Literature DB >> 667906

Different types of small granule-containing cells and neurons in the guinea-pig adrenal medulla.

K Unsicker, O Habura-Flüh, U Zwarg.   

Abstract

An electron microscopic, histo- and biochemical study was carried out on the adrenal medulla of newborn and adult guinea-pigs giving special emphasis to small granule-containing (SGC) cells. Adrenaline (A) was the predominating catecholamine (CA) both in newborn (70-90% of total CA) and adult (85-90%) guinea-pig adrenals. In analogy to the biochemical findings electron microscopy revealed a high predominance of A cells, which contained large granular vesicles with an average diameter of 180 nm. Most noradrenaline (NA) storing cells showed granular vesicles of a considerably smaller average diameter (80 nm) and had a higher nuclear-cytoplasmic ratio. These cells were termed SGC-NA cells. NA cells with large granular vesicles (average diameter 170 nm) were extremely rare. Another type of SGC cells contained granular vesicles with cores of low to medium electron-density (SGC-NA-negative cells). Biochemical determinations made it unlikely that these cells contained predominantly dopamine (DA). SGC cells were scarcely innervated by cholinergic nerves. They formed processes, which were found both in the adrenal cortex and medulla contacting blood vessels including sinusoid capillaries, steroid producing cells of the reticularis and fasciculata zone and processes, which were interpreted to belong to medullary nerve cells. Two types of neurons were present in the guinea-pig adrenal medulla, one resembling the principal neurons in sympathetic ganglia, the other, which, principal neurons and SGC cells. In adrenomedullary grafts under the kidney capsule, which were studied three weeks after transplantation, "ordinary" A cells resembled SGC-NA negative cells with respect to their ultramorphology. Processes of transplanted principal neurons showed uptake of 5-hydroxydopamine and, hence, were considered to be adrenergic. Despite the lack of extrinsic nerves to the transplants, few principal neurons received cholinergic synapses, the origin of which is uncertain to date.

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Year:  1978        PMID: 667906     DOI: 10.1007/BF00223124

Source DB:  PubMed          Journal:  Cell Tissue Res        ISSN: 0302-766X            Impact factor:   5.249


  51 in total

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5.  Fine structure and innervation of the avian adrenal glands. II. Cholinergic innervation of adrenal chromaffin cells.

Authors:  K Unsicker
Journal:  Z Zellforsch Mikrosk Anat       Date:  1973-12-06

6.  The ultrastructure and somatic efferent synapses of small granule-containing cells in the superior cervical ganglion.

Authors:  M R Matthews; G Raisman
Journal:  J Anat       Date:  1969-09       Impact factor: 2.610

7.  Electron microscopic evidence for the formation of synapses and synaptoid contacts in adrenal medullary grafts.

Authors:  K Unsicker; U Zwarg; O Habura
Journal:  Brain Res       Date:  1977-01-28       Impact factor: 3.252

8.  [Ultrastructural data on an eventual adrenergic modulation of the rat superior cervical ganglion].

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Journal:  C R Acad Hebd Seances Acad Sci D       Date:  1969-10

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Authors:  J C Torre; J W Surgeon
Journal:  Histochemistry       Date:  1976-10-22

10.  Concomitant changes in formaldehyde-induced fluorescence of dopamine interneurones and in slow inhibitory post-synaptic potentials of the rabbit superior cervical ganglion, induced by stimulation of the preganglionic nerve or by a muscarinic agent.

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Journal:  J Physiol       Date:  1974-03       Impact factor: 5.182

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  17 in total

Review 1.  The chromaffin cell and its development.

Authors:  Klaus Unsicker; Katrin Huber; Günther Schütz; Chaya Kalcheim
Journal:  Neurochem Res       Date:  2005 Jun-Jul       Impact factor: 3.996

2.  Ultrastructural evidence for the development of adrenal medullary grafts in the brain.

Authors:  M Jousselin-Hosaja
Journal:  Exp Brain Res       Date:  1988       Impact factor: 1.972

3.  Immunohistochemical correlation of human adrenal nerve fibres and thoracic dorsal root neurons with special reference to substance P.

Authors:  C Heym; B Braun; Y Shuyi; L Klimaschewski; M Colombo-Benkmann
Journal:  Histochem Cell Biol       Date:  1995-09       Impact factor: 4.304

4.  Catecholamine-storing cells in the adrenal medulla of the pre- and postnatal rat. Acetylcholinesterase as a means for early discrimination of cell types.

Authors:  T J Millar; K Unsicker
Journal:  Cell Tissue Res       Date:  1981       Impact factor: 5.249

5.  Comparative morphology, cytochemistry and innervation of chromaffin tissue in vertebrates.

Authors:  D W Scheuermann
Journal:  J Anat       Date:  1993-10       Impact factor: 2.610

Review 6.  Morphological aspects of chromaffin tissue: the differential fixation of adrenaline and noradrenaline.

Authors:  S Kobayashi; R E Coupland
Journal:  J Anat       Date:  1993-10       Impact factor: 2.610

7.  Differentiation and transdifferentiation of adrenal chromaffin cells of the guinea pig. III. Transplants under the kidney capsule.

Authors:  K Unsicker; U Zwarg; O Habura-Flüh
Journal:  Cell Tissue Res       Date:  1983       Impact factor: 5.249

8.  Ultrastructural changes in adrenaline- and SGC-cells after morphine coincide with alterations of adrenaline and dopamine levels.

Authors:  A Thureson-Klein; S Harless; R Klein
Journal:  Cell Tissue Res       Date:  1984       Impact factor: 5.249

9.  Differentiation and transdifferentiation of adrenal chromaffin cells of the guinea pig. II. Adrenal medullary explants grown in tissue culture.

Authors:  K Unsicker
Journal:  Cell Tissue Res       Date:  1981       Impact factor: 5.249

Review 10.  Signals and switches in Mammalian neural crest cell differentiation.

Authors:  Shachi Bhatt; Raul Diaz; Paul A Trainor
Journal:  Cold Spring Harb Perspect Biol       Date:  2013-02-01       Impact factor: 10.005

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