GENERATION OF XENOPSIN-RELATED PEPTIDES FROM TISSUE PRECURSORS BY MEDIA CONDITIONED BY ENDOTOXIN-STIMULATED RAT PERITONEAL-MACROPHAGES

被引:7
作者
COCHRANE, DE [1 ]
CARRAWAY, RE [1 ]
BOUCHER, W [1 ]
机构
[1] UNIV MASSACHUSETTS,SCH MED,DEPT PHYSIOL,WORCESTER,MA 01655
关键词
D O I
10.1007/BF00917354
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Incubation of media conditioned by endotoxin-stimulated rat peritoneal macrophages generates immunoreactive xenopsin (iXP) when incubated with acid extracts of various tissues of the rat. The generation of iXP, as measured by specific radioimmunoassay and confirmed by HPLC analysis, increased as the length of the incubation period increased and was inhibited by pepstatin, prior boiling of the conditioned media, or by omitting either the tissue extract or the conditioned media. The pH optimum for the generation of iXP was 3.0. The generated iXP showed biological activity in that stimulated histamine secretion from isolated rat mast cells and this secretory response was prevented by metabolically poisoning the cells. In addition, the generated iXP stimulated contraction of the isolated guinea pig ileum. In this regard, it was similar to neurotensin (NT). Tissue precursor levels for iXP, as measured by this system of generation, were highest in kidney, liver, and skin and lowest in skeletal muscle and plasma. These results suggest to us that during the inflammatory response, the NT-related peptide, xenopsin, can be generated from tissue precursor(s) by enzymes secreted by invading macrophages. The generated XP may then affect the participating cells of inflammation.
引用
收藏
页码:381 / 390
页数:10
相关论文
共 27 条
[1]   COMPARATIVE STUDIES OF XENOPSIN AND NEUROTENSIN ON SOME BIOLOGICAL-ACTIVITIES [J].
ARAKI, K ;
TACHIBANA, S ;
KATO, Y ;
TAJIMA, T .
YAKUGAKU ZASSHI-JOURNAL OF THE PHARMACEUTICAL SOCIETY OF JAPAN, 1979, 99 (05) :466-470
[2]  
ARAKI K, 1975, CHEM PHARM BULL, V23, P132
[3]   CATHEPSIN-D ACTIVITY IN HUMAN PERIPHERAL-BLOOD MONONUCLEAR LEUKOCYTES [J].
BEVER, CT ;
MORGAN, KD ;
WHITAKER, JN .
INFLAMMATION, 1989, 13 (03) :309-316
[4]   AMPHIBIAN NEUROTENSIN (NT) IS NOT XENOPSIN (XP) - DUAL PRESENCE OF NT-LIKE AND XP-LIKE PEPTIDES IN VARIOUS AMPHIBIA [J].
CARRAWAY, R ;
RUANE, SE ;
FEURLE, GE ;
TAYLOR, S .
ENDOCRINOLOGY, 1982, 110 (04) :1094-1101
[5]   NEUROTENSIN STIMULATES EXOCYTOTIC HISTAMINE-SECRETION FROM RAT MAST-CELLS AND ELEVATES PLASMA HISTAMINE LEVELS [J].
CARRAWAY, R ;
COCHRANE, DE ;
LANSMAN, JB ;
LEEMAN, SE ;
PATERSON, BM ;
WELCH, HJ .
JOURNAL OF PHYSIOLOGY-LONDON, 1982, 323 (FEB) :403-&
[6]  
CARRAWAY RE, 1987, J BIOL CHEM, V262, P5968
[7]   XENOPSIN-RELATED PEPTIDE(S) ARE FORMED FROM XENOPSIN PRECURSOR BY LEUKOCYTE PROTEASE(S) AND CATHEPSIN-D [J].
CARRAWAY, RE ;
MITRA, SP ;
MURAKI, K .
PEPTIDES, 1991, 12 (01) :107-112
[8]   ISOLATION AND STRUCTURES OF XENOPSIN-RELATED PEPTIDES FROM RAT STOMACH, LIVER AND BRAIN [J].
CARRAWAY, RE ;
MITRA, SP ;
MURAKI, K .
REGULATORY PEPTIDES, 1990, 29 (2-3) :229-239
[9]   XENOPSIN-RELATED PEPTIDE GENERATED IN AVIAN GASTRIC EXTRACTS [J].
CARRAWAY, RE ;
COCHRANE, DE ;
MITRA, SP .
REGULATORY PEPTIDES, 1988, 22 (04) :303-314
[10]  
CARRAWAY RE, 1989, J IMMUNOL, V143, P1680