TY - JOUR
T1 - Distinct localizations and roles of non-muscle myosin II during proplatelet formation and platelet release
AU - Badirou, I.
AU - Pan, J.
AU - Souquere, S.
AU - Legrand, C.
AU - Pierron, G.
AU - Wang, A.
AU - Eckly, A.
AU - Roy, A.
AU - Gachet, C.
AU - Vainchenker, W.
AU - Chang, Y.
AU - Léon, C.
N1 - Publisher Copyright:
© 2015 International Society on Thrombosis and Haemostasis.
PY - 2015/5/1
Y1 - 2015/5/1
N2 - Background: At the end of maturation, megakaryocytes (MKs) form long cytoplasmic extensions called proplatelets (PPT). Enormous changes in cytoskeletal structures cause PPT to extend further, to re-localize organelles such as mitochondria and to fragment, leading to platelet release. Two non-muscle myosin IIs (NMIIs) are expressed in MKs; however, only NMII-A (MYH9), but not NMII-B (MYH10), is expressed in mature MKs and is implicated in PPT formation. Objectives: To provide in vivo evidence on the specific role of NMII-A and IIB in MK PPT formation. Methods: We studied two transgenic mouse models in which non-muscle myosin heavy chain (NMHC) II-A was genetically replaced either by II-B or by a chimeric NMHCII that combined the head domain of II-A with the rod and tail domains of II-B. Results and Conclusions: This work demonstrates that the kinetic properties of NM-IIA, depending on the N-terminal domain, render NMII-A the better NMII candidate to control PPT formation. Furthermore, the carboxyl-terminal domain determines myosin II localization in the constriction region of PPT and is responsible for the specific role of NMII in platelet release.
AB - Background: At the end of maturation, megakaryocytes (MKs) form long cytoplasmic extensions called proplatelets (PPT). Enormous changes in cytoskeletal structures cause PPT to extend further, to re-localize organelles such as mitochondria and to fragment, leading to platelet release. Two non-muscle myosin IIs (NMIIs) are expressed in MKs; however, only NMII-A (MYH9), but not NMII-B (MYH10), is expressed in mature MKs and is implicated in PPT formation. Objectives: To provide in vivo evidence on the specific role of NMII-A and IIB in MK PPT formation. Methods: We studied two transgenic mouse models in which non-muscle myosin heavy chain (NMHC) II-A was genetically replaced either by II-B or by a chimeric NMHCII that combined the head domain of II-A with the rod and tail domains of II-B. Results and Conclusions: This work demonstrates that the kinetic properties of NM-IIA, depending on the N-terminal domain, render NMII-A the better NMII candidate to control PPT formation. Furthermore, the carboxyl-terminal domain determines myosin II localization in the constriction region of PPT and is responsible for the specific role of NMII in platelet release.
KW - Megakaryocyte
KW - Non-muscle myosin type IIA
KW - Non-muscle myosin type IIB
KW - Platelet
KW - Stem cell
UR - http://www.scopus.com/inward/record.url?scp=84928768726&partnerID=8YFLogxK
U2 - 10.1111/jth.12887
DO - 10.1111/jth.12887
M3 - Article
C2 - 25736522
AN - SCOPUS:84928768726
SN - 1538-7933
VL - 13
SP - 851
EP - 859
JO - Journal of Thrombosis and Haemostasis
JF - Journal of Thrombosis and Haemostasis
IS - 5
ER -