Morphological changes in different populations of bladder afferent neurons detected by herpes simplex virus (HSV) vectors with cell-type-specific promoters in mice with spinal cord injury. (19th November 2017)
- Record Type:
- Journal Article
- Title:
- Morphological changes in different populations of bladder afferent neurons detected by herpes simplex virus (HSV) vectors with cell-type-specific promoters in mice with spinal cord injury. (19th November 2017)
- Main Title:
- Morphological changes in different populations of bladder afferent neurons detected by herpes simplex virus (HSV) vectors with cell-type-specific promoters in mice with spinal cord injury
- Authors:
- Shimizu, Nobutaka
Doyal, Mark F.
Goins, William F.
Kadekawa, Katsumi
Wada, Naoki
Kanai, Anthony J.
de Groat, William C.
Hirayama, Akihide
Uemura, Hirotsugu
Glorioso, Joseph C.
Yoshimura, Naoki - Abstract:
- Highlights: A new HSV vector method is useful to identify bladder afferent subpopulations. CGRP-expressing bladder afferent neurons increase their size and number after SCI. TRPV1-expressing neurons increase the number, but decrease the size after SCI. A-fiber bladder neurons may switch their phenotype to express CGRP after SCI. SCI-induced changes in A-fiber afferents may be different between mice and rats. Abstract: Functional and morphological changes in C-fiber bladder afferent pathways are reportedly involved in neurogenic detrusor overactivity (NDO) after spinal cord injury (SCI). This study examined the morphological changes in different populations of bladder afferent neurons after SCI using replication-defective herpes simplex virus (HSV) vectors encoding the mCherry reporter driven by neuronal cell-type-specific promoters. Spinal intact (SI) and SCI mice were injected into the bladder wall with HSV mCherry vectors driven by the cytomegalovirus (CMV) promoter, CGRP promoter, TRPV1 promoter or neurofilament 200 (NF200) promoter. Two weeks after vector inoculation into the bladder wall, L1 and L6 dorsal root ganglia (DRG) were removed bilaterally for immunofluorescent staining using anti-mCherry antibody. The number of CMV promoter vector-labeled neurons was not altered after SCI. The number of CGRP and TRPV1 promoter vector-labeled neurons was significantly increased whereas the number of NF200 vector-labeled neurons was decreased in L6 DRG after SCI. The median sizeHighlights: A new HSV vector method is useful to identify bladder afferent subpopulations. CGRP-expressing bladder afferent neurons increase their size and number after SCI. TRPV1-expressing neurons increase the number, but decrease the size after SCI. A-fiber bladder neurons may switch their phenotype to express CGRP after SCI. SCI-induced changes in A-fiber afferents may be different between mice and rats. Abstract: Functional and morphological changes in C-fiber bladder afferent pathways are reportedly involved in neurogenic detrusor overactivity (NDO) after spinal cord injury (SCI). This study examined the morphological changes in different populations of bladder afferent neurons after SCI using replication-defective herpes simplex virus (HSV) vectors encoding the mCherry reporter driven by neuronal cell-type-specific promoters. Spinal intact (SI) and SCI mice were injected into the bladder wall with HSV mCherry vectors driven by the cytomegalovirus (CMV) promoter, CGRP promoter, TRPV1 promoter or neurofilament 200 (NF200) promoter. Two weeks after vector inoculation into the bladder wall, L1 and L6 dorsal root ganglia (DRG) were removed bilaterally for immunofluorescent staining using anti-mCherry antibody. The number of CMV promoter vector-labeled neurons was not altered after SCI. The number of CGRP and TRPV1 promoter vector-labeled neurons was significantly increased whereas the number of NF200 vector-labeled neurons was decreased in L6 DRG after SCI. The median size of CGRP promoter-labeled C-fiber neurons was increased from 247.0 in SI mice to 271.3 μm 2 in SCI mice whereas the median cell size of TRPV1 promoter vector-labeled neurons was decreased from 245.2 in SI mice to 216.5 μm 2 in SCI mice. CGRP and TRPV1 mRNA levels of laser-captured bladder afferent neurons labeled with Fast Blue were significantly increased in SCI mice compared to SI mice. Thus, using a novel HSV vector-mediated neuronal labeling technique, we found that SCI induces expansion of the CGRP- and TRPV1-expressing C-fiber cell population, which could contribute to C-fiber afferent hyperexcitability and NDO after SCI. … (more)
- Is Part Of:
- Neuroscience. Volume 364(2017)
- Journal:
- Neuroscience
- Issue:
- Volume 364(2017)
- Issue Display:
- Volume 364, Issue 2017 (2017)
- Year:
- 2017
- Volume:
- 364
- Issue:
- 2017
- Issue Sort Value:
- 2017-0364-2017-0000
- Page Start:
- 190
- Page End:
- 201
- Publication Date:
- 2017-11-19
- Subjects:
- CGRP calcitonin gene-related peptide -- CMV cytomegalovirus -- CPE cytopathic effect -- DRG dorsal root ganglia -- EUS external urethral sphincter -- FB Fast Blue -- GAD glutamic acid decarboxylase -- HSV herpes simplex virus -- i.p. intraperitoneal -- IVP intravesical pressure -- LAT latency associated transcript -- LCM laser capture microdissection -- LUTD lower urinary tract dysfunction -- MOI multiplicity of infection -- NDO neurogenic detrusor overactivity -- NF neurofilament -- NF200 neurofilament 200 -- PBS phosphate-buffered saline -- RTx resiniferatoxin -- SCI spinal cord injury -- SI spinal intact
herpes simplex virus vector -- spinal cord injury -- mouse -- urinary bladder -- dorsal root ganglia -- laser-capture microdissection
Neurochemistry -- Periodicals
Neurophysiology -- Periodicals
Neurology -- Periodicals
Neurochimie -- Périodiques
Neurophysiologie -- Périodiques
Neurochemistry
Neurophysiology
Electronic journals
Periodicals
Electronic journals
612.8 - Journal URLs:
- http://www.sciencedirect.com/science/journal/03064522 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/03064522 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/03064522 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.neuroscience.2017.09.024 ↗
- Languages:
- English
- ISSNs:
- 0306-4522
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- Legaldeposit
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