Cell cycle-dependent transitions in PCP protein mobility erase and restore planar cell polarity in mitosis

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AI-generated summary by claude@2026-07, 2026-07-16

This study shows that planar cell polarity proteins transition between mobile and stable states during the cell cycle, with increased mobility during mitosis and non-cell autonomous stabilization during cytokinesis to restore asymmetry.

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AI-generated deep summary by claude@2026-07, 2026-07-16 · read from full text

The study examined how planar cell polarity (PCP) proteins are transported and retained during mitosis, using live imaging and FRAP to track membrane-associated protein mobility as polarity asymmetry is temporarily lost and then restored. The authors found that PCP proteins become internalized into endocytic vesicles, and that membrane-associated PCP proteins show a marked increase in lateral mobility upon mitotic entry in a Plk1-dependent manner. Contrary to polarized vesicle delivery, asymmetry restoration in cytokinesis was not driven by targeted delivery; instead, proteins continued to diffuse laterally and were captured and stabilized via adhesive interactions with neighboring cells, with the authors proposing a transient diffusive state for robustness. This paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

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Abstract

ABSTRACT Central to our understanding of how cells establish polarity is deciphering how polarity proteins are transported to and retained at asymmetric positions. Here, in the context of planar cell polarity (PCP) remodeling in mitosis where asymmetry is transiently lost and restored, we show that PCP proteins transition between mobile and stable states in coordination with cell cycle progression. Live imaging and FRAP analyses reveal that, in addition to becoming internalized into endocytic vesicles, membrane-associated PCP proteins dramatically increase their lateral mobility upon mitotic entry in a Plk1-dependent manner. Unexpectedly, asymmetry is not restored in cytokinesis via polarized delivery of PCP-protein containing vesicles. Rather, PCP proteins continue to diffuse laterally during cytokinesis where they are captured and stabilized non-cell autonomously through adhesive interactions with neighbors. We propose that a transient, laterally diffusive state in mitosis allows for flexibility and robustness in planar polarity as dividing cells change shape and rearrange.
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ABSTRACT Central to our understanding of how cells establish polarity is deciphering how polarity proteins are transported to and retained at asymmetric positions. Here, in the context of planar cell polarity (PCP) remodeling in mitosis where asymmetry is transiently lost and restored, we show that PCP proteins transition between mobile and stable states in coordination with cell cycle progression. Live imaging and FRAP analyses reveal that, in addition to becoming internalized into endocytic vesicles, membrane-associated PCP proteins dramatically increase their lateral mobility upon mitotic entry in a Plk1-dependent manner. Unexpectedly, asymmetry is not restored in cytokinesis via polarized delivery of PCP-protein containing vesicles. Rather, PCP proteins continue to diffuse laterally during cytokinesis where they are captured and stabilized non-cell autonomously through adhesive interactions with neighbors. We propose that a transient, laterally diffusive state in mitosis allows for flexibility and robustness in planar polarity as dividing cells change shape and rearrange. Competing Interest Statement The authors have declared no competing interest. Footnotes Author list has been updated such they are now listed in the correct order.

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