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Hypothalamic projections to the optic tectum in larval zebrafish

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Hypothalamic projections to the optic tectum in larval zebrafish. / Heap, Lucy A.; Vanwalleghem, Gilles C.; Thompson, Andrew W. et al.

In: Frontiers in Neuroanatomy, Vol. 11, 135, 17.01.2018.

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

Harvard

Heap, LA, Vanwalleghem, GC, Thompson, AW, Favre-Bulle, I, Rubinsztein-Dunlop, H & Scott, EK 2018, 'Hypothalamic projections to the optic tectum in larval zebrafish', Frontiers in Neuroanatomy, vol. 11, 135. https://doi.org/10.3389/fnana.2017.00135

APA

Heap, L. A., Vanwalleghem, G. C., Thompson, A. W., Favre-Bulle, I., Rubinsztein-Dunlop, H., & Scott, E. K. (2018). Hypothalamic projections to the optic tectum in larval zebrafish. Frontiers in Neuroanatomy, 11, [135]. https://doi.org/10.3389/fnana.2017.00135

CBE

Heap LA, Vanwalleghem GC, Thompson AW, Favre-Bulle I, Rubinsztein-Dunlop H, Scott EK. 2018. Hypothalamic projections to the optic tectum in larval zebrafish. Frontiers in Neuroanatomy. 11:Article 135. https://doi.org/10.3389/fnana.2017.00135

MLA

Vancouver

Heap LA, Vanwalleghem GC, Thompson AW, Favre-Bulle I, Rubinsztein-Dunlop H, Scott EK. Hypothalamic projections to the optic tectum in larval zebrafish. Frontiers in Neuroanatomy. 2018 Jan 17;11:135. doi: 10.3389/fnana.2017.00135

Author

Heap, Lucy A. ; Vanwalleghem, Gilles C. ; Thompson, Andrew W. et al. / Hypothalamic projections to the optic tectum in larval zebrafish. In: Frontiers in Neuroanatomy. 2018 ; Vol. 11.

Bibtex

@article{b4b21be2c5534347ba3c3d71f65e883f,
title = "Hypothalamic projections to the optic tectum in larval zebrafish",
abstract = "The optic tectum of larval zebrafish is an important model for understanding visual processing in vertebrates. The tectum has been traditionally viewed as dominantly visual, with a majority of studies focusing on the processes by which tectal circuits receive and process retinally-derived visual information. Recently, a handful of studies have shown a much more complex role for the optic tectum in larval zebrafish, and anatomical and functional data from these studies suggest that this role extends beyond the visual system, and beyond the processing of exclusively retinal inputs. Consistent with this evolving view of the tectum, we have used a Gal4 enhancer trap line to identify direct projections from rostral hypothalamus (RH) to the tectal neuropil of larval zebrafish. These projections ramify within the deepest laminae of the tectal neuropil, the stratum album centrale (SAC)/stratum griseum periventriculare (SPV), and also innervate strata distinct from those innervated by retinal projections. Using optogenetic stimulation of the hypothalamic projection neurons paired with calcium imaging in the tectum, we find rebound firing in tectal neurons consistent with hypothalamic inhibitory input. Our results suggest that tectal processing in larval zebrafish is modulated by hypothalamic inhibitory inputs to the deep tectal neuropil.",
keywords = "Hypothalamus, Optogenetics, SPIM (selective plane illumination microscopy), Superior colliculus, Tectum, Zebrafish",
author = "Heap, {Lucy A.} and Vanwalleghem, {Gilles C.} and Thompson, {Andrew W.} and Itia Favre-Bulle and Halina Rubinsztein-Dunlop and Scott, {Ethan K.}",
note = "Funding Information: We thank Rebecca Dunning for creating the PME-linker-MCS plasmid. We are grateful to Karl Deisseroth for providing the Channelrhodopsin-2(ET/TC) plasmid and Misha Ahrens for providing the HuC:H2B-GCaMP6s transgenic line. We thank Owen Randlett, Alexander Schier, and Florian Engert for providing the Z-Brain atlas prior to publication, as well as for assisting in Z-Brain analysis. We thank Jan Kaslin and members of the Scott laboratory for comments on the manuscript. Support was provided by the Australian Research Council Postgraduate Awards to LAH and AWT; an National Health and Medical Research Council (NHMRC) Project Grant (APP1066887), ARC Future Fellowship (FT110100887), a Simons Foundation Explorer Award (336331) and two ARC Discovery Project Grants (DP140102036 and DP110103612) to EKS; an ARC Discovery Project (DP140100753) to HR-D; a UQ Postgraduate Scholarship to IF-B; and an European Molecular Biology Organization (EMBO) Long-term Fellowship (ALTF 727-2014) to GCV. Imaging was performed at the Queensland Brain Institute{\textquoteright}s Advanced Microscopy Facility, generously supported by the Australian Government through the ARC LIEF grant LE130100078. Publisher Copyright: {\textcopyright} 2018 Heap, Vanwalleghem, Thompson, Favre-Bulle, Rubinsztein-Dunlop and Scott.",
year = "2018",
month = jan,
day = "17",
doi = "10.3389/fnana.2017.00135",
language = "English",
volume = "11",
journal = "Frontiers in Neuroanatomy",
issn = "1662-5129",
publisher = "Frontiers Research Foundation",

}

RIS

TY - JOUR

T1 - Hypothalamic projections to the optic tectum in larval zebrafish

AU - Heap, Lucy A.

AU - Vanwalleghem, Gilles C.

AU - Thompson, Andrew W.

AU - Favre-Bulle, Itia

AU - Rubinsztein-Dunlop, Halina

AU - Scott, Ethan K.

N1 - Funding Information: We thank Rebecca Dunning for creating the PME-linker-MCS plasmid. We are grateful to Karl Deisseroth for providing the Channelrhodopsin-2(ET/TC) plasmid and Misha Ahrens for providing the HuC:H2B-GCaMP6s transgenic line. We thank Owen Randlett, Alexander Schier, and Florian Engert for providing the Z-Brain atlas prior to publication, as well as for assisting in Z-Brain analysis. We thank Jan Kaslin and members of the Scott laboratory for comments on the manuscript. Support was provided by the Australian Research Council Postgraduate Awards to LAH and AWT; an National Health and Medical Research Council (NHMRC) Project Grant (APP1066887), ARC Future Fellowship (FT110100887), a Simons Foundation Explorer Award (336331) and two ARC Discovery Project Grants (DP140102036 and DP110103612) to EKS; an ARC Discovery Project (DP140100753) to HR-D; a UQ Postgraduate Scholarship to IF-B; and an European Molecular Biology Organization (EMBO) Long-term Fellowship (ALTF 727-2014) to GCV. Imaging was performed at the Queensland Brain Institute’s Advanced Microscopy Facility, generously supported by the Australian Government through the ARC LIEF grant LE130100078. Publisher Copyright: © 2018 Heap, Vanwalleghem, Thompson, Favre-Bulle, Rubinsztein-Dunlop and Scott.

PY - 2018/1/17

Y1 - 2018/1/17

N2 - The optic tectum of larval zebrafish is an important model for understanding visual processing in vertebrates. The tectum has been traditionally viewed as dominantly visual, with a majority of studies focusing on the processes by which tectal circuits receive and process retinally-derived visual information. Recently, a handful of studies have shown a much more complex role for the optic tectum in larval zebrafish, and anatomical and functional data from these studies suggest that this role extends beyond the visual system, and beyond the processing of exclusively retinal inputs. Consistent with this evolving view of the tectum, we have used a Gal4 enhancer trap line to identify direct projections from rostral hypothalamus (RH) to the tectal neuropil of larval zebrafish. These projections ramify within the deepest laminae of the tectal neuropil, the stratum album centrale (SAC)/stratum griseum periventriculare (SPV), and also innervate strata distinct from those innervated by retinal projections. Using optogenetic stimulation of the hypothalamic projection neurons paired with calcium imaging in the tectum, we find rebound firing in tectal neurons consistent with hypothalamic inhibitory input. Our results suggest that tectal processing in larval zebrafish is modulated by hypothalamic inhibitory inputs to the deep tectal neuropil.

AB - The optic tectum of larval zebrafish is an important model for understanding visual processing in vertebrates. The tectum has been traditionally viewed as dominantly visual, with a majority of studies focusing on the processes by which tectal circuits receive and process retinally-derived visual information. Recently, a handful of studies have shown a much more complex role for the optic tectum in larval zebrafish, and anatomical and functional data from these studies suggest that this role extends beyond the visual system, and beyond the processing of exclusively retinal inputs. Consistent with this evolving view of the tectum, we have used a Gal4 enhancer trap line to identify direct projections from rostral hypothalamus (RH) to the tectal neuropil of larval zebrafish. These projections ramify within the deepest laminae of the tectal neuropil, the stratum album centrale (SAC)/stratum griseum periventriculare (SPV), and also innervate strata distinct from those innervated by retinal projections. Using optogenetic stimulation of the hypothalamic projection neurons paired with calcium imaging in the tectum, we find rebound firing in tectal neurons consistent with hypothalamic inhibitory input. Our results suggest that tectal processing in larval zebrafish is modulated by hypothalamic inhibitory inputs to the deep tectal neuropil.

KW - Hypothalamus

KW - Optogenetics

KW - SPIM (selective plane illumination microscopy)

KW - Superior colliculus

KW - Tectum

KW - Zebrafish

UR - http://www.scopus.com/inward/record.url?scp=85042434242&partnerID=8YFLogxK

U2 - 10.3389/fnana.2017.00135

DO - 10.3389/fnana.2017.00135

M3 - Journal article

AN - SCOPUS:85042434242

VL - 11

JO - Frontiers in Neuroanatomy

JF - Frontiers in Neuroanatomy

SN - 1662-5129

M1 - 135

ER -