-
Something wrong with this record ?
Microtubule nucleation in mouse bone marrow-derived mast cells is regulated by the concerted action of GIT1/βPIX proteins and calcium
V. Sulimenko, Z. Hájková, M. Černohorská, T. Sulimenko, V. Sládková, L. Dráberová, S. Vinopal, E. Dráberová, P. Dráber,
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
NT14467
MZ0
CEP Register
Digital library NLK
Full text - Article
Source
NLK
Free Medical Journals
from 1998 to 1 year ago
Freely Accessible Science Journals
from 1998-01-01 to 1 year ago
Open Access Digital Library
from 1998-01-01
- MeSH
- Bone Marrow Cells cytology MeSH
- Rho Guanine Nucleotide Exchange Factors metabolism MeSH
- Mast Cells cytology MeSH
- Microtubules metabolism MeSH
- Mice, Inbred BALB C MeSH
- Mice MeSH
- GTPase-Activating Proteins metabolism MeSH
- Cell Cycle Proteins metabolism MeSH
- Calcium metabolism MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Ag-mediated activation of mast cells initiates signaling events leading to Ca(2+) response, release of allergic mediators from cytoplasmic granules, and synthesis of cytokines and chemokines. Although microtubule rearrangement during activation has been described, the molecular mechanisms that control their remodeling are largely unknown. Microtubule nucleation is mediated by complexes that are formed by γ-tubulin and γ-tubulin complex proteins. In this study, we report that, in bone marrow-derived mast cells (BMMCs), γ-tubulin interacts with p21-activated kinase interacting exchange factor β (βPIX) and G protein-coupled receptor kinase-interacting protein (GIT)1. Microtubule regrowth experiments showed that the depletion of βPIX in BMMCs stimulated microtubule nucleation, whereas depletion of GIT1 led to the inhibition of nucleation compared with control cells. Phenotypic rescue experiments confirmed that βPIX and GIT1 represent negative and positive regulators of microtubule nucleation in BMMCs, respectively. Live-cell imaging disclosed that both proteins are associated with centrosomes. Immunoprecipitation and pull-down experiments revealed that an enhanced level of free cytosolic Ca(2+) affects γ-tubulin properties and stimulates the association of GIT1 and γ-tubulin complex proteins with γ-tubulin. Microtubule nucleation also was affected by Ca(2+) level. Moreover, in activated BMMCs, γ-tubulin formed complexes with tyrosine-phosphorylated GIT1. Further experiments showed that GIT1 and βPIX are involved in the regulation of such important physiological processes as Ag-induced chemotaxis and degranulation. Our study provides for the first time, to our knowledge, a possible mechanism for the concerted action of tyrosine kinases, GIT1/βPIX proteins, and Ca(2+) in the propagation of signals leading to the regulation of microtubule nucleation in activated mast cells.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc15031418
- 003
- CZ-PrNML
- 005
- 20191022094106.0
- 007
- ta
- 008
- 151005s2015 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.4049/jimmunol.1402459 $2 doi
- 035 __
- $a (PubMed)25821222
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Sulimenko, Vadym $u Department of Biology of Cytoskeleton, Institute of Molecular Genetics, Academy of Sciences of the Czech Republic, CZ-142 20 Prague 4, Czech Republic; $7 xx0117682
- 245 10
- $a Microtubule nucleation in mouse bone marrow-derived mast cells is regulated by the concerted action of GIT1/βPIX proteins and calcium / $c V. Sulimenko, Z. Hájková, M. Černohorská, T. Sulimenko, V. Sládková, L. Dráberová, S. Vinopal, E. Dráberová, P. Dráber,
- 520 9_
- $a Ag-mediated activation of mast cells initiates signaling events leading to Ca(2+) response, release of allergic mediators from cytoplasmic granules, and synthesis of cytokines and chemokines. Although microtubule rearrangement during activation has been described, the molecular mechanisms that control their remodeling are largely unknown. Microtubule nucleation is mediated by complexes that are formed by γ-tubulin and γ-tubulin complex proteins. In this study, we report that, in bone marrow-derived mast cells (BMMCs), γ-tubulin interacts with p21-activated kinase interacting exchange factor β (βPIX) and G protein-coupled receptor kinase-interacting protein (GIT)1. Microtubule regrowth experiments showed that the depletion of βPIX in BMMCs stimulated microtubule nucleation, whereas depletion of GIT1 led to the inhibition of nucleation compared with control cells. Phenotypic rescue experiments confirmed that βPIX and GIT1 represent negative and positive regulators of microtubule nucleation in BMMCs, respectively. Live-cell imaging disclosed that both proteins are associated with centrosomes. Immunoprecipitation and pull-down experiments revealed that an enhanced level of free cytosolic Ca(2+) affects γ-tubulin properties and stimulates the association of GIT1 and γ-tubulin complex proteins with γ-tubulin. Microtubule nucleation also was affected by Ca(2+) level. Moreover, in activated BMMCs, γ-tubulin formed complexes with tyrosine-phosphorylated GIT1. Further experiments showed that GIT1 and βPIX are involved in the regulation of such important physiological processes as Ag-induced chemotaxis and degranulation. Our study provides for the first time, to our knowledge, a possible mechanism for the concerted action of tyrosine kinases, GIT1/βPIX proteins, and Ca(2+) in the propagation of signals leading to the regulation of microtubule nucleation in activated mast cells.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a buňky kostní dřeně $x cytologie $7 D001854
- 650 _2
- $a vápník $x metabolismus $7 D002118
- 650 _2
- $a proteiny buněčného cyklu $x metabolismus $7 D018797
- 650 _2
- $a proteiny aktivující GTPasu $x metabolismus $7 D020690
- 650 _2
- $a mastocyty $x cytologie $7 D008407
- 650 _2
- $a myši $7 D051379
- 650 _2
- $a myši inbrední BALB C $7 D008807
- 650 _2
- $a mikrotubuly $x metabolismus $7 D008870
- 650 _2
- $a faktory zaměňující Rho guanin nukleotidy $x metabolismus $7 D064067
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Hájková, Zuzana $u Department of Biology of Cytoskeleton, Institute of Molecular Genetics, Academy of Sciences of the Czech Republic, CZ-142 20 Prague 4, Czech Republic; Department of Cell Biology, Faculty of Science, Charles University Prague, CZ-128 43 Prague 2, Czech Republic; and.
- 700 1_
- $a Černohorská, Markéta $u Department of Biology of Cytoskeleton, Institute of Molecular Genetics, Academy of Sciences of the Czech Republic, CZ-142 20 Prague 4, Czech Republic; Department of Cell Biology, Faculty of Science, Charles University Prague, CZ-128 43 Prague 2, Czech Republic; and.
- 700 1_
- $a Sulimenko, Tetyana $u Department of Biology of Cytoskeleton, Institute of Molecular Genetics, Academy of Sciences of the Czech Republic, CZ-142 20 Prague 4, Czech Republic; $7 xx0117681
- 700 1_
- $a Sládková, Vladimíra $u Department of Biology of Cytoskeleton, Institute of Molecular Genetics, Academy of Sciences of the Czech Republic, CZ-142 20 Prague 4, Czech Republic;
- 700 1_
- $a Dráberová, Lubica $u Department of Signal Transduction, Institute of Molecular Genetics, Academy of Sciences of the Czech Republic, CZ-142 20 Prague 4, Czech Republic. $7 xx0065233
- 700 1_
- $a Vinopal, Stanislav $u Department of Biology of Cytoskeleton, Institute of Molecular Genetics, Academy of Sciences of the Czech Republic, CZ-142 20 Prague 4, Czech Republic;
- 700 1_
- $a Dráberová, Eduarda $u Department of Biology of Cytoskeleton, Institute of Molecular Genetics, Academy of Sciences of the Czech Republic, CZ-142 20 Prague 4, Czech Republic; $7 xx0065234
- 700 1_
- $a Dráber, Pavel $u Department of Biology of Cytoskeleton, Institute of Molecular Genetics, Academy of Sciences of the Czech Republic, CZ-142 20 Prague 4, Czech Republic; paveldra@img.cas.cz. $7 xx0065228
- 773 0_
- $w MED00002741 $t Journal of immunology (Baltimore, Md. 1950) $x 1550-6606 $g Roč. 194, č. 9 (2015), s. 4099-4111
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/25821222 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20151005 $b ABA008
- 991 __
- $a 20191022094539 $b ABA008
- 999 __
- $a ok $b bmc $g 1092294 $s 914544
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2015 $b 194 $c 9 $d 4099-4111 $e 20150327 $i 1550-6606 $m The Journal of immunology $n J Immunol $x MED00002741
- GRA __
- $a NT14467 $p MZ0
- LZP __
- $a Pubmed-20151005