-
Something wrong with this record ?
Vesicles modulate an actin network for asymmetric spindle positioning
Z Holubcova, G Howard, M Schuh
Language English Country Great Britain
Document type Research Support, Non-U.S. Gov't
NLK
ProQuest Central
from 2000-01-01 to 1 year ago
Medline Complete (EBSCOhost)
from 1999-05-01 to 2015-11-30
Health & Medicine (ProQuest)
from 2000-01-01 to 1 year ago
- MeSH
- Actins * metabolism MeSH
- Spindle Apparatus * metabolism MeSH
- Models, Biological MeSH
- Cytoplasmic Vesicles * metabolism MeSH
- Fluorescent Antibody Technique MeSH
- Microscopy, Confocal MeSH
- Cells, Cultured MeSH
- Myosin Type V metabolism MeSH
- Mice MeSH
- Oocytes cytology metabolism MeSH
- rab GTP-Binding Proteins * metabolism MeSH
- Myosin Heavy Chains metabolism MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Research Support, Non-U.S. Gov't MeSH
Actin networks drive many essential cellular processes, including cell migration, cytokinesis and tissue morphogenesis. However, how cells organize and regulate dynamic actin networks that consist of long, unbranched actin filaments is only poorly understood. This study in mouse oocytes reveals that cells can use vesicles as adaptable, motorized network nodes to regulate the dynamics and density of intracellular actin networks. In particular, Rab11a-positive vesicles drive the network dynamics in a myosin-Vb-dependent manner, and modulate the network density by sequestering and clustering the network's actin nucleators. We also report a simple way by which networks of different densities can be generated, namely by adjusting the number and volume of vesicles in the cell. This vesicle-based mechanism of actin network modulation is essential for asymmetric positioning of the meiotic spindle in mouse oocytes, a vital step in the development of a fertilizable egg in mammals.
References provided by Crossref.org
Komentář v: Cytoskeleton: Building actin networks on vesicles. [Nat Rev Mol Cell Biol. 2013]
- 000
- 00000naa a2200000 a 4500
- 001
- bmc17012730
- 003
- CZ-PrNML
- 005
- 20170412110626.0
- 007
- ta
- 008
- 170412s2013 xxk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1038/ncb2802 $2 doi
- 035 __
- $a (PubMed)23873150
- 040 __
- $a ABA008 $d ABA008 $e AACR2 $b cze
- 041 0_
- $a eng
- 044 __
- $a xxk
- 100 1_
- $a Holubcová, Zuzana $7 xx0122016 $u Medical Research Council, Laboratory of Molecular Biology, Cambridge CB2 0QH, UK
- 245 10
- $a Vesicles modulate an actin network for asymmetric spindle positioning / $c Z Holubcova, G Howard, M Schuh
- 500 __
- $a Komentář v: Cytoskeleton: Building actin networks on vesicles. [Nat Rev Mol Cell Biol. 2013]
- 520 9_
- $a Actin networks drive many essential cellular processes, including cell migration, cytokinesis and tissue morphogenesis. However, how cells organize and regulate dynamic actin networks that consist of long, unbranched actin filaments is only poorly understood. This study in mouse oocytes reveals that cells can use vesicles as adaptable, motorized network nodes to regulate the dynamics and density of intracellular actin networks. In particular, Rab11a-positive vesicles drive the network dynamics in a myosin-Vb-dependent manner, and modulate the network density by sequestering and clustering the network's actin nucleators. We also report a simple way by which networks of different densities can be generated, namely by adjusting the number and volume of vesicles in the cell. This vesicle-based mechanism of actin network modulation is essential for asymmetric positioning of the meiotic spindle in mouse oocytes, a vital step in the development of a fertilizable egg in mammals.
- 590 __
- $a bohemika - dle Pubmed
- 650 12
- $a aktiny $x metabolismus $7 D000199
- 650 02
- $a zvířata $7 D000818
- 650 02
- $a kultivované buňky $7 D002478
- 650 12
- $a cytoplazmatické vezikuly $x metabolismus $7 D022162
- 650 02
- $a ženské pohlaví $7 D005260
- 650 02
- $a fluorescenční protilátková technika $7 D005455
- 650 02
- $a myši $7 D051379
- 650 02
- $a konfokální mikroskopie $7 D018613
- 650 02
- $a biologické modely $7 D008954
- 650 02
- $a těžké řetězce myosinu $x metabolismus $7 D018995
- 650 02
- $a myosin typu V $x metabolismus $7 D024701
- 650 02
- $a oocyty $x cytologie $x metabolismus $7 D009865
- 650 12
- $a aparát dělícího vřeténka $x metabolismus $7 D008941
- 650 12
- $a rab proteiny vázající GTP $x metabolismus $7 D020691
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Howard, G.
- 700 1_
- $a Schuh, M.
- 773 0_
- $t Nature Cell Biology $g Roč. 15, č. 8 (2013), s. 937-947 $p Nat Cell Biol $x 1465-7392 $w MED00005249
- 856 40
- $u https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3797517/ $y plný text volně přístupný
- 910 __
- $a ABA008 $y 4 $z 0
- 990 __
- $a 20170412110510 $b ABA008
- 991 __
- $a 20170412110926 $b ABA008
- 999 __
- $a ok $b bmc $g 1198946 $s 973503
- BAS __
- $a 3
- BMC __
- $a 2013 $b 15 $c 8 $d 937-947 $i 1465-7392 $m Nature cell biology $x MED00005249
- LZP __
- $a 2017-B-LM