Isolation and Culture of Epidermolysis Bullosa Cells and Organotypic Skin Models.


Journal

Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969

Informations de publication

Date de publication:
2019
Historique:
entrez: 1 6 2019
pubmed: 31 5 2019
medline: 27 2 2020
Statut: ppublish

Résumé

Isolation and culture of keratinocytes from patients with different types of epidermolysis bullosa are sometimes challenging, because of the inherent adhesion defects of these cells. We routinely employ a well-established protocol for in vitro culture of these cells from small skin samples remaining after diagnostic procedures are performed. Keratinocytes and fibroblast can be used for downstream expression and functional studies or for construction of in vitro organotypic cocultures. These cells maintain main common characteristics of spreading, adhesion, migration, and survival, which depend on the underlying molecular defect.

Identifiants

pubmed: 31148087
doi: 10.1007/978-1-4939-9473-1_14
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

181-190

Références

Germain L, Rouabhia M, Guignard R, Carrier L, Bouvard V, Auger FA (1993) Improvement of human keratinocyte isolation and culture using thermolysin. Burns 19:99–104
doi: 10.1016/0305-4179(93)90028-7
Bruckner-Tuderman L, Has C (2014) Disorders of the cutaneous basement membrane zone--the paradigm of epidermolysis bullosa. Matrix Biol 33:29–34
doi: 10.1016/j.matbio.2013.07.007
Has C, He Y (2017) Focal adhesions in the skin: lessons learned from skin fragility disorders. Eur J Dermatol S1:8–11
Gagnoux-Palacios L, Vailly J, Durand-Clement M, Wagner E, Ortonne JP, Meneguzzi G (1996) Functional Re-expression of laminin-5 in laminin-gamma2-deficient human keratinocytes modifies cell morphology, motility, and adhesion. J Biol Chem 271:18437–18444
doi: 10.1074/jbc.271.31.18437
Herz C, Aumailley M, Schulte C, Schlötzer-Schrehardt U, Bruckner-Tuderman L, Has C (2006) Kindlin-1 is a phosphoprotein involved in regulation of polarity, proliferation, and motility of epidermal keratinocytes. J Biol Chem 281:36082–36090
doi: 10.1074/jbc.M606259200
Piccinni E, Di Zenzo G, Maurelli R, Dellambra E, Teson M, Has C, Zambruno G, Castiglia D (2013) Induction of senescence pathways in Kindler syndrome primary keratinocytes. Br J Dermatol 168:1019–1026
doi: 10.1111/bjd.12184
He Y, Maier K, Leppert J, Hausser I, Schwieger-Briel A, Weibel L, Theiler M, Kiritsi D, Busch H, Boerries M et al (2016) Monoallelic mutations in the translation initiation codon of KLHL24 cause skin fragility. Am J Hum Genet 99:1395–1404
doi: 10.1016/j.ajhg.2016.11.005
Maier K, He Y, Esser PR, Thriene K, Sarca D, Kohlhase J, Dengjel J, Martin L, Has C (2016) Single amino acid deletion in kindlin-1 results in partial protein degradation which can be rescued by chaperone treatment. J Invest Dermatol 136:920–929
doi: 10.1016/j.jid.2015.12.039
Stark H-J, Szabowski A, Fusenig NE, Maas-Szabowski N (2004) Organotypic cocultures as skin equivalents: a complex and sophisticated in vitro system. Biol Proced Online 6:55–60
doi: 10.1251/bpo72

Auteurs

Yinghong He (Y)

Department of Dermatology, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Cristina Has (C)

Department of Dermatology, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany. cristina.has@uniklinik-freiburg.de.

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