Kolloquiumsvortrag (MAWI), Jan Lammerding, Meinig School of Biomedical Engineering & Weill Institute for Cell and Molecular Biology Cornell University/ am 11.06.2018
11.06.2018 von 17:15 bis 18:00
Institute Ostufer, Geb. D, "Aquarium", Kaiserstr. 2, 24143 Kiel
Titel: Squish and squeeze – Nuclear mechanics and mechanotransduction in physiology and disease
Abstract: The nucleus is the characteristic feature of eukaryotic cells and houses the genomic information of the cell. The Lammerding laboratory is combining cell and molecular biology approaches with microfabricated devices that mimic physiological environments, live-cell microscopy, and in vivo models to investigate how physical forces acting on the nucleus, for example, in contracting muscle cells or during migration of cells through tight interstitial spaces, can challenge the integrity of the nucleus, alter its structure, and cause genomic and transcriptional changes. These processes play important roles in cellular mechanotransduction, i.e., the ability of cells to convert mechanical stimuli into biochemical signals, but can also contribute to various diseases when the nuclear structure is perturbed by mutations or altered protein expression. In particular, mutations in the nuclear envelope proteins lamin A/C are responsible for a broad spectrum of diseases (laminopathies), including Emery-Dreifuss muscular dystrophy (EDMD) and dilated cardiomyopathy. The fact that most mutations result in highly tissue-specific disease phenotypes primarily affecting skeletal and cardiac muscles, in spite of the near ubiquitous expression of lamins A/C, suggest that lamin mutations may render cells more sensitive to mechanical stress, which then causes progressive cell failure in mechanically stressed tissues. I will discuss our recent findings that highlight the importance of lamins A/C in mediating nuclear stability and mechanotransduction in mechanically stressed cells and tissues. At the same time, increased nuclear deformability, caused for example by reduced levels of lamins A/C, can promote cell migration through tight spaces with cross-sections smaller than the nuclear diameter, where the large size and rigidity of the nucleus can constitute a rate-limiting factor. I will present recent findings that demonstrate the importance of nuclear mechanics during cell migration in confined environments in vitro and in vivo, as well as the functional consequences of cells having to squeeze their large nuclei through tight interstitial spaces and small pores in the extracellular matrix network, with a particular focus on breast cancer.