Characterization of NGF, trkANGFR, and p75NTR in Retina of Mice Lacking Reelin Glycoprotein

Both Reelin and Nerve Growth Factor (NGF) exert crucial roles in retinal development. Retinogenesis is severely impaired in E-reeler mice, a model of Reelin deficiency showing specific Green Fluorescent Protein expression in Rod Bipolar Cells (RBCs). Since no data are available on Reelin and NGF cro...

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Main Authors: Bijorn Omar Balzamino, Filippo Biamonte, Graziana Esposito, Ramona Marino, Francesca Fanelli, Flavio Keller, Alessandra Micera
Format: Article
Language:English
Published: Wiley 2014-01-01
Series:International Journal of Cell Biology
Online Access:http://dx.doi.org/10.1155/2014/725928
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author Bijorn Omar Balzamino
Filippo Biamonte
Graziana Esposito
Ramona Marino
Francesca Fanelli
Flavio Keller
Alessandra Micera
author_facet Bijorn Omar Balzamino
Filippo Biamonte
Graziana Esposito
Ramona Marino
Francesca Fanelli
Flavio Keller
Alessandra Micera
author_sort Bijorn Omar Balzamino
collection DOAJ
description Both Reelin and Nerve Growth Factor (NGF) exert crucial roles in retinal development. Retinogenesis is severely impaired in E-reeler mice, a model of Reelin deficiency showing specific Green Fluorescent Protein expression in Rod Bipolar Cells (RBCs). Since no data are available on Reelin and NGF cross-talk, NGF and trkANGFR/ p75NTR expression was investigated in retinas from E-reeler versus control mice, by confocal microscopy, Western blotting, and real time PCR analysis. A scattered increase of NGF protein was observed in the Ganglion Cell Layer and more pronounced in the Inner Nuclear Layer (INL). A selective increase of p75NTR was detected in most of RBCs and in other cell subtypes of INL. On the contrary, a slight trend towards a decrease was detected for trkANGFR, albeit not significant. Confocal data were validated by Western blot and real time PCR. Finally, the decreased trkANGFR/ p75NTR ratio, representative of p75NTR increase, significantly correlated with E-reeler versus E-control. These data indicate that NGF-trkANGFR/ p75NTR is affected in E-reeler retina and that p75NTR might represent the main NGF receptor involved in the process. This first NGF-trkANGFR/ p75NTR characterization suggests that E-reeler might be suitable for exploring Reelin-NGF cross-talk, representing an additional information source in those pathologies characterized by retinal degeneration.
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spelling doaj-art-050af7ff89bd41a2a3d59b5615846c602025-02-03T05:51:48ZengWileyInternational Journal of Cell Biology1687-88761687-88842014-01-01201410.1155/2014/725928725928Characterization of NGF, trkANGFR, and p75NTR in Retina of Mice Lacking Reelin GlycoproteinBijorn Omar Balzamino0Filippo Biamonte1Graziana Esposito2Ramona Marino3Francesca Fanelli4Flavio Keller5Alessandra Micera6IRCCS-G.B. Bietti Foundation, Rome, ItalyInstitute of Histology and Embryology, School of Medicine “A. Gemelli”, Catholic University of the Sacred Heart, Rome, ItalyIRCCS-G.B. Bietti Foundation, Rome, ItalyLaboratory of Developmental Neuroscience and Neural Plasticity, University Campus Bio-Medico, Rome, ItalyLaboratory of Developmental Neuroscience and Neural Plasticity, University Campus Bio-Medico, Rome, ItalyLaboratory of Developmental Neuroscience and Neural Plasticity, University Campus Bio-Medico, Rome, ItalyIRCCS-G.B. Bietti Foundation, Rome, ItalyBoth Reelin and Nerve Growth Factor (NGF) exert crucial roles in retinal development. Retinogenesis is severely impaired in E-reeler mice, a model of Reelin deficiency showing specific Green Fluorescent Protein expression in Rod Bipolar Cells (RBCs). Since no data are available on Reelin and NGF cross-talk, NGF and trkANGFR/ p75NTR expression was investigated in retinas from E-reeler versus control mice, by confocal microscopy, Western blotting, and real time PCR analysis. A scattered increase of NGF protein was observed in the Ganglion Cell Layer and more pronounced in the Inner Nuclear Layer (INL). A selective increase of p75NTR was detected in most of RBCs and in other cell subtypes of INL. On the contrary, a slight trend towards a decrease was detected for trkANGFR, albeit not significant. Confocal data were validated by Western blot and real time PCR. Finally, the decreased trkANGFR/ p75NTR ratio, representative of p75NTR increase, significantly correlated with E-reeler versus E-control. These data indicate that NGF-trkANGFR/ p75NTR is affected in E-reeler retina and that p75NTR might represent the main NGF receptor involved in the process. This first NGF-trkANGFR/ p75NTR characterization suggests that E-reeler might be suitable for exploring Reelin-NGF cross-talk, representing an additional information source in those pathologies characterized by retinal degeneration.http://dx.doi.org/10.1155/2014/725928
spellingShingle Bijorn Omar Balzamino
Filippo Biamonte
Graziana Esposito
Ramona Marino
Francesca Fanelli
Flavio Keller
Alessandra Micera
Characterization of NGF, trkANGFR, and p75NTR in Retina of Mice Lacking Reelin Glycoprotein
International Journal of Cell Biology
title Characterization of NGF, trkANGFR, and p75NTR in Retina of Mice Lacking Reelin Glycoprotein
title_full Characterization of NGF, trkANGFR, and p75NTR in Retina of Mice Lacking Reelin Glycoprotein
title_fullStr Characterization of NGF, trkANGFR, and p75NTR in Retina of Mice Lacking Reelin Glycoprotein
title_full_unstemmed Characterization of NGF, trkANGFR, and p75NTR in Retina of Mice Lacking Reelin Glycoprotein
title_short Characterization of NGF, trkANGFR, and p75NTR in Retina of Mice Lacking Reelin Glycoprotein
title_sort characterization of ngf trkangfr and p75ntr in retina of mice lacking reelin glycoprotein
url http://dx.doi.org/10.1155/2014/725928
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