Design of an Approach to Characterize CD11b Cre x LoxP BDNF Deletion in Mice: Implications for Neuropathic Pain

Background: An approach designed to characterize BDNF gene deletion within microglia of the dorsal horn of the spinal cord does not currently exist. Therefore, my goal was to develop methods to assess Cre- mediated BDNF deletion. To this end I designed and tested two different approaches focusing on...

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Main Author: Marciniak, Robert
Other Authors: Salter, Michael
Language:en_ca
Published: 2012
Subjects:
Online Access:http://hdl.handle.net/1807/33440
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spelling ndltd-LACETR-oai-collectionscanada.gc.ca-OTU.1807-334402013-04-20T05:22:25ZDesign of an Approach to Characterize CD11b Cre x LoxP BDNF Deletion in Mice: Implications for Neuropathic PainMarciniak, RobertBDNFNeuropathic Pain0317Background: An approach designed to characterize BDNF gene deletion within microglia of the dorsal horn of the spinal cord does not currently exist. Therefore, my goal was to develop methods to assess Cre- mediated BDNF deletion. To this end I designed and tested two different approaches focusing on the aspects of BDNF mRNA expression or genomic level gene deletion. Methods: Approach 1: BDNF messenger RNA was detected by in situ hybridization. Approach 2: BDNF gene deletion was detected by a positive signal semi-quantitative Polymerase Chain Reaction (PCR). Results: In situ hybridization detected spinal BDNF and regional changes in BDNF mRNA following PNI in wild-type mice. The BDNF PCR detected Cre-mediated BDNF deletions in transgenic animals. Conclusion: Two approaches have been developed and initial tests of these approaches show promising results and will provide valuable tools for researchers investigating BDNF deletion in transgenic animals.Salter, Michael2012-112012-11-22T17:05:32ZNO_RESTRICTION2012-11-22T17:05:32Z2012-11-22Thesishttp://hdl.handle.net/1807/33440en_ca
collection NDLTD
language en_ca
sources NDLTD
topic BDNF
Neuropathic Pain
0317
spellingShingle BDNF
Neuropathic Pain
0317
Marciniak, Robert
Design of an Approach to Characterize CD11b Cre x LoxP BDNF Deletion in Mice: Implications for Neuropathic Pain
description Background: An approach designed to characterize BDNF gene deletion within microglia of the dorsal horn of the spinal cord does not currently exist. Therefore, my goal was to develop methods to assess Cre- mediated BDNF deletion. To this end I designed and tested two different approaches focusing on the aspects of BDNF mRNA expression or genomic level gene deletion. Methods: Approach 1: BDNF messenger RNA was detected by in situ hybridization. Approach 2: BDNF gene deletion was detected by a positive signal semi-quantitative Polymerase Chain Reaction (PCR). Results: In situ hybridization detected spinal BDNF and regional changes in BDNF mRNA following PNI in wild-type mice. The BDNF PCR detected Cre-mediated BDNF deletions in transgenic animals. Conclusion: Two approaches have been developed and initial tests of these approaches show promising results and will provide valuable tools for researchers investigating BDNF deletion in transgenic animals.
author2 Salter, Michael
author_facet Salter, Michael
Marciniak, Robert
author Marciniak, Robert
author_sort Marciniak, Robert
title Design of an Approach to Characterize CD11b Cre x LoxP BDNF Deletion in Mice: Implications for Neuropathic Pain
title_short Design of an Approach to Characterize CD11b Cre x LoxP BDNF Deletion in Mice: Implications for Neuropathic Pain
title_full Design of an Approach to Characterize CD11b Cre x LoxP BDNF Deletion in Mice: Implications for Neuropathic Pain
title_fullStr Design of an Approach to Characterize CD11b Cre x LoxP BDNF Deletion in Mice: Implications for Neuropathic Pain
title_full_unstemmed Design of an Approach to Characterize CD11b Cre x LoxP BDNF Deletion in Mice: Implications for Neuropathic Pain
title_sort design of an approach to characterize cd11b cre x loxp bdnf deletion in mice: implications for neuropathic pain
publishDate 2012
url http://hdl.handle.net/1807/33440
work_keys_str_mv AT marciniakrobert designofanapproachtocharacterizecd11bcrexloxpbdnfdeletioninmiceimplicationsforneuropathicpain
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