Literature DB >> 3189195

Innervation of the C cells of chicken ultimobranchial glands studied by immunohistochemistry, fluorescence microscopy, and electron microscopy.

Y Kameda1, K Okamoto, M Ito, T Tagawa.   

Abstract

Innervation of the ultimobranchial glands in the chicken was investigated by immunohistochemistry, fluorescence microscopy and electron microscopy. The nerve fibers distributed in ultimobranchial glands were clearly visualized by immunoperoxidase staining with antiserum to neurofilament triplet proteins (200K-, 150K- and 68K-dalton) extracted from chicken peripheral nerves. The ultimobranchial glands received numerous nerve fibers originating from both the recurrent laryngeal nerves and direct vagal branches. The left and right sides of the ultimobranchial region were asymmetrical. The left ultimobranchial gland had intimate contact with the vagus nerve trunk, especially with the distal vagal ganglion, but was somewhat separated from the recurrent nerve. The right gland touched the recurrent nerve, the medial edge being frequently penetrated by the nerve, but the gland was separated from the vagal trunk. The left gland was innervated mainly by the branches from the distal vagal ganglion, whereas the right gland received mostly the branches from the recurrent nerve. The carotid body was located cranially near to the ultimobranchial gland. Large nerve bundles in the ultimobranchial gland ran toward and entered into the carotid body. By fluorescence microscopy, nerve fibers in ultimobranchial glands were observed associated with blood vessels. Only a few fluorescent nerve fibers were present in close proximity to C cell groups; the C cells of ultimobranchial glands may receive very few adrenergic sympathetic fibers. By electron microscopy, numerous axons ensheathed with Schwann cell cytoplasm were in close contact with the surfaces of C cells. In addition, naked axons regarded as axon terminals or "en passant" synapses came into direct contact with C cells. The morphology of these axon terminals and synaptic endings suggest that ultimobranchial C cells of chickens are supplied mainly with cholinergic efferent type fibers. In the region where large nerve bundles and complex ramifications of nerve fibers were present, Schwann cell perikarya investing the axons were closely juxtaposed with C cells; long cytoplasmic processes of Schwann cells encompassed large portions of the cell surface. All of these features suggest that C-cell activity, i.e., secretion of hormones and catecholamines, may be regulated by nerve stimuli.

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Year:  1988        PMID: 3189195     DOI: 10.1002/aja.1001820407

Source DB:  PubMed          Journal:  Am J Anat        ISSN: 0002-9106


  9 in total

Review 1.  Comparative morphological and molecular studies on the oxygen-chemoreceptive cells in the carotid body and fish gills.

Authors:  Yoko Kameda
Journal:  Cell Tissue Res       Date:  2021-04-14       Impact factor: 5.249

2.  Electron microscopic study on the development of the chicken ultimobranchial glands, with special reference to innervation of C cells.

Authors:  Y Kameda
Journal:  Anat Embryol (Berl)       Date:  1993-12

3.  Ontogeny of the carotid body and glomus cells distributed in the wall of the common carotid artery and its branches in the chicken.

Authors:  Y Kameda
Journal:  Cell Tissue Res       Date:  1990-09       Impact factor: 5.249

4.  Localization of nitrergic neuronal and non-neuronal cells in the ultimobranchial glands of the chicken.

Authors:  S M Ali; A S Chan; S K Leong
Journal:  Anat Embryol (Berl)       Date:  1996-02

5.  Distribution of CGRP-, somatostatin-, galanin-, VIP-, and substance P-immunoreactive nerve fibers in the chicken carotid body.

Authors:  Y Kameda
Journal:  Cell Tissue Res       Date:  1989-09       Impact factor: 5.249

6.  Innervation of the chicken parathyroid glands: immunohistochemical study with the TuJ1, galanin, VIP, substance P, CGRP and tyrosine hydroxylase antibodies.

Authors:  C Egawa; Y Kameda
Journal:  Anat Embryol (Berl)       Date:  1995-05

7.  Accessory carotid body within the parathyroid gland III of the chicken.

Authors:  Y Yamatsu; Y Kameda
Journal:  Histochem Cell Biol       Date:  1995-03       Impact factor: 4.304

8.  Distribution and ontogeny of chromogranin A and tyrosine hydroxylase in the carotid body and glomus cells located in the wall of the common carotid artery and its branches in the chicken.

Authors:  Y Kameda; T Amano; T Tagawa
Journal:  Histochemistry       Date:  1990

9.  Immuno-electron-microscopic localization of enkephalin in the secretory granules of C cells in the chicken ultimobranchial glands.

Authors:  Y Kameda; C Hirota; M Murakami
Journal:  Cell Tissue Res       Date:  1993-11       Impact factor: 5.249

  9 in total

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