Literature DB >> 3974882

The growth of cochlear fibers and the formation of their synaptic endings in the avian inner ear: a study with the electron microscope.

M C Whitehead, D K Morest.   

Abstract

The developmental sequence of nerve-epithelial cell contacts, leading up to the formation of the mature receptoneuronal synapse, has been studied in the basilar papilla of chick embryos with electron microscopy. The receptor epithelium before innervation, on embryonic days 3-4, consists of a homogeneous population of primitive cells; hair cells and supporting cells cannot be distinguished. During innervation of the epithelium (embryonic days 5-7), the invading peripheral fibers of cochlear ganglion cells penetrate the basal lamina and form nerve-epithelial attachments with the epithelial cell bases. Once within the epithelium some fibers turn and spread in the transverse dimension across the basilar papilla through channels formed between the basal epithelial processes. Subsequently, nerve-epithelial attachments are observed more superficially within the epithelium. Hair cells and supporting cells differentiate during early synaptogenesis (embryonic days 8-9). Receptoneural synapses, possibly derived from the nerve-epithelial attachments formed during the innervation stage, are first seen during this period. They are characterized by symmetrical or asymmetrical membrane densities, separated by a cleft containing a dense material. At many of these junctions synaptic bodies, as well as dense-cored and coated vesicles, gather in the hair cells. During mid-synaptogenesis (embryonic days 11-13) the hair cells proliferate synaptic bodies, many of which are not located at receptoneural junctions. The preterminal portions of the sensory endings form large swellings, containing flocculent material, endoplasmic reticulum and vesicles. Late in synaptogenesis (embryonic days 15-17) the swellings disappear, while synaptic endings are transformed to foot-shaped terminals. In the hair cells, synaptic bodies not associated with junctions disappear. Efferent synapses are first seen during this period. This sequence of ultrastructural changes, which the developing sensory nerve endings and their target cells undergo in parallel, can be correlated with observations of Golgi preparations from a companion study. These correlations suggest that the innervation of the cochlea involves the following developmental processes. Initially the peripheral fibers of the ganglion cells grow directly toward the otocyst in fascicles. Having reached the base of the primitive receptor epithelium, the axonal endings, including some with growth cones, encounter a barrier in the basal lamina. When they enter some of the fibers attach to the basal end-feet of the primitive epithelial cells.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1985        PMID: 3974882     DOI: 10.1016/0306-4522(85)90178-2

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  18 in total

1.  Primordial rhythmic bursting in embryonic cochlear ganglion cells.

Authors:  T A Jones; S M Jones; K C Paggett
Journal:  J Neurosci       Date:  2001-10-15       Impact factor: 6.167

2.  Ganglion formation from the otic placode and the otic crest in the chick embryo: mitosis, migration, and the basal lamina.

Authors:  S G Hemond; D K Morest
Journal:  Anat Embryol (Berl)       Date:  1991

3.  Regeneration of cochlear efferent nerve terminals after gentamycin damage.

Authors:  A K Hennig; D A Cotanche
Journal:  J Neurosci       Date:  1998-05-01       Impact factor: 6.167

Review 4.  The Diversity of Spine Synapses in Animals.

Authors:  Ronald S Petralia; Ya-Xian Wang; Mark P Mattson; Pamela J Yao
Journal:  Neuromolecular Med       Date:  2016-05-26       Impact factor: 3.843

5.  Innervation of taste buds revealed with Brainbow-labeling in mouse.

Authors:  Faisal N Zaidi; Vanessa Cicchini; Daniel Kaufman; Elizabeth Ko; Abraham Ko; Heather Van Tassel; Mark C Whitehead
Journal:  J Anat       Date:  2016-08-01       Impact factor: 2.610

6.  Wnt9a Can Influence Cell Fates and Neural Connectivity across the Radial Axis of the Developing Cochlea.

Authors:  Vidhya Munnamalai; Ulrike J Sienknecht; R Keith Duncan; M Katie Scott; Ankita Thawani; Kristen N Fantetti; Nadia M Atallah; Deborah J Biesemeier; Kuhn H Song; Kirsten Luethy; Eric Traub; Donna M Fekete
Journal:  J Neurosci       Date:  2017-08-14       Impact factor: 6.167

7.  Cellular studies of auditory hair cell regeneration in birds.

Authors:  J S Stone; E W Rubel
Journal:  Proc Natl Acad Sci U S A       Date:  2000-10-24       Impact factor: 11.205

Review 8.  Wnt signaling during cochlear development.

Authors:  Vidhya Munnamalai; Donna M Fekete
Journal:  Semin Cell Dev Biol       Date:  2013-03-30       Impact factor: 7.727

9.  Hair cell differentiation in chick cochlear epithelium after aminoglycoside toxicity: in vivo and in vitro observations.

Authors:  J S Stone; S G Leaño; L P Baker; E W Rubel
Journal:  J Neurosci       Date:  1996-10-01       Impact factor: 6.167

10.  Suppression of the slow K+ current by cholinergic agonists in cultured chick cochlear ganglion neurones.

Authors:  K Yamaguchi; H Ohmori
Journal:  J Physiol       Date:  1993-05       Impact factor: 5.182

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