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Continuous, label-free, 96-well-based determination of cell migration using confluence measurement.
Mayr, Christian; Beyreis, Marlena; Dobias, Heidemarie; Gaisberger, Martin; Fuchs, Julia; Pichler, Martin; Ritter, Markus; Jakab, Martin; Helm, Katharina; Neureiter, Daniel; Kiesslich, Tobias.
Afiliação
  • Mayr C; a Institute of Physiology and Pathophysiology, Laboratory for Tumour Biology and Experimental Therapies (TREAT) , Paracelsus Medical University Salzburg , Salzburg , Austria.
  • Beyreis M; b Department of Internal Medicine I , Paracelsus Medical University/Salzburger Landeskliniken (SALK) , Salzburg , Austria.
  • Dobias H; a Institute of Physiology and Pathophysiology, Laboratory for Tumour Biology and Experimental Therapies (TREAT) , Paracelsus Medical University Salzburg , Salzburg , Austria.
  • Gaisberger M; c Institute of Physiology and Pathophysiology, Laboratory of Functional and Molecular Membrane Physiology (FMMP) , Paracelsus Medical University Salzburg , Salzburg , Austria.
  • Fuchs J; d Gastein Research Institute, Institute of Physiology and Pathophysiology , Paracelsus Medical University Salzburg , Salzburg , Austria.
  • Pichler M; d Gastein Research Institute, Institute of Physiology and Pathophysiology , Paracelsus Medical University Salzburg , Salzburg , Austria.
  • Ritter M; e Ludwig Boltzmann Institute for Arthritis and Rehabilitation, Institute of Physiology and Pathophysiology , Paracelsus Medical University Salzburg , Salzburg , Austria.
  • Jakab M; d Gastein Research Institute, Institute of Physiology and Pathophysiology , Paracelsus Medical University Salzburg , Salzburg , Austria.
  • Helm K; f Division of Oncology, Department of Internal Medicine , Medical University Graz , Graz , Austria.
  • Neureiter D; g Department of Experimental Therapeutics , The UT MD Anderson Cancer Center , Houston / TX , USA.
  • Kiesslich T; a Institute of Physiology and Pathophysiology, Laboratory for Tumour Biology and Experimental Therapies (TREAT) , Paracelsus Medical University Salzburg , Salzburg , Austria.
Cell Adh Migr ; 13(1): 76-82, 2019 12.
Article em En | MEDLINE | ID: mdl-30295122
Cellular migration is essential in diverse physiological and pathophysiological processes. Here, we present a protocol for quantitative analysis of migration using confluence detection allowing continuous, non-endpoint measurement with minimal hands-on time under cell incubator conditions. Applicability was tested using substances which enhance (EGF) or inhibit (cytochalasin D, ouabain) migration. Using a gap-closure assay we demonstrate that automated confluence detection monitors cellular migration in the 96-well microplate format. Quantification by % confluence, % cell free-area or % confluence in cell-free area against time, allows detailed analysis of cellular migration. The study describes a practicable approach for continuous, non-endpoint measurement of migration in 96-well microplates and for detailed data analysis, which allows for medium/high-throughput analysis of cellular migration in vitro.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Bioensaio / Movimento Celular / Proliferação de Células / Adenocarcinoma de Pulmão Tipo de estudo: Guideline Limite: Humans Idioma: En Revista: Cell Adh Migr Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Bioensaio / Movimento Celular / Proliferação de Células / Adenocarcinoma de Pulmão Tipo de estudo: Guideline Limite: Humans Idioma: En Revista: Cell Adh Migr Ano de publicação: 2019 Tipo de documento: Article