-
Something wrong with this record ?
Neuronal Migration Generates New Populations of Neurons That Develop Unique Connections, Physiological Properties and Pathologies
B. Fritzsch, KL. Elliott, G. Pavlinkova, JS. Duncan, MR. Hansen, JM. Kersigo,
Language English Country Switzerland
Document type Journal Article, Review
NLK
Directory of Open Access Journals
from 2013
Free Medical Journals
from 2013
PubMed Central
from 2013
Europe PubMed Central
from 2013
Open Access Digital Library
from 2013-01-01
Open Access Digital Library
from 2013-01-01
ROAD: Directory of Open Access Scholarly Resources
from 2013
- Publication type
- Journal Article MeSH
- Review MeSH
Central nervous system neurons become postmitotic when radial glia cells divide to form neuroblasts. Neuroblasts may migrate away from the ventricle radially along glia fibers, in various directions or even across the midline. We present four cases of unusual migration that are variably connected to either pathology or formation of new populations of neurons with new connectivities. One of the best-known cases of radial migration involves granule cells that migrate from the external granule cell layer along radial Bergman glia fibers to become mature internal granule cells. In various medulloblastoma cases this migration does not occur and transforms the external granule cell layer into a rapidly growing tumor. Among the ocular motor neurons is one unique population that undergoes a contralateral migration and uniquely innervates the superior rectus and levator palpebrae muscles. In humans, a mutation of a single gene ubiquitously expressed in all cells, induces innervation defects only in this unique motor neuron population, leading to inability to elevate eyes or upper eyelids. One of the best-known cases for longitudinal migration is the facial branchial motor (FBM) neurons and the overlapping inner ear efferent population. We describe here molecular cues that are needed for the caudal migration of FBM to segregate these motor neurons from the differently migrating inner ear efferent population. Finally, we describe unusual migration of inner ear spiral ganglion neurons that result in aberrant connections with disruption of frequency presentation. Combined, these data identify unique migratory properties of various neuronal populations that allow them to adopt new connections but also sets them up for unique pathologies.
Department of Biological Sciences Western Michigan University Kalamazoo MI United States
Department of Biology University of Iowa Iowa City IA United States
Department of Otolaryngology University of Iowa Iowa City IA United States
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc19029032
- 003
- CZ-PrNML
- 005
- 20240624150231.0
- 007
- ta
- 008
- 190813e20190424sz f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.3389/fcell.2019.00059 $2 doi
- 035 __
- $a (PubMed)31069224
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a sz
- 100 1_
- $a Fritzsch, Bernd $u Department of Biology, University of Iowa, Iowa City, IA, United States. Department of Otolaryngology, University of Iowa, Iowa City, IA, United States.
- 245 10
- $a Neuronal Migration Generates New Populations of Neurons That Develop Unique Connections, Physiological Properties and Pathologies / $c B. Fritzsch, KL. Elliott, G. Pavlinkova, JS. Duncan, MR. Hansen, JM. Kersigo,
- 520 9_
- $a Central nervous system neurons become postmitotic when radial glia cells divide to form neuroblasts. Neuroblasts may migrate away from the ventricle radially along glia fibers, in various directions or even across the midline. We present four cases of unusual migration that are variably connected to either pathology or formation of new populations of neurons with new connectivities. One of the best-known cases of radial migration involves granule cells that migrate from the external granule cell layer along radial Bergman glia fibers to become mature internal granule cells. In various medulloblastoma cases this migration does not occur and transforms the external granule cell layer into a rapidly growing tumor. Among the ocular motor neurons is one unique population that undergoes a contralateral migration and uniquely innervates the superior rectus and levator palpebrae muscles. In humans, a mutation of a single gene ubiquitously expressed in all cells, induces innervation defects only in this unique motor neuron population, leading to inability to elevate eyes or upper eyelids. One of the best-known cases for longitudinal migration is the facial branchial motor (FBM) neurons and the overlapping inner ear efferent population. We describe here molecular cues that are needed for the caudal migration of FBM to segregate these motor neurons from the differently migrating inner ear efferent population. Finally, we describe unusual migration of inner ear spiral ganglion neurons that result in aberrant connections with disruption of frequency presentation. Combined, these data identify unique migratory properties of various neuronal populations that allow them to adopt new connections but also sets them up for unique pathologies.
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a přehledy $7 D016454
- 700 1_
- $a Elliott, Karen L $u Department of Biology, University of Iowa, Iowa City, IA, United States.
- 700 1_
- $a Pavlínková, Gabriela, $u Institute of Biotechnology ASCR, Vestec, Czechia. $d 1966- $7 xx0319150
- 700 1_
- $a Duncan, Jeremy S $u Department of Biological Sciences, Western Michigan University, Kalamazoo, MI, United States.
- 700 1_
- $a Hansen, Marlan R $u Department of Otolaryngology, University of Iowa, Iowa City, IA, United States.
- 700 1_
- $a Kersigo, Jennifer M $u Department of Biology, University of Iowa, Iowa City, IA, United States.
- 773 0_
- $w MED00186212 $t Frontiers in cell and developmental biology. $x 2296-634X $g Roč. 7 (20190424), s. 59
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/31069224 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20190813 $b ABA008
- 991 __
- $a 20240624150229 $b ABA008
- 999 __
- $a ind $b bmc $g 1434181 $s 1067492
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2019 $b 7 $c - $d 59 $e 20190424 $i 2296-634X $m Frontiers in cell and developmental biology. $n Front Cell Dev Biol $x MED00186212
- LZP __
- $a Pubmed-20190813