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Volumn 167, Issue 11, 2001, Pages 6609-6614

The endogenous opioid spinorphin blocks fMet-Leu-Phe-induced neutrophil chemotaxis by acting as a specific antagonist at the N-formylpeptide receptor subtype FPR

Author keywords

[No Author keywords available]

Indexed keywords

ANGIOTENSIN RECEPTOR; FORMYLMETHIONYLLEUCYLPHENYLALANINE; FORMYLPEPTIDE; HEMORPHIN 4; HEPTAPEPTIDE; OPIATE; RECEPTOR SUBTYPE; SPINORPHIN;

EID: 0035575780     PISSN: 00221767     EISSN: None     Source Type: Journal    
DOI: 10.4049/jimmunol.167.11.6609     Document Type: Article
Times cited : (35)

References (49)
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    • (2000) Peptides , vol.21 , pp. 137
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  • 16
    • 0030910559 scopus 로고    scopus 로고
    • Investigation of inhibition angiotensin-converting enzyme (ACE) activity and opioid activity of two hemorphins, LVV-hemorphin-5 and VV-hemorphin-5, isolated from a defined peptic hydrolysate of bovine hemoglobin
    • (1997) Neuropeptides , vol.31 , pp. 147
    • Zhao, Q.1    Piot, J.M.2
  • 35
    • 0027370126 scopus 로고
    • Species and subtype variants of the N-formyl peptide chemoattractant receptor reveal multiple important functional domains
    • (1993) J. Biol. Chem. , vol.268 , pp. 25395
    • Gao, J.-L.1    Murphy, P.M.2
  • 38
    • 0032841624 scopus 로고    scopus 로고
    • N-formylpeptides induce two distinct concentration optima for mouse neutrophil chemotaxis by differential interaction with two N-formylpeptide receptor (FPR) subtypes: Molecular characterization of FPR2, a second mouse neutrophil FPR
    • (1999) J. Exp. Med. , vol.190 , pp. 741
    • Hartt, J.K.1    Barish, G.2    Murphy, P.M.3    Gao, J.-L.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.