Hauke, Lara

[["dc.bibliographiccitation.firstpage","263"],["dc.bibliographiccitation.lastpage","282"],["dc.bibliographiccitation.seriesnr","134"],["dc.contributor.author","Eltzner, Benjamin"],["dc.contributor.author","Hauke, Lara"],["dc.contributor.author","Huckemann, Stephan"],["dc.contributor.author","Rehfeldt, Florian"],["dc.contributor.author","Wollnik, Carina"],["dc.contributor.editor","Salditt, Tim"],["dc.contributor.editor","Egner, Alexander"],["dc.contributor.editor","Luke, D. Russell"],["dc.date.accessioned","2021-04-21T11:15:39Z"],["dc.date.available","2021-04-21T11:15:39Z"],["dc.date.issued","2020"],["dc.identifier.doi","10.1007/978-3-030-34413-9_10"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/84280"],["dc.relation","SFB 755: Nanoscale Photonic Imaging"],["dc.relation.crisseries","Topics in Applied Physics"],["dc.relation.doi","10.1007/978-3-030-34413-9"],["dc.relation.eisbn","978-3-030-34413-9"],["dc.relation.isbn","978-3-030-34412-2"],["dc.relation.ispartof","Nanoscale Photonic Imaging"],["dc.relation.ispartofseries","Topics in Applied Physics; 134"],["dc.relation.orgunit","Institut für Röntgenphysik"],["dc.subject.gro","SFB 755"],["dc.title","A Statistical and Biophysical Toolbox to Elucidate Structure and Formation of Stress Fibers"],["dc.type","book_chapter"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","1595"],["dc.bibliographiccitation.issue","7"],["dc.bibliographiccitation.journal","International Journal of Molecular Sciences"],["dc.bibliographiccitation.volume","20"],["dc.contributor.author","Huber, René"],["dc.contributor.author","Attili/Abedalkhader, Rozan"],["dc.contributor.author","Küper, Daniela"],["dc.contributor.author","Hauke, Lara"],["dc.contributor.author","Lüns, Bernadette"],["dc.contributor.author","Brand, Korbinian"],["dc.contributor.author","Weissenborn, Karin"],["dc.contributor.author","Lichtinghagen, Ralf"],["dc.date.accessioned","2022-06-08T07:57:35Z"],["dc.date.available","2022-06-08T07:57:35Z"],["dc.date.issued","2019"],["dc.description.abstract","Blood sampling with different anticoagulants alters matrix metalloproteinase (MMP-) 9 expression, thus influencing its concentration and diagnostic validity. Here, we aimed to evaluate the effects of different anticoagulants on MMP-9 regulation. MMP-9 expression was assessed in response to ethylenediaminetetraacetic acid, citrate, and high-/low-molecular-weight heparin (HMWH, LMWH) in co-culture experiments using THP-1, Jurkat, and HT cells (representing monocytes, T, and B cells). Triple and double cell line co-culture experiments revealed that HMWH treatment of THP-1 and Jurkat led to a significant MMP-9 induction, whereas other anticoagulants and cell type combinations had no effect. Supernatant of HMWH-treated Jurkat cells also induced MMP-9 in THP-1 suggesting monocytes as MMP-9 producers. HMWH-induced cytokine/chemokine secretion was assessed in co-culture supernatant, and the influence of cytokines/chemokines on MMP-9 production was analyzed. These experiments revealed that Jurkat-derived IL-16 and soluble intercellular adhesion molecule (sICAM-) 1 are able to induce MMP-9 and IL-8 production by THP-1. As a consequence, the increased MMP-9 expression found in HMWH blood samples may be influenced by HMWH-dependent secretion of IL-16 and sICAM-1 by T cells resulting in an increased production of MMP-9 and IL-8 by monocytes. IL-8, in turn, may support MMP-9 and its own expression in a positive autocrine feedback loop."],["dc.identifier.doi","10.3390/ijms20071595"],["dc.identifier.pii","ijms20071595"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/110141"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-575"],["dc.relation.eissn","1422-0067"],["dc.title","Cellular and Molecular Effects of High-Molecular-Weight Heparin on Matrix Metalloproteinase 9 Expression"],["dc.type","journal_article"],["dc.type.internalPublication","unknown"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","e0250749"],["dc.bibliographiccitation.issue","9"],["dc.bibliographiccitation.journal","PLOS ONE"],["dc.bibliographiccitation.volume","16"],["dc.contributor.author","Hauke, Lara"],["dc.contributor.author","Narasimhan, Shwetha"],["dc.contributor.author","Primeßnig, Andreas"],["dc.contributor.author","Kaverina, Irina"],["dc.contributor.author","Rehfeldt, Florian"],["dc.contributor.editor","Komarova, Yulia"],["dc.date.accessioned","2022-01-11T14:06:10Z"],["dc.date.available","2022-01-11T14:06:10Z"],["dc.date.issued","2021"],["dc.description.abstract","Focal adhesions (FAs) and associated actin stress fibers (SFs) form a complex mechanical system that mediates bidirectional interactions between cells and their environment. This linked network is essential for mechanosensing, force production and force transduction, thus directly governing cellular processes like polarization, migration and extracellular matrix remodeling. We introduce a tool for fast and robust coupled analysis of both FAs and SFs named the Focal Adhesion Filament Cross-correlation Kit (FAFCK). Our software can detect and record location, axes lengths, area, orientation, and aspect ratio of focal adhesion structures as well as the location, length, width and orientation of actin stress fibers. This enables users to automate analysis of the correlation of FAs and SFs and study the stress fiber system in a higher degree, pivotal to accurately evaluate transmission of mechanocellular forces between a cell and its surroundings. The FAFCK is particularly suited for unbiased and systematic quantitative analysis of FAs and SFs necessary for novel approaches of traction force microscopy that uses the additional data from the cellular side to calculate the stress distribution in the substrate. For validation and comparison with other tools, we provide datasets of cells of varying quality that are labelled by a human expert. Datasets and FAFCK are freely available as open source under the GNU General Public License."],["dc.description.abstract","Focal adhesions (FAs) and associated actin stress fibers (SFs) form a complex mechanical system that mediates bidirectional interactions between cells and their environment. This linked network is essential for mechanosensing, force production and force transduction, thus directly governing cellular processes like polarization, migration and extracellular matrix remodeling. We introduce a tool for fast and robust coupled analysis of both FAs and SFs named the Focal Adhesion Filament Cross-correlation Kit (FAFCK). Our software can detect and record location, axes lengths, area, orientation, and aspect ratio of focal adhesion structures as well as the location, length, width and orientation of actin stress fibers. This enables users to automate analysis of the correlation of FAs and SFs and study the stress fiber system in a higher degree, pivotal to accurately evaluate transmission of mechanocellular forces between a cell and its surroundings. The FAFCK is particularly suited for unbiased and systematic quantitative analysis of FAs and SFs necessary for novel approaches of traction force microscopy that uses the additional data from the cellular side to calculate the stress distribution in the substrate. For validation and comparison with other tools, we provide datasets of cells of varying quality that are labelled by a human expert. Datasets and FAFCK are freely available as open source under the GNU General Public License."],["dc.identifier.doi","10.1371/journal.pone.0250749"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/97843"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-507"],["dc.relation.eissn","1932-6203"],["dc.title","A Focal Adhesion Filament Cross-correlation Kit for fast, automated segmentation and correlation of focal adhesions and actin stress fibers in cells"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","846"],["dc.bibliographiccitation.issue","7"],["dc.bibliographiccitation.journal","Molecular Biology of the Cell"],["dc.bibliographiccitation.lastpage","851"],["dc.bibliographiccitation.volume","29"],["dc.contributor.author","Chizhik, Anna M."],["dc.contributor.author","Wollnik, Carina"],["dc.contributor.author","Ruhlandt, Daja"],["dc.contributor.author","Karedla, Narain"],["dc.contributor.author","Chizhik, Alexey I."],["dc.contributor.author","Hauke, Lara"],["dc.contributor.author","Hähnel, Dirk"],["dc.contributor.author","Gregor, Ingo"],["dc.contributor.author","Enderlein, Jörg"],["dc.contributor.author","Rehfeldt, Florian"],["dc.contributor.editor","Bassereau, Patricía"],["dc.date.accessioned","2020-12-10T18:16:05Z"],["dc.date.available","2020-12-10T18:16:05Z"],["dc.date.issued","2018"],["dc.description.abstract","We report a novel method, dual-color axial nanometric localization by metal--induced energy transfer, and combine it with Förster resonance energy transfer (FRET) for resolving structural details in cells on the molecular level. We demonstrate the capability of this method on cytoskeletal elements and adhesions in human mesenchymal stem cells. Our approach is based on fluorescence-lifetime-imaging microscopy and allows for precise determination of the three-dimensional architecture of stress fibers anchoring at focal adhesions, thus yielding crucial information to understand cell-matrix mechanics. In addition to resolving nanometric structural details along the z-axis, we use FRET to gain precise information on the distance between actin and vinculin at focal adhesions."],["dc.identifier.doi","10.1091/mbc.E17-05-0314"],["dc.identifier.eissn","1939-4586"],["dc.identifier.issn","1059-1524"],["dc.identifier.pmid","29444956"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/75048"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.relation.eissn","1939-4586"],["dc.relation.issn","1059-1524"],["dc.relation.issn","1939-4586"],["dc.title","Dual-color metal-induced and Förster resonance energy transfer for cell nanoscopy"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","1967"],["dc.bibliographiccitation.issue","4"],["dc.bibliographiccitation.journal","Biomedical Optics Express"],["dc.bibliographiccitation.volume","11"],["dc.contributor.author","Gortari, Antu Nehuen"],["dc.contributor.author","Bouchoule, Sophie"],["dc.contributor.author","Cambril, Edmond"],["dc.contributor.author","Cattoni, Andrea"],["dc.contributor.author","Hauke, Lara"],["dc.contributor.author","Enderlein, Jörg"],["dc.contributor.author","Rehfeldt, Florian"],["dc.contributor.author","Yacomotti, Alejandro"],["dc.date.accessioned","2020-12-10T18:42:00Z"],["dc.date.available","2020-12-10T18:42:00Z"],["dc.date.issued","2020"],["dc.identifier.doi","10.1364/BOE.385276"],["dc.identifier.eissn","2156-7085"],["dc.identifier.issn","2156-7085"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/77771"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.title","Metasurface-based total internal reflection microscopy"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]