Research output: Contribution to journal › Article › peer-review
Coordination of cytoskeletal dynamics and cell behaviour during Drosophila abdominal morphogenesis. / Pulido Companys, Pau; Norris, Anneliese; Bischoff, Marcus.
In: Journal of Cell Science, Vol. 133, No. 6, jcs235325, 30.03.2020.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Coordination of cytoskeletal dynamics and cell behaviour during Drosophila abdominal morphogenesis
AU - Pulido Companys, Pau
AU - Norris, Anneliese
AU - Bischoff, Marcus
N1 - This work was supported by the BBSRC (BB/M021084/1).
PY - 2020/3/30
Y1 - 2020/3/30
N2 - During morphogenesis, cells exhibit various behaviours, such as migration and constriction, which need to be coordinated. How this is achieved remains elusive. During morphogenesis of the Drosophila adult abdominal epidermis, larval epithelial cells (LECs) migrate directedly before constricting apically and undergoing apoptosis. Here, we study the mechanisms underlying the transition from migration to constriction. We show that LECs possess a pulsatile apical actomyosin network, and that a change in network polarity correlates with behavioural change. Exploring the properties of the contractile network, we find that cell contractility, as determined by myosin activity, has an impact on the behaviour of the network, as well as on cytoskeletal architecture and cell behaviour. Pulsed contractions occur only in cells with intermediate levels of contractility. Furthermore, increasing levels of the small Rho GTPase Rho1 disrupts pulsing, leading to cells that cycle between two states, characterised by a junctional cortical and an apicomedial actin network. Our results highlight that behavioural change relies on tightly controlled cellular contractility. Moreover, we show that constriction can occur without pulsing, raising questions why constricting cells pulse in some contexts but not in others.
AB - During morphogenesis, cells exhibit various behaviours, such as migration and constriction, which need to be coordinated. How this is achieved remains elusive. During morphogenesis of the Drosophila adult abdominal epidermis, larval epithelial cells (LECs) migrate directedly before constricting apically and undergoing apoptosis. Here, we study the mechanisms underlying the transition from migration to constriction. We show that LECs possess a pulsatile apical actomyosin network, and that a change in network polarity correlates with behavioural change. Exploring the properties of the contractile network, we find that cell contractility, as determined by myosin activity, has an impact on the behaviour of the network, as well as on cytoskeletal architecture and cell behaviour. Pulsed contractions occur only in cells with intermediate levels of contractility. Furthermore, increasing levels of the small Rho GTPase Rho1 disrupts pulsing, leading to cells that cycle between two states, characterised by a junctional cortical and an apicomedial actin network. Our results highlight that behavioural change relies on tightly controlled cellular contractility. Moreover, we show that constriction can occur without pulsing, raising questions why constricting cells pulse in some contexts but not in others.
KW - Cell migration
KW - Apical constriction
KW - Pulsed contractions
KW - Actomyosin contractility
KW - Drosophila
U2 - 10.1242/jcs.235325
DO - 10.1242/jcs.235325
M3 - Article
VL - 133
JO - Journal of Cell Science
JF - Journal of Cell Science
SN - 0021-9533
IS - 6
M1 - jcs235325
ER -
Research output: Contribution to journal › Article › peer-review
Research output: Chapter in Book/Report/Conference proceeding › Chapter
Research output: Contribution to journal › Article › peer-review
Research output: Contribution to journal › Article › peer-review
Research output: Contribution to journal › Article › peer-review
Research output: Contribution to journal › Article › peer-review
Research output: Contribution to journal › Article › peer-review
Research output: Contribution to journal › Article › peer-review
Research output: Contribution to journal › Article › peer-review
ID: 265898135