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Pellikka, M.

Publications and source records attributed to Pellikka, M..

3 recordsLinked to original sources

Mitotic polarity oscillation promotes epithelial tumor progression

Mitosis of epithelial cells requires a transient loss of epithelial polarity [1-5]. However, the nature of this mitotic polarity oscillation and its functional consequences for epithelial development are not fully understood. Here we show that the Crumbs (Crb) complex, a key regulator of epithelial polarity, is lost from the membrane during mitosis, and the Crb mutant phenotype is ameliorated when cell division is inhibited. Remarkably, an essential requirement of Crb for epithelial polarity is fully suspended when cell division is blocked in conjunction with inhibition of either cell ingression or cell intercalation. We conclude that the amount of morphogenetic stress induced by mitosis, ingression, and intercalation determines the requirement for Crb. Increased cell division and loss of cell polarity are two main drivers of epithelial cancer [6-8]. Maintaining epithelial polarity is important for limiting proliferation. Whether the loss of polarity during mitosis impacts tissue growth is less clear. We show that increasing cell division in a morphogenetically quiet epithelium not only increases tissue size but also causes hyperplastic to neoplastic transition. Conversely, reducing cell division restores epithelial polarity in neoplastic tissue of tumor mutants. Taken together, our study revealed that a major function of polarity factors in epithelial maintenance is to counteract morphogenetic stress. Moreover, we propose a feedforward mechanism that links cell division and the loss of polarity as a key driver of epithelial cancer.

cell biology↗

Crumbs complex-directed apical membrane dynamics in epithelial cell ingression

Epithelial cells often leave their tissue context and ingress to form new cell types or acquire migratory ability to move to distant sites during development and tumor progression. Cell lose their apical membrane and epithelial adherens junctions during ingression. However, how factors that organize apical-basal polarity contribute to ingression is unknown. Here, we show that the dynamic regulation of the apical Crumbs polarity complex is crucial for normal neural stem cell ingression. Crumbs endocytosis and recycling allow ingression to occur in a normal timeframe. During early ingression, Crumbs and its complex partner the RhoGEF Cysts support myosin and apical constriction to ensure robust ingression dynamics. During late ingression, the E3-ubiquitin ligase Neuralized facilitates the disassembly of the Crumbs complex and the rapid endocytic removal of the apical cell domain. Our findings reveal a mechanism integrating cell fate, apical polarity, endocytosis, vesicle trafficking, and actomyosin contractility to promote cell ingression, a fundamental morphogenetic process observed in animal development and cancer.

developmental biology↗

The RhoGEF Cysts couples apical polarity proteins to Rho and myosin activity at adherens junctions

The spatio-temporal regulation of small Rho GTPases is crucial for the dynamic stability of epithelial tissues. However, how RhoGTPase activity is controlled during development remains largely unknown. To explore the regulation of Rho GTPases in vivo we analyzed the Rho GTPase guanine nucleotide exchange factor (RhoGEF) Cysts, the Drosophila orthologue of mammalian p114RhoGEF, GEF-H1, p190RhoGEF, and AKAP-13. Loss of Cysts causes a phenotype that closely resemble the mutant phenotype of the apical polarity regulator Crumbs. This phenotype can be suppressed by the loss of basolateral polarity proteins suggesting that Cysts in an integral component of the apical polarity protein network. Cysts activates Rho at adherens junctions to promote junctional enrichment of myosin II, which requires the RhoGEF domain and the coiled-coil domain containing C-terminal region of Cysts. Cysts recruitment to the apico-lateral cortex depends on Crumbs and Bazooka/Par3 and requires multiple domains within Cysts including the C-terminal region. Together, our findings indicate that Cysts links apical polarity proteins to Rho1 and myosin activation at adherens junctions to support junctional and epithelial integrity in the Drosophila ectoderm.

cell biology↗