Dataset Information

Reduced PaxillinB localization to cell-substrate adhesions promotes cell migration in Dictyostelium.

ABSTRACT: Many cells adhere to extracellular matrix for efficient cell migration. This adhesion is mediated by focal adhesions, a protein complex linking the extracellular matrix to the intracellular cytoskeleton. Focal adhesions have been studied extensively in mesenchymal cells, but recent research in physiological contexts and amoeboid cells suggest focal adhesion regulation differs from the mesenchymal focal adhesion paradigm. We used Dictyostelium discoideum to uncover new mechanisms of focal adhesion regulation, as Dictyostelium are amoeboid cells that form focal adhesion-like structures for migration. We show that PaxillinB, the Dictyostelium homologue of Paxillin, localizes to dynamic focal adhesion-like structures during Dictyostelium migration. Unexpectedly, reduced PaxillinB recruitment to these structures increases Dictyostelium cell migration. Quantitative analysis of focal adhesion size and dynamics show that lack of PaxillinB recruitment to focal adhesions does not alter focal adhesion size, but rather increases focal adhesion turnover. These findings are in direct contrast to Paxillin function at focal adhesions during mesenchymal migration, challenging the established focal adhesion model.

SUBMITTER: Fierro Morales JC

PROVIDER: S-EPMC10983970 | biostudies-literature | 2024 Mar

REPOSITORIES: biostudies-literature

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Reduced cell-substrate adhesion formation promotes cell migration in <i>Dictyostelium</i>.

Fierro Morales Julio C JC Nguyen Thu T Nepal Sabin S Redfearn Chandler C Gale Bruce K BK Titus Margaret A MA Roh-Johnson Minna M

bioRxiv : the preprint server for biology 20250515

Many cells adhere to the extracellular matrix for efficient cell migration. This adhesion is mediated by focal adhesions, a protein complex linking the extracellular matrix to the intracellular cytoskeleton. Focal adhesions have been studied extensively in Metazoan mesenchymal cells, but recent research in physiological contexts and amoeboid cells suggest that focal adhesion regulation differs from the mesenchymal focal adhesion paradigm. While focal adhesion machinery predates the origin of Met ...[more]

PMID: 38562712

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Project description:BACKGROUND:Deregulated c-Abl activity has been intensively studied in a variety of solid tumors and leukemia. The class-I carcinogen Helicobacter pylori (Hp) activates the non-receptor tyrosine kinase c-Abl to phosphorylate the oncoprotein cytotoxin-associated gene A (CagA). The role of c-Abl in CagA-dependent pathways is well established; however, the knowledge of CagA-independent c-Abl processes is scarce. METHODS:c-Abl phosphorylation and localization were analyzed by immunostaining and immunofluorescence. Interaction partners were identified by tandem-affinity purification. Cell elongation and migration were analyzed in transwell-filter experiments. Apoptosis and cell survival were examined by FACS analyses and MTT assays. In mice experiments and human biopsies, the involvement of c-Abl in Hp pathogenesis was investigated. RESULTS:Here, we investigated the activity and subcellular localization of c-Abl in vitro and in vivo and unraveled the contribution of c-Abl in CagA-dependent and -independent pathways to gastric Hp pathogenesis. We report a novel mechanism and identified strong c-Abl threonine 735 phosphorylation (pAblT735) mediated by the type-IV secretion system (T4SS) effector D-glycero-β-D-manno-heptose-1,7-bisphosphate (βHBP) and protein kinase C (PKC) as a new c-Abl kinase. pAblT735 interacted with 14-3-3 proteins, which caused cytoplasmic retention of c-Abl, where it potentiated Hp-mediated cell elongation and migration. Further, the nuclear exclusion of pAblT735 attenuated caspase-8 and caspase-9-dependent apoptosis. Importantly, in human patients suffering from Hp-mediated gastritis c-Abl expression and pAblT735 phosphorylation were drastically enhanced as compared to type C gastritis patients or healthy individuals. Pharmacological inhibition using the selective c-Abl kinase inhibitor Gleevec confirmed that c-Abl plays an important role in Hp pathogenesis in a murine in vivo model. CONCLUSIONS:In this study, we identified a novel regulatory mechanism in Hp-infected gastric epithelial cells by which Hp determines the subcellular localization of activated c-Abl to control Hp-mediated EMT-like processes while decreasing cell death.

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Reduced PaxillinB localization to cell-substrate adhesions promotes cell migration in Dictyostelium.

Publications

Reduced cell-substrate adhesion formation promotes cell migration in <i>Dictyostelium</i>.

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Reduced PaxillinB localization to cell-substrate adhesions promotes cell migration in Dictyostelium.

Publications

Reduced cell-substrate adhesion formation promotes cell migration in &lt;i&gt;Dictyostelium&lt;/i&gt;.

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OmicsDI is part of the ELIXIR infrastructure

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Reduced cell-substrate adhesion formation promotes cell migration in <i>Dictyostelium</i>.