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
[1]   DIFFERENTIAL LAMINAR EXPRESSION OF PARTICULATE AND SOLUBLE GUANYLATE-CYCLASE GENES IN RAT RETINA [J].
AHMAD, I ;
BARNSTABLE, CJ .
EXPERIMENTAL EYE RESEARCH, 1993, 56 (01) :51-62
[2]   NITRIC-OXIDE ACTIVATES GUANYLATE CYCLASE AND INCREASES GUANOSINE 3'-5'-CYCLIC MONOPHOSPHATE LEVELS IN VARIOUS TISSUE PREPARATIONS [J].
ARNOLD, WP ;
MITTAL, CK ;
KATSUKI, S ;
MURAD, F .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (08) :3203-3207
[3]   CGMP IMMUNOCYTOCHEMISTRY IN AORTA, KIDNEY, RETINA AND BRAIN-TISSUES OF THE RAT AFTER PERFUSION WITH NITROPRUSSIDE [J].
BERKELMANS, HS ;
SCHIPPER, J ;
HUDSON, L ;
STEINBUSCH, HWM ;
DEVENTE, J .
HISTOCHEMISTRY, 1989, 93 (02) :143-148
[4]   NITRIC-OXIDE DECREASES [CA2+](I) IN VASCULAR SMOOTH-MUSCLE BY INHIBITION OF THE CALCIUM CURRENT [J].
BLATTER, LA ;
WIER, WG .
CELL CALCIUM, 1994, 15 (02) :122-131
[5]   BASAL NITRIC-OXIDE PRODUCTION IN REGULATION OF COCHLEAR BLOOD-FLOW [J].
BRECHTELSBAUER, PB ;
NUTTALL, AL ;
MILLER, JM .
HEARING RESEARCH, 1994, 77 (1-2) :38-42
[6]   LOCALIZATION OF NITRIC-OXIDE SYNTHASE INDICATING A NEURAL ROLE FOR NITRIC-OXIDE [J].
BREDT, DS ;
HWANG, PM ;
SNYDER, SH .
NATURE, 1990, 347 (6295) :768-770
[7]   NITRIC-OXIDE, A NOVEL NEURONAL MESSENGER [J].
BREDT, DS ;
SNYDER, SH .
NEURON, 1992, 8 (01) :3-11
[8]   IMPLICATIONS OF THE NO/CGMP SYSTEM FOR OLFACTION [J].
BREER, H ;
SHEPHERD, GM .
TRENDS IN NEUROSCIENCES, 1993, 16 (01) :5-9
[9]   NITRIC-OXIDE MEDIATED FORMATION OF CYCLIC-GMP IN THE OLFACTORY SYSTEM [J].
BREER, H ;
KLEMM, T ;
BOEKHOFF, I .
NEUROREPORT, 1992, 3 (11) :1030-1032
[10]  
BURGESS BJ, 1995, ABSTR ASS RES OT, V19, P153