-
Something wrong with this record ?
Yeast glucan particles enable intracellular protein delivery in Drosophila without compromising the immune system
A. Bajgar, I. Saloň, G. Krejčová, T. DoleŽal, M. Jindra, F. Štěpánek,
Language English Country Great Britain
Document type Journal Article
Grant support
NV16-27522A
MZ0
CEP Register
PubMed
31565713
DOI
10.1039/c9bm00539k
Knihovny.cz E-resources
- MeSH
- Drosophila melanogaster immunology metabolism MeSH
- Glucans chemistry metabolism MeSH
- Yeasts chemistry MeSH
- Drug Delivery Systems * MeSH
- Macrophages cytology immunology metabolism MeSH
- Drug Carriers chemistry metabolism MeSH
- Drosophila Proteins chemistry metabolism MeSH
- Transcription Factors chemistry metabolism MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
Glucan particles derived from yeast have been recently proposed as potential drug delivery carriers. Here, we demonstrate the potential of glucan particles for protein delivery in vivo, using the insect Drosophila melanogaster as a model organism. By employing genetic tools, we demonstrate the capacity of yeast glucan particles to spread efficiently through the Drosophila body, to enter macrophages and to deliver an active transcription factor protein successfully. Moreover, the glucan particles were nontoxic and induced only minimal immune response. The injection of glucan particles did not impair the ability of Drosophila to fight and survive infection by pathogenic bacteria. From this study, Drosophila emerges as an excellent model to test and develop drug delivery systems based on glucan particles, specifically aimed to regulate macrophages.
Biology Centre CAS Institute of Entomology Branišovská 1160 31 37005 České Budějovice Czech Republic
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc20005848
- 003
- CZ-PrNML
- 005
- 20200528093508.0
- 007
- ta
- 008
- 200511s2019 xxk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1039/c9bm00539k $2 doi
- 035 __
- $a (PubMed)31565713
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxk
- 100 1_
- $a Bajgar, Adam $u University of South Bohemia, Faculty of Sciences, Department of Molecular Biology and Genetics, Branišovska 1160/31, 37005 České Budějovice, Czech Republic and University of Chemistry and Technology Prague, Department of Chemical Engineering, Technická 3, 166 28 Prague, Czech Republic. Frantisek.Stepanek@vscht.cz.
- 245 10
- $a Yeast glucan particles enable intracellular protein delivery in Drosophila without compromising the immune system / $c A. Bajgar, I. Saloň, G. Krejčová, T. DoleŽal, M. Jindra, F. Štěpánek,
- 520 9_
- $a Glucan particles derived from yeast have been recently proposed as potential drug delivery carriers. Here, we demonstrate the potential of glucan particles for protein delivery in vivo, using the insect Drosophila melanogaster as a model organism. By employing genetic tools, we demonstrate the capacity of yeast glucan particles to spread efficiently through the Drosophila body, to enter macrophages and to deliver an active transcription factor protein successfully. Moreover, the glucan particles were nontoxic and induced only minimal immune response. The injection of glucan particles did not impair the ability of Drosophila to fight and survive infection by pathogenic bacteria. From this study, Drosophila emerges as an excellent model to test and develop drug delivery systems based on glucan particles, specifically aimed to regulate macrophages.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a proteiny Drosophily $x chemie $x metabolismus $7 D029721
- 650 _2
- $a Drosophila melanogaster $x imunologie $x metabolismus $7 D004331
- 650 _2
- $a nosiče léků $x chemie $x metabolismus $7 D004337
- 650 12
- $a lékové transportní systémy $7 D016503
- 650 _2
- $a glukany $x chemie $x metabolismus $7 D005936
- 650 _2
- $a makrofágy $x cytologie $x imunologie $x metabolismus $7 D008264
- 650 _2
- $a transkripční faktory $x chemie $x metabolismus $7 D014157
- 650 _2
- $a kvasinky $x chemie $7 D015003
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Saloň, Ivan $u University of Chemistry and Technology Prague, Department of Chemical Engineering, Technická 3, 166 28 Prague, Czech Republic. Frantisek.Stepanek@vscht.cz.
- 700 1_
- $a Krejčová, Gabriela $u University of South Bohemia, Faculty of Sciences, Department of Molecular Biology and Genetics, Branišovska 1160/31, 37005 České Budějovice, Czech Republic.
- 700 1_
- $a DoleŽal, Tomáš $u University of South Bohemia, Faculty of Sciences, Department of Molecular Biology and Genetics, Branišovska 1160/31, 37005 České Budějovice, Czech Republic.
- 700 1_
- $a Jindra, Marek $u Biology Centre CAS, Institute of Entomology, Branišovská 1160/31, 37005 České Budějovice, Czech Republic.
- 700 1_
- $a Štěpánek, František $u University of Chemistry and Technology Prague, Department of Chemical Engineering, Technická 3, 166 28 Prague, Czech Republic. Frantisek.Stepanek@vscht.cz.
- 773 0_
- $w MED00191571 $t Biomaterials science $x 2047-4849 $g Roč. 7, č. 11 (2019), s. 4708-4719
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/31565713 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20200511 $b ABA008
- 991 __
- $a 20200528093505 $b ABA008
- 999 __
- $a ok $b bmc $g 1524706 $s 1095904
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2019 $b 7 $c 11 $d 4708-4719 $e 20190930 $i 2047-4849 $m Biomaterials science $n Biomater Sci $x MED00191571
- GRA __
- $a NV16-27522A $p MZ0
- LZP __
- $a Pubmed-20200511