Further studies of the secretory process in hypothalamo-neurohypophysial neurons: an analysis using immunocytochemistry, wheat germ agglutinin-peroxidase, and native peroxidase
- PMID: 6207213
- DOI: 10.1002/cne.902280203
Further studies of the secretory process in hypothalamo-neurohypophysial neurons: an analysis using immunocytochemistry, wheat germ agglutinin-peroxidase, and native peroxidase
Abstract
The axonal endoplasmic reticulum (ER) and synaptic-like (micro)vesicles within axon terminals of the neurohypophysis and their contribution to the secretory process in hypothalamo-neurohypophysial neurons have been investigated cytochemically in normal mice and in mice given 2% salt water to drink for stimulation of hormone synthesis in and release from these neurons. Cytochemical techniques included the peroxidase-antiperoxidase (PAP) immunocytochemical method for localization of neurophysin, wheat germ agglutinin-horseradish peroxidase (WGA-HRP) as a tracer for the anterograde axonal transport of membrane from within the perikaryon, and blood-borne native horseradish peroxidase (HRP) as a tracer for internalized axon terminal membrane. The primary antiserum employed was directed against neurophysins I and II, the carrier proteins for the peptide hormones oxytocin and vasopressin, respectively. PAP reaction product was observed over neurosecretory granules but never over the endoplasmic reticulum, microvesicles or other organelles in axons and terminals of the neurohypophysis. WGA-HRP was delivered extracellularly to cell bodies of paraventricular neurons by cerebral ventriculocisternal perfusion. Internalized perikaryal surface membrane tagged with WGA-HRP was recycled through the innermost Golgi saccule (GERL) from which neurosecretory granules were formed. The anterograde axonal transport of membrane-bound WGA-HRP was manifested within the neurosecretory granules; WGA-HRP did not label the axonal reticulum or terminal microvesicles in the neurohypophysis. Blood-borne native HRP endocytosed into neurohypophysial terminals was associated with a plethora of microvesicles measuring 40-70 nm in diameter and vacuoles similar in size to the 100-300-nm-wide neurosecretory granules. The microvesicles contributed to the formation of numerous vacuoles. The internalization of axon terminal membrane as microvesicles incorporating HRP was quantitatively greater than vacuoles in both salt-stressed and control mice. The results suggest that in the hypothalamo-neurohypophysial system of the mouse the axonal ER and terminal microvesicles are not involved in the transport, storage, and exocytosis of neurosecretory material and perhaps other molecules processed through the innermost Golgi saccule. Nevertheless, a prominent population of the microvesicles within axon terminals of the neurohypophysis does participate in the secretory process. These vesicles are involved directly in the internalization of the terminal surface membrane subsequent to release of secretory granule content.(ABSTRACT TRUNCATED AT 400 WORDS)
Similar articles
-
Endocytic and exocytic pathways of the neuronal secretory process and trans-synaptic transfer of wheat germ agglutinin-horseradish peroxidase in vivo.J Comp Neurol. 1985 Dec 22;242(4):632-50. doi: 10.1002/cne.902420410. J Comp Neurol. 1985. PMID: 2418083
-
Neuronal transport of acid hydrolases and peroxidase within the lysosomal system or organelles: involvement of agranular reticulum-like cisterns.J Comp Neurol. 1980 Apr 1;190(3):519-32. doi: 10.1002/cne.901900308. J Comp Neurol. 1980. PMID: 6156186
-
The neuronal endoplasmic reticulum: its cytochemistry and contribution to the endomembrane system. II. Axons and terminals.J Comp Neurol. 1984 Dec 1;230(2):231-48. doi: 10.1002/cne.902300208. J Comp Neurol. 1984. PMID: 6210310
-
Analysis of neuronal networks: a review of techniques for labeling axonal projections.J Electron Microsc Tech. 1990 Aug;15(4):322-31. doi: 10.1002/jemt.1060150403. J Electron Microsc Tech. 1990. PMID: 1697336 Review.
-
A review on neurosecretory granules: their contents and mechanisms of release.Ann N Y Acad Sci. 1975 Feb 21;248:184-201. doi: 10.1111/j.1749-6632.1975.tb34185.x. Ann N Y Acad Sci. 1975. PMID: 1091194 Review.
Cited by
-
Avoiding off-target effects in electrical stimulation of the cervical vagus nerve: Neuroanatomical tracing techniques to study fascicular anatomy of the vagus nerve.J Neurosci Methods. 2019 Sep 1;325:108325. doi: 10.1016/j.jneumeth.2019.108325. Epub 2019 Jun 28. J Neurosci Methods. 2019. PMID: 31260728 Free PMC article. Review.
-
Membrane routing during exocytosis and endocytosis in neuroendocrine neurones and endocrine cells: use of colloidal gold particles and immunocytochemical discrimination of membrane compartments.Cell Tissue Res. 1991 May;264(2):299-316. doi: 10.1007/BF00313967. Cell Tissue Res. 1991. PMID: 1715242
-
Transneuronal transport of peroxidase-conjugated wheat germ agglutinin (WGA-HRP) from the olfactory epithelium to the brain of the adult rat.Exp Brain Res. 1986;63(3):461-73. doi: 10.1007/BF00237470. Exp Brain Res. 1986. PMID: 3758265
-
Transcytosis of macromolecules through the blood-brain barrier: a cell biological perspective and critical appraisal.Acta Neuropathol. 1989;79(2):117-28. doi: 10.1007/BF00294368. Acta Neuropathol. 1989. PMID: 2688350 Review.
-
Protein p38: an integral membrane protein specific for small vesicles of neurons and neuroendocrine cells.J Cell Biol. 1986 Dec;103(6 Pt 1):2511-27. doi: 10.1083/jcb.103.6.2511. J Cell Biol. 1986. PMID: 3097029 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Research Materials