Literature DB >> 2129045

Differential regulation of peripherin and neurofilament gene expression in regenerating rat DRG neurons.

J Wong1, M M Oblinger.   

Abstract

Quantitative in situ hybridization and RNA blotting methods were used to define the time course and magnitude of changes in expression of mRNAs encoding peripherin and the neurofilament (NF) triplet proteins in rat dorsal root ganglion (DRG) neurons during axonal regeneration. mRNA levels in adult rat L4 and L5 DRGs were examined in autoradiograms after in situ hybridization with specific 35S-labeled cDNA probes 1-56 days following unilateral crush lesions of the sciatic nerve. The results of quantitative analyses indicated that peripherin mRNA levels were significantly increased in large-sized (greater than 1000 microns 2) DRG neurons at 7, 14, and 28 days after axotomy while the mRNA levels for each of the NF triplet proteins were significantly decreased at these same time points. The mRNA levels of the low (NF-L) and middle (NF-M) sized NF subunits were significantly decreased as early as 1 day postaxotomy but the mRNA level of the large NF subunit (NF-H) did not change until 7 days after axotomy. The maximal reduction in NF mRNA levels was observed at 14 days postaxotomy when NF-L mRNA levels were only 35% of those in large-sized, normal control neurons. Recovery toward normal levels of both NF and peripherin mRNAs was observed at 8 weeks postaxotomy. RNA blot analyses with total RNA obtained from DRGs at different postaxotomy times confirmed that NF-L mRNA levels were reduced in the DRG during the first 4 weeks after axotomy but, interestingly, failed to detect an increase in peripherin mRNA levels. This difference concerning peripherin mRNA levels in axotomized preparations obtained by RNA blotting vs. in situ hybridization was attributed to the fact that RNA blots utilized total DRG RNA which includes mRNAs from both small and large-sized DRG neurons. A recent in situ hybridization study showed that the small-sized DRG neurons which contain the majority of the peripherin mRNA in the DRG do not increase their peripherin mRNA levels 14 days after axotomy (Oblinger et al., 1989b). This may mask any change in the large neuron response when total RNA is examined. Overall, the results of this study demonstrate (1) that type III (peripherin) and type IV (NF) intermediate filament genes are regulated differently during axonal regeneration, and (2) that the three NF genes are down-regulated in a fairly coordinate manner during regeneration. These data suggest that an important component of the regeneration program is the alteration of the composition of the IF component of the cytoskeleton.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1990        PMID: 2129045     DOI: 10.1002/jnr.490270312

Source DB:  PubMed          Journal:  J Neurosci Res        ISSN: 0360-4012            Impact factor:   4.164


  15 in total

1.  Peripherin is a subunit of peripheral nerve neurofilaments: implications for differential vulnerability of CNS and peripheral nervous system axons.

Authors:  Aidong Yuan; Takahiro Sasaki; Asok Kumar; Corrinne M Peterhoff; Mala V Rao; Ronald K Liem; Jean-Pierre Julien; Ralph A Nixon
Journal:  J Neurosci       Date:  2012-06-20       Impact factor: 6.167

2.  Recovery of neurofilament expression selectively in regenerating reticulospinal neurons.

Authors:  A J Jacobs; G P Swain; J A Snedeker; D S Pijak; L J Gladstone; M E Selzer
Journal:  J Neurosci       Date:  1997-07-01       Impact factor: 6.167

Review 3.  Microtubule-associated proteins (MAPs) in the peripheral nervous system during development and regeneration.

Authors:  J Nunez; I Fischer
Journal:  J Mol Neurosci       Date:  1997-06       Impact factor: 3.444

4.  Small proline-rich repeat protein 1A is expressed by axotomized neurons and promotes axonal outgrowth.

Authors:  Iris E Bonilla; Katsuhisa Tanabe; Stephen M Strittmatter
Journal:  J Neurosci       Date:  2002-02-15       Impact factor: 6.167

5.  Optically Guided Single Cell Mass Spectrometry of Rat Dorsal Root Ganglia to Profile Lipids, Peptides and Proteins.

Authors:  Thanh D Do; Joseph F Ellis; Elizabeth K Neumann; Troy J Comi; Emily G Tillmaand; Ashley E Lenhart; Stanislav S Rubakhin; Jonathan V Sweedler
Journal:  Chemphyschem       Date:  2018-04-17       Impact factor: 3.102

6.  Transgenic mice expressing the Peripherin-EGFP genomic reporter display intrinsic peripheral nervous system fluorescence.

Authors:  Samuel McLenachan; Yona Goldshmit; Kerry J Fowler; Lucille Voullaire; Timothy P Holloway; Ann M Turnley; Panos A Ioannou; Joseph P Sarsero
Journal:  Transgenic Res       Date:  2008-08-15       Impact factor: 2.788

Review 7.  Type III Intermediate Filaments Desmin, Glial Fibrillary Acidic Protein (GFAP), Vimentin, and Peripherin.

Authors:  Elly M Hol; Yassemi Capetanaki
Journal:  Cold Spring Harb Perspect Biol       Date:  2017-12-01       Impact factor: 10.005

8.  Cell-specific transcription of the peripherin gene in neuronal cell lines involves a cis-acting element surrounding the TATA box.

Authors:  D Desmarais; M Filion; L Lapointe; A Royal
Journal:  EMBO J       Date:  1992-08       Impact factor: 11.598

9.  gp130 cytokines are positive signals triggering changes in gene expression and axon outgrowth in peripheral neurons following injury.

Authors:  Richard E Zigmond
Journal:  Front Mol Neurosci       Date:  2012-01-20       Impact factor: 5.639

10.  Charcot-Marie-Tooth type 2B disease-causing RAB7A mutant proteins show altered interaction with the neuronal intermediate filament peripherin.

Authors:  Laura Cogli; Cinzia Progida; Claire L Thomas; Bradley Spencer-Dene; Claudia Donno; Giampietro Schiavo; Cecilia Bucci
Journal:  Acta Neuropathol       Date:  2012-11-23       Impact factor: 17.088

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