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Comparative lipid profiling dataset of the inflammation-induced optic nerve regeneration

In adult mammals, retinal ganglion cells (RGCs) fail to regenerate following damage. As a result, RGCs die after acute injury and in progressive degenerative diseases such as glaucoma; this can lead to permanent vision loss and, eventually, blindness. Lipids are crucial for the development and maint...

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Autores principales: Trzeciecka, Anna, Stark, David T., Kwong, Jacky M.K., Piqueras, Maria, Bhattacharya, Sanjoy K., Caprioli, Joseph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6517575/
https://www.ncbi.nlm.nih.gov/pubmed/31193141
http://dx.doi.org/10.1016/j.dib.2019.103950
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author Trzeciecka, Anna
Stark, David T.
Kwong, Jacky M.K.
Piqueras, Maria
Bhattacharya, Sanjoy K.
Caprioli, Joseph
author_facet Trzeciecka, Anna
Stark, David T.
Kwong, Jacky M.K.
Piqueras, Maria
Bhattacharya, Sanjoy K.
Caprioli, Joseph
author_sort Trzeciecka, Anna
collection PubMed
description In adult mammals, retinal ganglion cells (RGCs) fail to regenerate following damage. As a result, RGCs die after acute injury and in progressive degenerative diseases such as glaucoma; this can lead to permanent vision loss and, eventually, blindness. Lipids are crucial for the development and maintenance of cell membranes, myelin sheaths, and cellular signaling pathways, however, little is known about their role in axon injury and repair. Studies examining changes to the lipidome during optic nerve (ON) regeneration could greatly inform treatment strategies, yet these are largely lacking. Experimental animal models of ON regeneration have facilitated the exploration of the molecular determinants that affect RGC axon regeneration. Here, we analyzed lipid profiles of the ON and retina in an ON crush rat model using liquid chromatography–mass spectrometry. Furthermore, we investigated lipidome changes after ON crush followed by intravitreal treatment with Zymosan, a yeast cell wall derivative known to enhance RGC regeneration. This data is available at the NIH Common Fund's Metabolomics Data Repository and Coordinating Center (supported by NIH grant, U01-DK097430) website, the Metabolomics Workbench, http://www.metabolomicsworkbench.org, where it has been assigned Project ID: PR000661. The data can be accessed directly via it's Project DOI: doi: 10.21,228/M87D53.
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spelling pubmed-65175752019-05-21 Comparative lipid profiling dataset of the inflammation-induced optic nerve regeneration Trzeciecka, Anna Stark, David T. Kwong, Jacky M.K. Piqueras, Maria Bhattacharya, Sanjoy K. Caprioli, Joseph Data Brief Biochemistry, Genetics and Molecular Biology In adult mammals, retinal ganglion cells (RGCs) fail to regenerate following damage. As a result, RGCs die after acute injury and in progressive degenerative diseases such as glaucoma; this can lead to permanent vision loss and, eventually, blindness. Lipids are crucial for the development and maintenance of cell membranes, myelin sheaths, and cellular signaling pathways, however, little is known about their role in axon injury and repair. Studies examining changes to the lipidome during optic nerve (ON) regeneration could greatly inform treatment strategies, yet these are largely lacking. Experimental animal models of ON regeneration have facilitated the exploration of the molecular determinants that affect RGC axon regeneration. Here, we analyzed lipid profiles of the ON and retina in an ON crush rat model using liquid chromatography–mass spectrometry. Furthermore, we investigated lipidome changes after ON crush followed by intravitreal treatment with Zymosan, a yeast cell wall derivative known to enhance RGC regeneration. This data is available at the NIH Common Fund's Metabolomics Data Repository and Coordinating Center (supported by NIH grant, U01-DK097430) website, the Metabolomics Workbench, http://www.metabolomicsworkbench.org, where it has been assigned Project ID: PR000661. The data can be accessed directly via it's Project DOI: doi: 10.21,228/M87D53. Elsevier 2019-04-25 /pmc/articles/PMC6517575/ /pubmed/31193141 http://dx.doi.org/10.1016/j.dib.2019.103950 Text en © 2019 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Biochemistry, Genetics and Molecular Biology
Trzeciecka, Anna
Stark, David T.
Kwong, Jacky M.K.
Piqueras, Maria
Bhattacharya, Sanjoy K.
Caprioli, Joseph
Comparative lipid profiling dataset of the inflammation-induced optic nerve regeneration
title Comparative lipid profiling dataset of the inflammation-induced optic nerve regeneration
title_full Comparative lipid profiling dataset of the inflammation-induced optic nerve regeneration
title_fullStr Comparative lipid profiling dataset of the inflammation-induced optic nerve regeneration
title_full_unstemmed Comparative lipid profiling dataset of the inflammation-induced optic nerve regeneration
title_short Comparative lipid profiling dataset of the inflammation-induced optic nerve regeneration
title_sort comparative lipid profiling dataset of the inflammation-induced optic nerve regeneration
topic Biochemistry, Genetics and Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6517575/
https://www.ncbi.nlm.nih.gov/pubmed/31193141
http://dx.doi.org/10.1016/j.dib.2019.103950
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