Localization of soluble guanylate cyclase activity in the guinea pig cochlea suggests involvement in regulation of blood flow and supporting cell physiology

被引:40
作者
Fessenden, JD
Schacht, J
机构
[1] UNIV MICHIGAN,KRESGE HEARING RES INST,ANN ARBOR,MI 48109
[2] UNIV MICHIGAN,DEPT BIOL CHEM,ANN ARBOR,MI 48109
关键词
soluble guanylate cyclase; cochlea; immunohistochemistry; NADPH-diaphorase; cGMP; pericytes; supporting cells; blood flow;
D O I
10.1177/002215549704501008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Although the nitric oxide/cGMP pathway has many important roles in biology, studies of this system in the mammalian cochlea have focused on the first enzyme in the pathway, nitric oxide synthase (NOS). However, characterization of the NO receptor, soluble guanylate cyclase (sGC), is crucial to determine the cells targeted by NO and to develop rational hypotheses of the function of this pathway in auditory processing. In this study we characterized guinea pig cochlear sGC by determining its enzymatic activity and cellular localization. In cytosolic fractions of auditory nerve, lateral wall tissues, and cochlear neuroepithelium, addition of NO donors resulted in three-to 15-fold increases in cGMP formation. NO-stimulated sGC activity was not detected in particulate fractions. We also localized cochlear sGC activity through immunocytochemical detection of NO-stimulated cGMP. sGC activity was detected in Hensen's and Deiters' cells of the organ of Corti, as well as in vascular pericytes surrounding small capillaries in the lateral wall tissues and sensory neuroepithelium. sGC activity was not observed in sensory celis. Using NADPH-diaphorase histochemistry, NOS was localized to pillar cells and nerve fibers underlying hair cells. These results indicate that the NO/cGMP pathway may influence diverse elements of the auditory system, including cochlear blood flow and supporting cell physiology.
引用
收藏
页码:1401 / 1408
页数:8
相关论文
共 49 条
[21]   GUANYLATE CYCLASE AND CYCLIC GUANOSINE MONOPHOSPHATE IN GUINEA-PIG COCHLEA [J].
GUTH, PS ;
STOCKWELL, M .
JOURNAL OF NEUROCHEMISTRY, 1977, 28 (01) :263-265
[22]  
HAEFLIGER IO, 1994, INVEST OPHTH VIS SCI, V35, P991
[23]   ROLE OF VASOCONSTRICTION IN NOISE-INDUCED HEARING LOSS [J].
HAWKINS, JE .
ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY, 1971, 80 (06) :903-&
[24]   COCHLEAR MICROVASCULATURE IN NORMAL AND DAMAGED EARS [J].
HAWKINS, JE ;
JOHNSSON, LG ;
PRESTON, RE .
LARYNGOSCOPE, 1972, 82 (07) :1091-&
[25]  
HIRATA M, 1990, J BIOL CHEM, V265, P1268
[26]   PERICYTES, LIKE VASCULAR SMOOTH-MUSCLE CELLS, ARE IMMUNOCYTOCHEMICALLY POSITIVE FOR CYCLIC GMP-DEPENDENT PROTEIN-KINASE [J].
JOYCE, NC ;
DECAMILLI, P ;
BOYLES, J .
MICROVASCULAR RESEARCH, 1984, 28 (02) :206-219
[27]  
KAMISAKI Y, 1986, J BIOL CHEM, V261, P7236
[28]   NITRIC-OXIDE AS A SIGNAL IN BLOOD-VESSELS [J].
KNOWLES, RG ;
MONCADA, S .
TRENDS IN BIOCHEMICAL SCIENCES, 1992, 17 (10) :399-402
[29]   Electrophysiological and morphological evaluation of the acute ototoxicity of sodium nitroprusside [J].
Kong, WJ ;
Ren, TY ;
Nuttall, AL .
HEARING RESEARCH, 1996, 99 (1-2) :22-30
[30]   SOMATOSTATIN-INDUCED INHIBITION OF NEURONAL CA2+ CURRENT MODULATED BY CGMP-DEPENDENT PROTEIN-KINASE [J].
MERINEY, SD ;
GRAY, DB ;
PILAR, GR .
NATURE, 1994, 369 (6478) :336-339