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Updated: Aug 7, 2026

In-depth Physiological Analysis of Defined Cell Populations in Acute Tissue Slices of the Mouse Vomeronasal Organ
Published on: September 10, 2016
Cellular expression of Noc2, a Rab effector protein, in endocrine and exocrine tissues in the mouse
Hiroki Teramae1, Wakako Fujimoto, Susumu Seino
1Laboratory of Histology and Cytology, Graduate School of Medicine, Hokkaido University, Kita-15 Nishi-7, Sapporo 060-8638, Japan.
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.
Insights
Noc2 protein is found in various endocrine cells and salivary gland ducts, crucial for secretory granule regulation. Its localization helps explain why Noc2-deficient mice accumulate granules in exocrine tissues.
Area of Science:
- Cell Biology
- Endocrinology
- Molecular Biology
Background:
- Noc2 is a Rab effector involved in regulated exocytosis.
- It is abundant in endocrine cells but scarce in exocrine tissues.
- Noc2 deficiency causes secretory granule accumulation in exocrine cells.
Purpose of the Study:
- To investigate the cellular and subcellular localization of Noc2 in various mouse tissues.
- To understand Noc2's role in both endocrine and exocrine secretion.
- To correlate Noc2 localization with the phenotype observed in Noc2-deficient mice.
Main Methods:
- Immunohistochemistry on various endocrine and exocrine tissues.
- Western blotting to detect Noc2 protein.
- Reverse transcriptase-polymerase chain reaction (RT-PCR) for mRNA expression.
- Ultrastructural analysis of Noc2 localization.
Main Results:
- Noc2 protein was detected in pancreatic islets, adrenal medulla, pituitary, thyroid, and gut endocrine cells.
- Noc2 was also found in granular ducts of salivary glands.
- While not detected by immunostaining in exocrine acinar cells, Noc2 mRNA was present in the exocrine pancreas.
- Ultrastructural analysis showed Noc2 associated with granule membranes in both endocrine and exocrine cells.
Conclusions:
- Noc2 is a Rab effector protein found in amine/peptide-secreting endocrine cells and salivary gland ducts.
- Its localization on granule membranes suggests a role in secretory granule trafficking and exocytosis.
- Understanding Noc2's distribution provides insights into its function and the pathogenesis of Noc2 deficiency.
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