2024
Linking planar polarity signalling to actomyosin contractility during vertebrate neurulation
NOVOTNÁ, Šárka; Lorena AGOSTINI MAIA; Katarzyna Anna RADASZKIEWICZ; Pavel ROUDNICKÝ; Jakub HARNOŠ et. al.Základní údaje
Originální název
Linking planar polarity signalling to actomyosin contractility during vertebrate neurulation
Autoři
NOVOTNÁ, Šárka ORCID (203 Česká republika, domácí); Lorena AGOSTINI MAIA (76 Brazílie, domácí); Katarzyna Anna RADASZKIEWICZ (616 Polsko, domácí); Pavel ROUDNICKÝ (203 Česká republika, domácí) a Jakub HARNOŠ (203 Česká republika, domácí)
Vydání
Open Biology, Royal Society, 2024, 2046-2441
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10605 Developmental biology
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 4.500 v roce 2023
Kód RIV
RIV/00216224:14310/24:00137747
Organizační jednotka
Přírodovědecká fakulta
UT WoS
001357928300002
EID Scopus
2-s2.0-85209909295
Klíčová slova anglicky
actomyosin contractility; planar cell polarity; vertebrates; neurulation; Xenopus embryos; MDCK cells
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 24. 3. 2025 00:23, Mgr. Eva Dubská
Anotace
V originále
Actomyosin contractility represents an ancient feature of eukaryotic cells participating in many developmental and homeostasis events, including tissue morphogenesis, muscle contraction and cell migration, with dysregulation implicated in various pathological conditions, such as cancer. At the molecular level, actomyosin comprises actin bundles and myosin motor proteins that are sensitive to posttranslational modifications like phosphorylation. While the molecular components of actomyosin are well understood, the coordination of contractility by extracellular and intracellular signals, particularly from cellular signalling pathways, remains incompletely elucidated. This study focuses on WNT/planar cell polarity (PCP) signalling, previously associated with actomyosin contractility during vertebrate neurulation. Our investigation reveals that the main cytoplasmic PCP proteins, Prickle and Dishevelled, interact with key actomyosin components such as myosin light chain 9 (MLC9), leading to its phosphorylation and localized activation. Using proteomics and microscopy approaches, we demonstrate that both PCP proteins actively control actomyosin contractility through Rap1 small GTPases in relevant in vitro and in vivo models. These findings unveil a novel mechanism of how PCP signalling regulates actomyosin contractility through MLC9 and Rap1 that is relevant to vertebrate neurulation.
Návaznosti
EF18_046/0015974, projekt VaV |
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GA22-06405S, projekt VaV |
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MUNI/J/0004/2021, interní kód MU |
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90242, velká výzkumná infrastruktura |
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90250, velká výzkumná infrastruktura |
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