019)

Editorial Material Cell & Tissue Engineering

Induced pluripotent stem cell (iPSC) line from an epidermolysis bullosa simplex patient heterozygous for keratin 5 E475G mutation and with the Dowling Meara phenotype

Nikola Kolundzic, Preeti Khurana, Carl Hobbs, Marija Rogar, Sandra Ropret, Hans Torma, Dusko Ilic, Mirjana Liovic

STEM CELL RESEARCH (2019)

Review Dermatology

Ichthyosis: A Road Model for Skin Research

Anders Vahlquist, Hans Torma

ACTA DERMATO-VENEREOLOGICA (2020)

Review Dermatology

Inherited Nonsyndromic Ichthyoses: An Update on Pathophysiology, Diagnosis and Treatment

Anders Vahlquist, Judith Fischer, Hans Torma

AMERICAN JOURNAL OF CLINICAL DERMATOLOGY (2018)

Article Dermatology

Keratin gene mutations influence the keratinocyte response to DNA damage and cytokine induced apoptosis

Tina Zupancic, Gregor Sersa, Hans Torma, Ellen Birgitte Lane, Harald Herrmann, Radovan Komel, Mirjana Liovic

ARCHIVES OF DERMATOLOGICAL RESEARCH (2017)

No Data Available