<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>25</volume><submitter>Kubouchi K</submitter><funding>Ministry of Education, Culture, Sports, Science and Technology</funding><pubmed_abstract>The role of Protein Kinase N2 (PKN2, also known as PRK2/PKNγ) in cell aggregate/spheroid formation in suspension culture was investigated using immortalized fibroblasts established from &lt;i>PKN2&lt;/i> &lt;sup>flox/flox&lt;/sup> mouse embryos. &lt;i>PKN2&lt;/i> &lt;sup>flox/flox&lt;/sup> cells formed cell aggregates in flat bottom low attachment well plates, such as 2% agar and poly-2-hydroxyethymethacrylate coated plates, however, Cre;&lt;i>PKN2&lt;/i> &lt;sup>flox/flox&lt;/sup> cells in which PKN2 was depleted by the introduction of Cre-recombinase rarely formed aggregates. Time-lapse analysis revealed that the velocity of Cre;&lt;i>PKN2&lt;/i> &lt;sup>flox/flox&lt;/sup> cell motility was significantly lower than that of &lt;i>PKN2&lt;/i> &lt;sup>flox/flox&lt;/sup> in a low attachment flat-bottom plate, which likely resulted in a lower cell-cel</pubmed_abstract><journal>Biochemistry and biophysics reports</journal><pagination>100895</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7787963</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>PKN2 is involved in aggregation and spheroid formation of fibroblasts in suspension culture by regulating cell motility and &lt;i>N-cadherin&lt;/i> expression.</pubmed_title><pmcid>PMC7787963</pmcid><pubmed_authors>Mukai H</pubmed_authors><pubmed_authors>Kubouchi K</pubmed_authors></additional><is_claimable>false</is_claimable><name>PKN2 is involved in aggregation and spheroid formation of fibroblasts in suspension culture by regulating cell motility and &lt;i>N-cadherin&lt;/i> expression.</name><description>The role of Protein Kinase N2 (PKN2, also known as PRK2/PKNγ) in cell aggregate/spheroid formation in suspension culture was investigated using immortalized fibroblasts established from &lt;i>PKN2&lt;/i> &lt;sup>flox/flox&lt;/sup> mouse embryos. &lt;i>PKN2&lt;/i> &lt;sup>flox/flox&lt;/sup> cells formed cell aggregates in flat bottom low attachment well plates, such as 2% agar and poly-2-hydroxyethymethacrylate coated plates, however, Cre;&lt;i>PKN2&lt;/i> &lt;sup>flox/flox&lt;/sup> cells in which PKN2 was depleted by the introduction of Cre-recombinase rarely formed aggregates. Time-lapse analysis revealed that the velocity of Cre;&lt;i>PKN2&lt;/i> &lt;sup>flox/flox&lt;/sup> cell motility was significantly lower than that of &lt;i>PKN2&lt;/i> &lt;sup>flox/flox&lt;/sup> in a low attachment flat-bottom plate, which likely resulted in a lower cell-cel</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Mar</publication><modification>2025-06-01T00:57:27.37Z</modification><creation>2025-06-01T00:57:27.37Z</creation></dates><accession>S-EPMC7787963</accession><cross_references><pubmed>33437883</pubmed><doi>10.1016/j.bbrep.2020.100895</doi></cross_references></HashMap>