TY - JOUR
T1 - Myosin IIB assembly state determines its mechanosensitive dynamics
AU - Schiffhauer, Eric S.
AU - Ren, Yixin
AU - Iglesias, Vicente A.
AU - Kothari, Priyanka
AU - Iglesias, Pablo A.
AU - Robinson, Douglas N.
N1 - Funding Information:
This work was supported by grants from National Institutes of Health (GM66817 and GM109863) and Defense Advanced Research Projects Agency (HR0011-16-C-0139). National Institutes of Health grant S10 OD016374 supported the purchase of the FCS instrument. The authors declare no competing financial interests.
Publisher Copyright:
© 2019 Schiffhauer et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license
PY - 2019/3/1
Y1 - 2019/3/1
N2 - Dynamical cell shape changes require a highly sensitive cellular system that can respond to chemical and mechanical inputs. Myosin IIs are key players in the cell’s ability to react to mechanical inputs, demonstrating an ability to accumulate in response to applied stress. Here, we show that inputs that influence the ability of myosin II to assemble into filaments impact the ability of myosin to respond to stress in a predictable manner. Using mathematical modeling for Dictyostelium myosin II, we predict that myosin II mechanoresponsiveness will be biphasic with an optimum established by the percentage of myosin II assembled into bipolar filaments. In HeLa and NIH 3T3 cells, heavy chain phosphorylation of NMIIB by PKCζ, as well as expression of NMIIA, can control the ability of NMIIB to mechanorespond by influencing its assembly state. These data demonstrate that multiple inputs to the myosin II assembly state integrate at the level of myosin II to govern the cellular response to mechanical inputs.
AB - Dynamical cell shape changes require a highly sensitive cellular system that can respond to chemical and mechanical inputs. Myosin IIs are key players in the cell’s ability to react to mechanical inputs, demonstrating an ability to accumulate in response to applied stress. Here, we show that inputs that influence the ability of myosin II to assemble into filaments impact the ability of myosin to respond to stress in a predictable manner. Using mathematical modeling for Dictyostelium myosin II, we predict that myosin II mechanoresponsiveness will be biphasic with an optimum established by the percentage of myosin II assembled into bipolar filaments. In HeLa and NIH 3T3 cells, heavy chain phosphorylation of NMIIB by PKCζ, as well as expression of NMIIA, can control the ability of NMIIB to mechanorespond by influencing its assembly state. These data demonstrate that multiple inputs to the myosin II assembly state integrate at the level of myosin II to govern the cellular response to mechanical inputs.
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U2 - 10.1083/jcb.201806058
DO - 10.1083/jcb.201806058
M3 - Article
C2 - 30655296
AN - SCOPUS:85062408838
SN - 0021-9525
VL - 218
SP - 895
EP - 908
JO - Journal of Cell Biology
JF - Journal of Cell Biology
IS - 3
ER -