The early ontogeny of neuronal nitric oxide synthase systems in the zebrafish.
(2004) In Journal of Experimental Biology 207(Pt 6). p.923-935- Abstract
- To examine a putative role for neuronal nitric oxide synthase (nNOS) in early vertebrate development we investigated nNOS mRNA expression and cGMP production during development of the zebrafish Danio rerio. The nNOS mRNA expression in the central nervous system (CNS) and periphery showed a distinct spatio-temporal pattern in developing zebrafish embryo and young larvae. nNOS mRNA expression was first detected at 19 h postfertilisation (h.p.f.), in a bilateral subpopulation of the embryonic ventrorostral cell cluster in the forebrain. The number of nNOS mRNA-expressing cells in the brain slowly increased, also appearing in the ventrocaudal cell cluster from about 26 h.p.f., and in the dorsorostral and hindbrain cell cluster and in the... (More)
- To examine a putative role for neuronal nitric oxide synthase (nNOS) in early vertebrate development we investigated nNOS mRNA expression and cGMP production during development of the zebrafish Danio rerio. The nNOS mRNA expression in the central nervous system (CNS) and periphery showed a distinct spatio-temporal pattern in developing zebrafish embryo and young larvae. nNOS mRNA expression was first detected at 19 h postfertilisation (h.p.f.), in a bilateral subpopulation of the embryonic ventrorostral cell cluster in the forebrain. The number of nNOS mRNA-expressing cells in the brain slowly increased, also appearing in the ventrocaudal cell cluster from about 26 h.p.f., and in the dorsorostral and hindbrain cell cluster and in the medulla at 30 h.p.f. A major increase in nNOS mRNA expression started at about 40 h.p.f., and by 55 h.p.f. the expression constituted cell populations in differentiated central nuclei and in association with the proliferation zones of the brain, and in the medulla and retina. In parts of the skin, nNOS mRNA expression started at 20 h.p.f. and ended at 55 h.p.f. Between 40 and 55 h.p.f., nNOS mRNA expression started in peripheral organs, forming distinct populations after hatching within or in the vicinity of the presumptive swim bladder, enteric ganglia, and along the alimentary tract and nephritic ducts. Expression of nNOS mRNA correlated with the neuronal differentiation pattern and with the timing and degree of cGMP production. These studies indicate spatio-temporal actions by NO during embryogenesis in the formation of the central and peripheral nervous system, with possible involvement in processes such as neurogenesis, organogenesis and early physiology. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/120674
- author
- Holmqvist, Bo LU ; Ellingsen, B ; Forsell, Johan LU ; Zhdanova, I and Alm, Per LU
- organization
- publishing date
- 2004
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- morphogenesis, Danio rerio, brain, retina, gut, neuronal, regeneration, differentiation, development, in situ, hybridisation, intestine, zebrafish
- in
- Journal of Experimental Biology
- volume
- 207
- issue
- Pt 6
- pages
- 923 - 935
- publisher
- The Company of Biologists Ltd
- external identifiers
-
- pmid:14766951
- wos:000220336500009
- scopus:1642358516
- ISSN
- 1477-9145
- DOI
- 10.1242/jeb.00845
- language
- English
- LU publication?
- yes
- additional info
- The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Pathology, (Lund) (013030000)
- id
- 73414caa-9975-4737-bf42-e085f044f99f (old id 120674)
- alternative location
- http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=14766951&dopt=Abstract
- date added to LUP
- 2016-04-01 11:50:26
- date last changed
- 2022-01-26 19:03:29
@article{73414caa-9975-4737-bf42-e085f044f99f,
abstract = {{To examine a putative role for neuronal nitric oxide synthase (nNOS) in early vertebrate development we investigated nNOS mRNA expression and cGMP production during development of the zebrafish Danio rerio. The nNOS mRNA expression in the central nervous system (CNS) and periphery showed a distinct spatio-temporal pattern in developing zebrafish embryo and young larvae. nNOS mRNA expression was first detected at 19 h postfertilisation (h.p.f.), in a bilateral subpopulation of the embryonic ventrorostral cell cluster in the forebrain. The number of nNOS mRNA-expressing cells in the brain slowly increased, also appearing in the ventrocaudal cell cluster from about 26 h.p.f., and in the dorsorostral and hindbrain cell cluster and in the medulla at 30 h.p.f. A major increase in nNOS mRNA expression started at about 40 h.p.f., and by 55 h.p.f. the expression constituted cell populations in differentiated central nuclei and in association with the proliferation zones of the brain, and in the medulla and retina. In parts of the skin, nNOS mRNA expression started at 20 h.p.f. and ended at 55 h.p.f. Between 40 and 55 h.p.f., nNOS mRNA expression started in peripheral organs, forming distinct populations after hatching within or in the vicinity of the presumptive swim bladder, enteric ganglia, and along the alimentary tract and nephritic ducts. Expression of nNOS mRNA correlated with the neuronal differentiation pattern and with the timing and degree of cGMP production. These studies indicate spatio-temporal actions by NO during embryogenesis in the formation of the central and peripheral nervous system, with possible involvement in processes such as neurogenesis, organogenesis and early physiology.}},
author = {{Holmqvist, Bo and Ellingsen, B and Forsell, Johan and Zhdanova, I and Alm, Per}},
issn = {{1477-9145}},
keywords = {{morphogenesis; Danio rerio; brain; retina; gut; neuronal; regeneration; differentiation; development; in situ; hybridisation; intestine; zebrafish}},
language = {{eng}},
number = {{Pt 6}},
pages = {{923--935}},
publisher = {{The Company of Biologists Ltd}},
series = {{Journal of Experimental Biology}},
title = {{The early ontogeny of neuronal nitric oxide synthase systems in the zebrafish.}},
url = {{http://dx.doi.org/10.1242/jeb.00845}},
doi = {{10.1242/jeb.00845}},
volume = {{207}},
year = {{2004}},
}