Detail
Článek
Článek online
FT
Medvik - BMČ
  • Je něco špatně v tomto záznamu ?

CD200/CD200R paired potent inhibitory molecules regulating immune and inflammatory responses part I, CD200/CD200R structure, activation, and function

Drahomíra Holmannová, Martina Koláčková, Kateřina Kondělková, Pavel Kuneš, Jan Krejsek, Ctirad Andrýs

. 2012 ; 55 (1) : 12-17.

Jazyk angličtina Země Česko Médium elektronický zdroj

Typ dokumentu přehledy, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc12017003

CD200/CD200R are highly conserved type I paired membrane glycoproteins that belong to the Ig superfamily containing a two immunoglobulin‑like domain (V, C). CD200 is broadly distributed in a variety of cell types, whereas CD200R is primarily expressed in myeloid and lymphoid cells. They fulfill multiple functions in regulating inflammation. The interaction between CD200/CD200R results in activation of the intracellular inhibitory pathway with RasGAP recruitment and thus contributes to effector cell inhibition. It was confirmed that the CD200R activation stimulates the differentiation of T cells to the Treg subset, upregulates indoleamine 2,3‑dioxygenase activity, modulates cytokine environment from a Th1 to a Th2 pattern, and facilitates an antiinflammatory IL‑10 and TGF‑β synthesis. CD200/CD200R are required for maintaining self‑tolerance. Many studies have demonstrated the importance of CD200 in controlling autoimmunity, inflammation, the development and spread of cancer, hypersensitivity, and spontaneous fetal loss.

CD200/CD200R paired potent inhibitory molecules regulating immune and inflammatory responses [elektronický zdroj]. part I, CD200/CD200R structure, activation, and function /

CD200/CD200R structure, activation, and function

Citace poskytuje Crossref.org

Obsahuje 2 tabulky

Bibliografie atd.

Literatura

000      
00000naa a2200000 a 4500
001      
bmc12017003
003      
CZ-PrNML
005      
20120719102339.0
007      
cr|cn|
008      
120531s2012 xr fs 000 0eng||
009      
eAR
024    7_
$a 10.14712/18059694.2015.68 $2 doi
035    __
$a (PubMed)22696929
040    __
$a ABA008 $d ABA008 $e AACR2 $b cze
041    0_
$a eng
044    __
$a xr
100    1_
$a Holmannová, Dráža. $7 mzk2007411153 $u Charles University in Prague, Faculty of Medicine and University Hospital Hradec Králové, Department of Clinical Immunology and Allergology
245    10
$a CD200/CD200R paired potent inhibitory molecules regulating immune and inflammatory responses $h [elektronický zdroj]. $n part I, $p CD200/CD200R structure, activation, and function / $c Drahomíra Holmannová, Martina Koláčková, Kateřina Kondělková, Pavel Kuneš, Jan Krejsek, Ctirad Andrýs
246    30
$a CD200/CD200R structure, activation, and function
500    __
$a Obsahuje 2 tabulky
504    __
$a Literatura $b 46
520    3_
$a CD200/CD200R are highly conserved type I paired membrane glycoproteins that belong to the Ig superfamily containing a two immunoglobulin‑like domain (V, C). CD200 is broadly distributed in a variety of cell types, whereas CD200R is primarily expressed in myeloid and lymphoid cells. They fulfill multiple functions in regulating inflammation. The interaction between CD200/CD200R results in activation of the intracellular inhibitory pathway with RasGAP recruitment and thus contributes to effector cell inhibition. It was confirmed that the CD200R activation stimulates the differentiation of T cells to the Treg subset, upregulates indoleamine 2,3‑dioxygenase activity, modulates cytokine environment from a Th1 to a Th2 pattern, and facilitates an antiinflammatory IL‑10 and TGF‑β synthesis. CD200/CD200R are required for maintaining self‑tolerance. Many studies have demonstrated the importance of CD200 in controlling autoimmunity, inflammation, the development and spread of cancer, hypersensitivity, and spontaneous fetal loss.
650    02
$a zvířata $7 D000818
650    02
$a CD antigeny $x fyziologie $7 D015703
650    02
$a antigeny povrchové $x fyziologie $7 D000954
650    02
$a lidé $7 D006801
650    02
$a imunita $x fyziologie $7 D007109
650    02
$a zánět $x patofyziologie $7 D007249
650    02
$a receptory buněčného povrchu $x fyziologie $7 D011956
650    02
$a signální transdukce $7 D015398
655    _2
$a přehledy $7 D016454
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Koláčková, Martina. $7 _BN000863 $u Charles University in Prague, Faculty of Medicine and University Hospital Hradec Králové, Department of Clinical Immunology and Allergology
700    1_
$a Kondělková, Kateřina. $7 _AN048795 $u Charles University in Prague, Faculty of Medicine and University Hospital Hradec Králové, Department of Clinical Immunology and Allergology
700    1_
$a Kuneš, Pavel $7 xx0082993 $u Charles University in Prague, Faculty of Medicine and University Hospital Hradec Králové, Department of Cardiac Surgery
700    1_
$a Krejsek, Jan, $d 1958- $7 nlk19990073429 $u Charles University in Prague, Faculty of Medicine and University Hospital Hradec Králové, Department of Clinical Immunology and Allergology
700    1_
$a Andrýs, Ctirad, $d 1962- $7 mzk2008430528 $u Charles University in Prague, Faculty of Medicine and University Hospital Hradec Králové, Department of Clinical Immunology and Allergology
773    0_
$t Acta medica (Hradec Králové) $x 1211-4286 $g Roč. 55, č. 1 (2012), s. 12-17 $w MED00010947
856    41
$u https://actamedica.lfhk.cuni.cz/media/pdf/am_2012055010012.pdf $y plný text volně přístupný
910    __
$a ABA008 $b A 3077 $c 1072 $y 2
990    __
$a 20120531144731 $b ABA008
991    __
$a 20120719102253 $b ABA008
999    __
$a ok $b bmc $g 910870 $s 774164
BAS    __
$a 3 $a 4
BMC    __
$a 2012 $b 55 $c 1 $d 12-17 $i 1211-4286 $m Acta Medica $n Acta Med. (Hradec Král.) $x MED00010947
LZP    __
$a 2012-10/mkme

Najít záznam

Citační ukazatele

Pouze přihlášení uživatelé

Možnosti archivace

Nahrávání dat ...