-
Something wrong with this record ?
Adenosine A1, A2a, A2b, and A3 receptors in hematopoiesis. 2. Expression of receptor mRNA in resting and lipopolysaccharide-activated mouse RAW 264.7 macrophages
D. Štreitová, M. Hofer, J. Holá, A. Vacek, M. Pospíšil
Language English Country Czech Republic
NLK
Directory of Open Access Journals
from 1991
Free Medical Journals
from 1998
ProQuest Central
from 2005-01-01
Medline Complete (EBSCOhost)
from 2006-01-01
Nursing & Allied Health Database (ProQuest)
from 2005-01-01
Health & Medicine (ProQuest)
from 2005-01-01
ROAD: Directory of Open Access Scholarly Resources
from 1998
- MeSH
- Macrophage Activation genetics drug effects MeSH
- Cell Line MeSH
- Time Factors MeSH
- Financing, Organized MeSH
- Hematopoiesis genetics drug effects MeSH
- Lipopolysaccharides pharmacology MeSH
- Macrophages metabolism drug effects MeSH
- RNA, Messenger metabolism MeSH
- Mice MeSH
- Polymerase Chain Reaction MeSH
- Receptors, Purinergic P1 genetics drug effects MeSH
- Receptor, Adenosine A1 genetics MeSH
- Receptor, Adenosine A2A genetics MeSH
- Receptor, Adenosine A2B genetics MeSH
- Receptor, Adenosine A3 genetics MeSH
- Gene Expression Regulation MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Animals MeSH
Expression of mRNA for adenosine receptor subtypes A(1), A(2a), A(2b), and A(3) in normal and lipopolysaccharide (LPS)-activated murine RAW 264.7 macrophages has been investigated using the method of quantitative real-time polymerase chain reaction. The results have shown a very low, unquantifiable expression of adenosine A(1) receptor mRNA in both normal and LPS-activated macrophages. The other three adenosine receptor mRNAs have been found to be expressed at various but always quantifiable levels. Activation of the macrophages by LPS induced upregulation of the expression of adenosine receptor A(2a) and A(2b) mRNA, whereas the expression of adenosine receptor A(3) mRNA was downregulated. Unstimulated macrophages exhibited a high expression of the A(2b) adenosine receptor mRNA. The findings are discussed from the point of view of the antiinflammatory and hematopoiesis-stimulating roles of the adenosine receptor signaling.
References provided by Crossref.org
Lit.: 25
- 000
- 00000naa 2200000 a 4500
- 001
- bmc10013144
- 003
- CZ-PrNML
- 005
- 20111210175217.0
- 008
- 100602s2010 xr e eng||
- 009
- AR
- 024 7_
- $a 10.33549/physiolres.931724 $2 doi
- 040 __
- $a ABA008 $b cze $c ABA008 $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Štreitová, Denisa. $7 xx0044358
- 245 10
- $a Adenosine A1, A2a, A2b, and A3 receptors in hematopoiesis. 2. Expression of receptor mRNA in resting and lipopolysaccharide-activated mouse RAW 264.7 macrophages / $c D. Štreitová, M. Hofer, J. Holá, A. Vacek, M. Pospíšil
- 314 __
- $a Institute of Biophysics, v.v.i., Brno hofer@ibp.cz.
- 504 __
- $a Lit.: 25
- 520 9_
- $a Expression of mRNA for adenosine receptor subtypes A(1), A(2a), A(2b), and A(3) in normal and lipopolysaccharide (LPS)-activated murine RAW 264.7 macrophages has been investigated using the method of quantitative real-time polymerase chain reaction. The results have shown a very low, unquantifiable expression of adenosine A(1) receptor mRNA in both normal and LPS-activated macrophages. The other three adenosine receptor mRNAs have been found to be expressed at various but always quantifiable levels. Activation of the macrophages by LPS induced upregulation of the expression of adenosine receptor A(2a) and A(2b) mRNA, whereas the expression of adenosine receptor A(3) mRNA was downregulated. Unstimulated macrophages exhibited a high expression of the A(2b) adenosine receptor mRNA. The findings are discussed from the point of view of the antiinflammatory and hematopoiesis-stimulating roles of the adenosine receptor signaling.
- 650 _2
- $a financování organizované $7 D005381
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a buněčné linie $7 D002460
- 650 _2
- $a regulace genové exprese $7 D005786
- 650 _2
- $a hematopoéza $x genetika $x účinky léků $7 D006410
- 650 _2
- $a lipopolysacharidy $x farmakologie $7 D008070
- 650 _2
- $a aktivace makrofágů $x genetika $x účinky léků $7 D008262
- 650 _2
- $a makrofágy $x metabolismus $x účinky léků $7 D008264
- 650 _2
- $a myši $7 D051379
- 650 _2
- $a polymerázová řetězová reakce $7 D016133
- 650 _2
- $a messenger RNA $x metabolismus $7 D012333
- 650 _2
- $a receptor adenosinový A1 $x genetika $7 D043682
- 650 _2
- $a receptor adenosinový A2A $x genetika $7 D043705
- 650 _2
- $a receptor adenosinový A2B $x genetika $7 D043704
- 650 _2
- $a receptor adenosinový A3 $x genetika $7 D043684
- 650 _2
- $a purinergní receptory P1 $x genetika $x účinky léků $7 D018047
- 650 _2
- $a časové faktory $7 D013997
- 700 1_
- $a Hofer, Michal $7 xx0074123
- 700 1_
- $a Holá, Jiřina $7 xx0074137
- 700 1_
- $a Vacek, Antonín, $d 1929-2009 $7 jk01140948
- 700 1_
- $a Pospíšil, Milan, $d 1929- $7 jk01100711
- 773 0_
- $w MED00003824 $t Physiological research $g Roč. 59, č. 1 (2010), s. 139-144 $x 0862-8408
- 856 41
- $u http://www.biomed.cas.cz/physiolres/pdf/59/59_139.pdf $y plný text volně přístupný
- 910 __
- $a ABA008 $b A 4120 $c 266 $y 8
- 990 __
- $a 20100601135354 $b ABA008
- 991 __
- $a 20101123170257 $b ABA008
- 999 __
- $a ok $b bmc $g 749042 $s 612639
- BAS __
- $a 3
- BMC __
- $a 2010 $b 59 $c 1 $d 139-144 $m Physiological research $x MED00003824
- LZP __
- $a 2010-15/mkme