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Visualisation of Kiss1 Neurone Distribution Using a Kiss1‐CRE Transgenic Mouse

Kisspeptin neuropeptides are encoded by the Kiss1 gene and play a critical role in the regulation of the mammalian reproductive axis. Kiss1 neurones are found in two locations in the rodent hypothalamus: one in the arcuate nucleus (ARC) and another in the RP3V region, which includes the anteroventra...

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Autores principales: Yeo, S.‐H., Kyle, V., Morris, P. G., Jackman, S., Sinnett‐Smith, L. C., Schacker, M., Chen, C., Colledge, W. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5091624/
https://www.ncbi.nlm.nih.gov/pubmed/27663274
http://dx.doi.org/10.1111/jne.12435
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author Yeo, S.‐H.
Kyle, V.
Morris, P. G.
Jackman, S.
Sinnett‐Smith, L. C.
Schacker, M.
Chen, C.
Colledge, W. H.
author_facet Yeo, S.‐H.
Kyle, V.
Morris, P. G.
Jackman, S.
Sinnett‐Smith, L. C.
Schacker, M.
Chen, C.
Colledge, W. H.
author_sort Yeo, S.‐H.
collection PubMed
description Kisspeptin neuropeptides are encoded by the Kiss1 gene and play a critical role in the regulation of the mammalian reproductive axis. Kiss1 neurones are found in two locations in the rodent hypothalamus: one in the arcuate nucleus (ARC) and another in the RP3V region, which includes the anteroventral periventricular nucleus (AVPV). Detailed mapping of the fibre distribution of Kiss1 neurones will help with our understanding of the action of these neurones in other regions of the brain. We have generated a transgenic mouse in which the Kiss1 coding region is disrupted by a CRE‐GFP transgene so that expression of the CRE recombinase protein is driven from the Kiss1 promoter. As expected, mutant mice of both sexes are sterile with hypogonadotrophic hypogonadism and do not show the normal rise in luteinising hormone after gonadectomy. Mutant female mice do not develop mature Graafian follicles or form corpora lutea consistent with ovulatory failure. Mutant male mice have low blood testosterone levels and impaired spermatogenesis beyond the meiosis stage. Breeding Kiss‐CRE heterozygous mice with CRE‐activated tdTomato reporter mice allows fluorescence visualisation of Kiss1 neurones in brain slices. Approximately 80‐90% of tdTomato positive neurones in the ARC were co‐labelled with kisspeptin and expression of tdTomato in the AVPV region was sexually dimorphic, with higher expression in females than males. A small number of tdTomato‐labelled neurones was also found in other locations, including the lateral septum, the anterodorsal preoptic nucleus, the amygdala, the dorsomedial and ventromedial hypothalamic nuclei, the periaquaductal grey, and the mammillary nucleus. Three dimensional visualisation of Kiss1 neurones and fibres by CLARITY processing of whole brains showed an increase in ARC expression during puberty and higher numbers of Kiss1 neurones in the caudal region of the ARC compared to the rostral region. ARC Kiss1 neurones sent fibre projections to several hypothalamic regions, including rostrally to the periventricular and pre‐optic areas and to the lateral hypothalamus.
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spelling pubmed-50916242016-11-09 Visualisation of Kiss1 Neurone Distribution Using a Kiss1‐CRE Transgenic Mouse Yeo, S.‐H. Kyle, V. Morris, P. G. Jackman, S. Sinnett‐Smith, L. C. Schacker, M. Chen, C. Colledge, W. H. J Neuroendocrinol Original Articles Kisspeptin neuropeptides are encoded by the Kiss1 gene and play a critical role in the regulation of the mammalian reproductive axis. Kiss1 neurones are found in two locations in the rodent hypothalamus: one in the arcuate nucleus (ARC) and another in the RP3V region, which includes the anteroventral periventricular nucleus (AVPV). Detailed mapping of the fibre distribution of Kiss1 neurones will help with our understanding of the action of these neurones in other regions of the brain. We have generated a transgenic mouse in which the Kiss1 coding region is disrupted by a CRE‐GFP transgene so that expression of the CRE recombinase protein is driven from the Kiss1 promoter. As expected, mutant mice of both sexes are sterile with hypogonadotrophic hypogonadism and do not show the normal rise in luteinising hormone after gonadectomy. Mutant female mice do not develop mature Graafian follicles or form corpora lutea consistent with ovulatory failure. Mutant male mice have low blood testosterone levels and impaired spermatogenesis beyond the meiosis stage. Breeding Kiss‐CRE heterozygous mice with CRE‐activated tdTomato reporter mice allows fluorescence visualisation of Kiss1 neurones in brain slices. Approximately 80‐90% of tdTomato positive neurones in the ARC were co‐labelled with kisspeptin and expression of tdTomato in the AVPV region was sexually dimorphic, with higher expression in females than males. A small number of tdTomato‐labelled neurones was also found in other locations, including the lateral septum, the anterodorsal preoptic nucleus, the amygdala, the dorsomedial and ventromedial hypothalamic nuclei, the periaquaductal grey, and the mammillary nucleus. Three dimensional visualisation of Kiss1 neurones and fibres by CLARITY processing of whole brains showed an increase in ARC expression during puberty and higher numbers of Kiss1 neurones in the caudal region of the ARC compared to the rostral region. ARC Kiss1 neurones sent fibre projections to several hypothalamic regions, including rostrally to the periventricular and pre‐optic areas and to the lateral hypothalamus. John Wiley and Sons Inc. 2016-10-28 2016-11 /pmc/articles/PMC5091624/ /pubmed/27663274 http://dx.doi.org/10.1111/jne.12435 Text en © 2016 The Authors. Journal of Neuroendocrinology published by John Wiley & Sons Ltd on behalf of British Society for Neuroendocrinology. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Yeo, S.‐H.
Kyle, V.
Morris, P. G.
Jackman, S.
Sinnett‐Smith, L. C.
Schacker, M.
Chen, C.
Colledge, W. H.
Visualisation of Kiss1 Neurone Distribution Using a Kiss1‐CRE Transgenic Mouse
title Visualisation of Kiss1 Neurone Distribution Using a Kiss1‐CRE Transgenic Mouse
title_full Visualisation of Kiss1 Neurone Distribution Using a Kiss1‐CRE Transgenic Mouse
title_fullStr Visualisation of Kiss1 Neurone Distribution Using a Kiss1‐CRE Transgenic Mouse
title_full_unstemmed Visualisation of Kiss1 Neurone Distribution Using a Kiss1‐CRE Transgenic Mouse
title_short Visualisation of Kiss1 Neurone Distribution Using a Kiss1‐CRE Transgenic Mouse
title_sort visualisation of kiss1 neurone distribution using a kiss1‐cre transgenic mouse
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5091624/
https://www.ncbi.nlm.nih.gov/pubmed/27663274
http://dx.doi.org/10.1111/jne.12435
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