Robert M Douglas, Alice H Chen, Alejandra Iniguez, Juan Wang, Zhengxing Fu, Frank L Powell, Gabriel G Haddad, Hang Yao
{"title":"趋化因子受体样2参与缺血性脑损伤。","authors":"Robert M Douglas, Alice H Chen, Alejandra Iniguez, Juan Wang, Zhengxing Fu, Frank L Powell, Gabriel G Haddad, Hang Yao","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>We examined the role of CCRL2 in ischemic brain injury using both <i>in vitro</i> and <i>in vivo</i> mouse stroke models. The expression of CCRL2 was enhanced at both the RNA and protein levels in cultured brain slices under ischemic conditions. Ischemia-induced cell death was reduced in brain slices derived from CCRL2 knockout (KO) mice in comparison with those from wild type (WT) mice. The infarct volume was smaller and neurological deficits were attenuated in CCRL2 KO mice when compared to WT mice subjected to a transient middle cerebral artery occlusion. Our data suggest that CCRL2 is involved in ischemia-induced brain injury in mice.</p>","PeriodicalId":88544,"journal":{"name":"Journal of experimental stroke & translational medicine","volume":"6 ","pages":"1-6"},"PeriodicalIF":0.0000,"publicationDate":"2013-02-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3705577/pdf/nihms453552.pdf","citationCount":"0","resultStr":"{\"title\":\"Chemokine receptor-like 2 is involved in ischemic brain injury.\",\"authors\":\"Robert M Douglas, Alice H Chen, Alejandra Iniguez, Juan Wang, Zhengxing Fu, Frank L Powell, Gabriel G Haddad, Hang Yao\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>We examined the role of CCRL2 in ischemic brain injury using both <i>in vitro</i> and <i>in vivo</i> mouse stroke models. The expression of CCRL2 was enhanced at both the RNA and protein levels in cultured brain slices under ischemic conditions. Ischemia-induced cell death was reduced in brain slices derived from CCRL2 knockout (KO) mice in comparison with those from wild type (WT) mice. The infarct volume was smaller and neurological deficits were attenuated in CCRL2 KO mice when compared to WT mice subjected to a transient middle cerebral artery occlusion. Our data suggest that CCRL2 is involved in ischemia-induced brain injury in mice.</p>\",\"PeriodicalId\":88544,\"journal\":{\"name\":\"Journal of experimental stroke & translational medicine\",\"volume\":\"6 \",\"pages\":\"1-6\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2013-02-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3705577/pdf/nihms453552.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of experimental stroke & translational medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of experimental stroke & translational medicine","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Chemokine receptor-like 2 is involved in ischemic brain injury.
We examined the role of CCRL2 in ischemic brain injury using both in vitro and in vivo mouse stroke models. The expression of CCRL2 was enhanced at both the RNA and protein levels in cultured brain slices under ischemic conditions. Ischemia-induced cell death was reduced in brain slices derived from CCRL2 knockout (KO) mice in comparison with those from wild type (WT) mice. The infarct volume was smaller and neurological deficits were attenuated in CCRL2 KO mice when compared to WT mice subjected to a transient middle cerebral artery occlusion. Our data suggest that CCRL2 is involved in ischemia-induced brain injury in mice.