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Cellular expression of Noc2, a Rab effector protein, in endocrine and exocrine tissues in the mouse.

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Please use this identifier to cite or link to this item:http://hdl.handle.net/2115/17155

Title: Cellular expression of Noc2, a Rab effector protein, in endocrine and exocrine tissues in the mouse.
Authors: Teramae, Hiroki Browse this author
Fujimoto, Wakako Browse this author
Seino, Susumu Browse this author
Iwanaga, Toshihiko Browse this author →KAKEN DB
Keywords: Rab
Noc2
Endocrine cell
Exocrine cell
Immunohistochemistry
Issue Date: Jan-2007
Publisher: Springer
Journal Title: Histochemistry and Cell Biology
Volume: 127
Issue: 1
Start Page: 1
End Page: 11
Publisher DOI: 10.1007/s00418-006-0207-0
PMID: 16835753
Abstract: Noc2 is a Rab effector which participates in regulated exocytosis. It is expressed abundantly in endocrine cells but at low levels in exocrine tissues. Noc2-deficient mice, however, exhibit marked accumulation of secretory granules in exocrine cells rather than endocrine cells. In the present study, we investigated localization of Noc2 immunohistochemically in various endocrine and exocrine tissues in normal mice. Western blotting detected a Noc2-immunoreactive band of 38 kDa in isolated pancreatic islets, the adrenal gland, pituitary gland, and thyroid gland. Immunostaining for Noc2 labeled endocrine cells in the adrenal medulla and adenohypophysis, pancreatic islet cells, thyroid parafollicular cells, and gut endocrine cells, supporting the notion that Noc2 is a Rab effector protein shared by amine/peptide-secreting endocrine cells. Besides endocrine tissues, granular ducts in salivary glands contained Noc2. Although immunostaining failed to detect Noc2 in acinar cells of all exocrine glands examined, reverse transcriptase-polymerase chain reaction analysis detected the mRNA expression in exocrine pancreas. Ultrastructurally, Noc2 immunoreactivity was associated with the limiting membrane of granules in both pancreatic endocrine and salivary duct exocrine cells. The cellular and subcellular localizations of Noc2 should yield key information on its functional significance as well as account for the phenotype in Noc2-deficient mice.
Rights: The original publication is available at www.springerlink.com
Type: article (author version)
URI: http://hdl.handle.net/2115/17155
Appears in Collections:医学院・医学研究院 (Graduate School of Medicine / Faculty of Medicine) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 岩永 敏彦

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