Brief Article
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World J Gastroenterol. Feb 28, 2011; 17(8): 1026-1029
Published online Feb 28, 2011. doi: 10.3748/wjg.v17.i8.1026
Subcellular distribution of nitric oxide synthase isoforms in the rat duodenum
Petra Talapka, Nikolett Bódi, Izabella Battonyai, Éva Fekete, Mária Bagyánszki
Petra Talapka, Nikolett Bódi, Izabella Battonyai, Éva Fekete, Mária Bagyánszki, Department of Physiology, Anatomy and Neuroscience, University of Szeged, 6726 Szeged, Hungary
Author contributions: Talapka P, Bódi N and Battonyai I contributed equally to this work; Fekete É and Bagyánszki M designed and performed the research; Bódi N and Bagyánszki M analyzed the data; Bódi N, Fekete É and Bagyánszki M wrote the paper.
Supported by Hungarian National Grant Agency, Grant#F46201 to Bagyánszki M
Correspondence to: Mária Bagyánszki, PhD, Lecturer in Zoology, Department of Physiology, Anatomy and Neuroscience, University of Szeged, 6726 Szeged, Hungary. bmarcsi@bio.u-szeged.hu
Telephone: +36-62-544123 Fax: +36-62-544291
Received: September 2, 2010
Revised: November 3, 2010
Accepted: November 10, 2010
Published online: February 28, 2011
Abstract

AIM: To study the cell-type specific subcellular distribution of the three isoforms of nitric oxide synthase (NOS) in the rat duodenum.

METHODS: Postembedding immunoelectronmicroscopy was performed, in which primary antibodies for neuronal NOS (nNOS), endothelial NOS (eNOS), and inducible NOS (iNOS), were visualized with protein A-gold-conjugated secondary antibodies. Stained ultrathin sections were examined and photographed with a Philips CM10 electron microscope equipped with a MEGAVIEW II camera. The specificity of the immunoreaction in all cases was assessed by omitting the primary antibodies in the labeling protocol and incubating the sections only in the protein A-gold conjugated secondary antibodies.

RESULTS: Postembedding immunoelectronmicroscopy revealed the presence of nNOS, eNOS, and iNOS immunoreactivity in the myenteric neurons, the enteric smooth muscle cells, and the endothelium of capillaries running in the vicinity of the myenteric plexus of the rat duodenum. The cell type-specific distributions of the immunogold particles labeling the three different NOS isozymes were revealed. In the control experiments, in which the primary antiserum was omitted, virtually no postembedding gold particles were observed.

CONCLUSION: This postembedding immunoelectronmicroscopic study provided the first evidence of cell-type-specific differences in the subcellular distributions of NOS isoforms.

Keywords: Postembedding immunoelectronmicroscopy, Subcellular distribution, Neuronal nitric oxide synthase, Endothelial nitric oxide synthase, Inducible nitric oxide synthase