Lipidomics dataset of PTEN deletion-induced optic nerve regeneration mouse model
The optic nerve is part of the mammalian adult central nervous system (CNS) and has limited capability to regenerate after injury. Deletion of phosphatase and tensin homolog (PTEN), a negative regulator of the PI3 kinase/Akt pathway, has been shown to promote regeneration in retinal ganglion cells (...
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2021-02-01
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doaj-8cb6a3406bcf42308c1865d53d4b6e4c2021-01-02T05:12:56ZengElsevierData in Brief2352-34092021-02-0134106699Lipidomics dataset of PTEN deletion-induced optic nerve regeneration mouse modelJennifer Arcuri0Shane Hegarty1Zhigang He2Sanjoy K. Bhattacharya3Bascom Palmer Eye Institute, Miller School of Medicine at University of Miami, Miami, FL, 33136, USA; Miami Integrative Metabolomics Research Center, Miami, FL, 33136, USA; Molecular Cellular Pharmacology Graduate Program, University of Miami, Miami, FL, 33136, USAF.M. Kirby Neurobiology Center, Department of Neurology, Boston Children's Hospital, Harvard Medical School, 300 Longwood Avenue, Boston, MA 02115, USAF.M. Kirby Neurobiology Center, Department of Neurology, Boston Children's Hospital, Harvard Medical School, 300 Longwood Avenue, Boston, MA 02115, USABascom Palmer Eye Institute, Miller School of Medicine at University of Miami, Miami, FL, 33136, USA; Miami Integrative Metabolomics Research Center, Miami, FL, 33136, USA; Molecular Cellular Pharmacology Graduate Program, University of Miami, Miami, FL, 33136, USA; Corresponding author.The optic nerve is part of the mammalian adult central nervous system (CNS) and has limited capability to regenerate after injury. Deletion of phosphatase and tensin homolog (PTEN), a negative regulator of the PI3 kinase/Akt pathway, has been shown to promote regeneration in retinal ganglion cells (RGCs) after optic nerve injury [1]. We present the lipidome of adult PTENloxP/loxP mice subjected to intravitreal injection of adeno-associated viruses expressing Cre (AAV-Cre) as a model of CNS neuroregeneration. At 4 weeks old, PTENloxP/loxP mice were intravitreally-injected with 2–3 μl of either AAV-Cre (KO) or AAV-PLAP (control), and two weeks later optic nerve crush was performed. At indicated time-points after crush (0 days, 7 days, 14 days), mice were euthanized and optic nerves were immediately dissected out, and then flash frozen on dry ice. A modified Bligh and Dyer [2] method was used for lipid extraction from the optic nerves, followed by liquid chromatography-mass spectrometry (LC MS-MS) lipid profiling using a Q-Exactive Orbitrap instrument coupled with Accela 600 HPLC. The raw scans were analysed with LipidSearch 4.2 and the statistical analysis was conducted through Metaboanalyst 4.0. This data is available at Metabolomics Workbench, study ID ST001477.http://www.sciencedirect.com/science/article/pii/S235234092031578XRegenerationCNS InjuryOptic NervePTENLipids |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jennifer Arcuri Shane Hegarty Zhigang He Sanjoy K. Bhattacharya |
spellingShingle |
Jennifer Arcuri Shane Hegarty Zhigang He Sanjoy K. Bhattacharya Lipidomics dataset of PTEN deletion-induced optic nerve regeneration mouse model Data in Brief Regeneration CNS Injury Optic Nerve PTEN Lipids |
author_facet |
Jennifer Arcuri Shane Hegarty Zhigang He Sanjoy K. Bhattacharya |
author_sort |
Jennifer Arcuri |
title |
Lipidomics dataset of PTEN deletion-induced optic nerve regeneration mouse model |
title_short |
Lipidomics dataset of PTEN deletion-induced optic nerve regeneration mouse model |
title_full |
Lipidomics dataset of PTEN deletion-induced optic nerve regeneration mouse model |
title_fullStr |
Lipidomics dataset of PTEN deletion-induced optic nerve regeneration mouse model |
title_full_unstemmed |
Lipidomics dataset of PTEN deletion-induced optic nerve regeneration mouse model |
title_sort |
lipidomics dataset of pten deletion-induced optic nerve regeneration mouse model |
publisher |
Elsevier |
series |
Data in Brief |
issn |
2352-3409 |
publishDate |
2021-02-01 |
description |
The optic nerve is part of the mammalian adult central nervous system (CNS) and has limited capability to regenerate after injury. Deletion of phosphatase and tensin homolog (PTEN), a negative regulator of the PI3 kinase/Akt pathway, has been shown to promote regeneration in retinal ganglion cells (RGCs) after optic nerve injury [1]. We present the lipidome of adult PTENloxP/loxP mice subjected to intravitreal injection of adeno-associated viruses expressing Cre (AAV-Cre) as a model of CNS neuroregeneration. At 4 weeks old, PTENloxP/loxP mice were intravitreally-injected with 2–3 μl of either AAV-Cre (KO) or AAV-PLAP (control), and two weeks later optic nerve crush was performed. At indicated time-points after crush (0 days, 7 days, 14 days), mice were euthanized and optic nerves were immediately dissected out, and then flash frozen on dry ice. A modified Bligh and Dyer [2] method was used for lipid extraction from the optic nerves, followed by liquid chromatography-mass spectrometry (LC MS-MS) lipid profiling using a Q-Exactive Orbitrap instrument coupled with Accela 600 HPLC. The raw scans were analysed with LipidSearch 4.2 and the statistical analysis was conducted through Metaboanalyst 4.0. This data is available at Metabolomics Workbench, study ID ST001477. |
topic |
Regeneration CNS Injury Optic Nerve PTEN Lipids |
url |
http://www.sciencedirect.com/science/article/pii/S235234092031578X |
work_keys_str_mv |
AT jenniferarcuri lipidomicsdatasetofptendeletioninducedopticnerveregenerationmousemodel AT shanehegarty lipidomicsdatasetofptendeletioninducedopticnerveregenerationmousemodel AT zhiganghe lipidomicsdatasetofptendeletioninducedopticnerveregenerationmousemodel AT sanjoykbhattacharya lipidomicsdatasetofptendeletioninducedopticnerveregenerationmousemodel |
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1724359125479981056 |