Literature DB >> 1281492

c-kit receptor and ligand expression in postnatal development of the mouse cerebellum suggests a function for c-kit in inhibitory interneurons.

K Manova1, R F Bachvarova, E J Huang, S Sanchez, S M Pronovost, E Velazquez, B McGuire, P Besmer.   

Abstract

The c-kit receptor and its cognate ligand, KL, are encoded at the white spotting locus (W) and the steel locus (Sl) of the mouse, respectively. Sl and W mutations affect the same cellular targets in melanogenesis, gametogenesis and hematopoiesis during embryonic development and in adult life. c-kit is expressed in cellular targets of W and Sl mutations, whereas KL is expressed in the microenvironment of these targets. c-kit and KL, however, are also expressed in tissues and cell types that are not targets of W and Sl mutations, including the brain. The cerebellum contains a small number of neural cell types whose developmental origins, pathways of migration, and synaptic contacts are known. We have investigated the patterns of expression of the c-kit and KL RNA and protein products in postnatal cerebellar development of the mouse. In the adult cerebellum, c-kit RNA and protein expression was evident in basket, stellate, and Golgi neurons. Most strikingly, the c-kit protein is expressed in the basket cell axons that form "basket" and "pinceau" structures entwining the Purkinje cell soma and the initial segment of the Purkinje cell axon. KL RNA expression was found in Purkinje cells, and the KL protein was detected in Purkinje cell bodies and dendrites. Soluble KL protein was also present in c-kit-expressing basket, stellate, and Golgi cells, presumably as a result of internalization of ligand-receptor complexes. During postnatal development, c-kit and KL RNA and protein expression in Golgi and Purkinje neurons, respectively, was evident by day 0 and persisted subsequently. c-kit expression in basket and stellate cells was detected from their time of birth, starting at day 4. These results suggest a role for the c-kit receptor system in postnatal development of the cerebellum.

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Year:  1992        PMID: 1281492      PMCID: PMC6575762     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  16 in total

1.  The treasury of the commons: making use of public gene expression resources to better characterize the molecular diversity of inhibitory interneurons in the cerebellar cortex.

Authors:  Karl Schilling; John Oberdick
Journal:  Cerebellum       Date:  2009-06-25       Impact factor: 3.847

2.  Expression of mRNAs of multiple growth factors and receptors by astrocytes and glioma cells: detection with reverse transcription-polymerase chain reaction.

Authors:  A Zaheer; W Zhong; E Y Uc; D R Moser; R Lim
Journal:  Cell Mol Neurobiol       Date:  1995-04       Impact factor: 5.046

3.  Expression of mRNAs of multiple growth factors and receptors by neuronal cell lines: detection with RT-PCR.

Authors:  A Zaheer; W Zhong; R Lim
Journal:  Neurochem Res       Date:  1995-12       Impact factor: 3.996

Review 4.  The road less travelled: c-kit and stem cell factor.

Authors:  W Hamel; M Westphal
Journal:  J Neurooncol       Date:  1997-12       Impact factor: 4.130

5.  Cellular mechanisms and behavioral consequences of Kv1.2 regulation in the rat cerebellum.

Authors:  Michael R Williams; Jason R Fuchs; John T Green; Anthony D Morielli
Journal:  J Neurosci       Date:  2012-07-04       Impact factor: 6.167

Review 6.  c-kit(+) cells: the tell-tale heart of cardiac regeneration?

Authors:  Patrizia Nigro; Gianluca Lorenzo Perrucci; Aoife Gowran; Marco Zanobini; Maurizio C Capogrossi; Giulio Pompilio
Journal:  Cell Mol Life Sci       Date:  2015-01-10       Impact factor: 9.261

7.  Stem cell factor stimulates neurogenesis in vitro and in vivo.

Authors:  Kunlin Jin; Xiao Ou Mao; Yunjuan Sun; Lin Xie; David A Greenberg
Journal:  J Clin Invest       Date:  2002-08       Impact factor: 14.808

8.  Administration of anti-c-kit antibody into the cerebrospinal fluid leads to increased cell death in the developing cerebral cortex.

Authors:  Farhad Mashayekhi; Lida Gholizadeh
Journal:  Saudi J Biol Sci       Date:  2011-02-03       Impact factor: 4.219

9.  Gain-of-function mutation of KIT ligand on melanin synthesis causes familial progressive hyperpigmentation.

Authors:  Zhi-Qiang Wang; Lizhen Si; Quan Tang; Debao Lin; Zhangjie Fu; Jing Zhang; Bin Cui; Yufei Zhu; Xianghua Kong; Min Deng; Yu Xia; Heng Xu; Weidong Le; Landian Hu; Xiangyin Kong
Journal:  Am J Hum Genet       Date:  2009-04-16       Impact factor: 11.025

10.  Induced haploinsufficiency of Kit receptor tyrosine kinase impairs brain development.

Authors:  Hitomi Aoki; Akira Hara; Takahiro Kunisada
Journal:  JCI Insight       Date:  2017-10-05
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