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Jalalvand, E., Alvelid, J., Coceano, G., Edwards, S., Robertson, B., Grillner, S. & Testa, I. (2022). ExSTED microscopy reveals contrasting functions of dopamine and somatostatin CSF-c neurons along the lamprey central canal. eLIFE, 11, Article ID e73114.
Open this publication in new window or tab >>ExSTED microscopy reveals contrasting functions of dopamine and somatostatin CSF-c neurons along the lamprey central canal
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2022 (English)In: eLIFE, E-ISSN 2050-084X, Vol. 11, article id e73114Article in journal (Refereed) Published
Abstract [en]

Cerebrospinal fluid-contacting (CSF-c) neurons line the central canal of the spinal cord and a subtype of CSF-c neurons expressing somatostatin, forms a homeostatic pH regulating system. Despite their importance, their intricate spatial organization is poorly understood. The function of another subtype of CSF-c neurons expressing dopamine is also investigated. Imaging methods with a high spatial resolution (5-10 nm) are used to resolve the synaptic and ciliary compartments of each individual cell in the spinal cord of the lamprey to elucidate their signalling pathways and to dissect the cellular organization. Here, light-sheet and expansion microscopy resolved the persistent ventral and lateral organization of dopamine- and somatostatin-expressing CSF-c neuronal subtypes. The density of somatostatin-containing dense-core vesicles, resolved by stimulated emission depletion microscopy, was shown to be markedly reduced upon each exposure to either alkaline or acidic pH and being part of a homeostatic response inhibiting movements. Their cilia symmetry was unravelled by stimulated emission depletion microscopy in expanded tissues as sensory with 9 + 0 microtubule duplets. The dopaminergic CSF-c neurons on the other hand have a motile cilium with the characteristic 9 + 2 duplets and are insensitive to pH changes. This novel experimental workflow elucidates the functional role of CSF-c neuron subtypes in situ paving the way for further spatial and functional cell-type classification.

Place, publisher, year, edition, pages
eLIFE SCIENCES PUBL LTD, 2022
Keywords
STED, light-sheet, cilia structure, Spinal cord, Mouse, Lamprey
National Category
Neurosciences
Identifiers
urn:nbn:se:kth:diva-309046 (URN)10.7554/eLife.73114 (DOI)000751630600001 ()35103591 (PubMedID)2-s2.0-85125612750 (Scopus ID)
Note

QC 20220308

Available from: 2022-03-08 Created: 2022-03-08 Last updated: 2023-02-08Bibliographically approved
Jalalvand, E., Alvelid, J., Coceano, G., Edwards, S., Robertson, B., Grillner, S. & Testa, I.ExSTED microscopy reveals contrasting functions of dopamine and somatostatin CSF-c neurons along the central canal.
Open this publication in new window or tab >>ExSTED microscopy reveals contrasting functions of dopamine and somatostatin CSF-c neurons along the central canal
Show others...
(English)Manuscript (preprint) (Other academic)
Abstract [en]

The spatial location of cerebrospinal fluid contacting (CSF-c) neurons enables important regulatory homeostatic functions regarding pH and motion control. Their intricate organization, facing the central canal and extending across the spinal cord, in relation to specific subtypes is poorly understood. This calls for imaging methods with a high spatial resolution (5-10 nm) to resolve the synaptic and ciliary compartments of each individual cell to elucidate their signalling pathways and enough throughput to dissect the cellular organization. Here, light-sheet and expansion microscopy resolved the persistent ventral and lateral organization of dopamine and somatostatin CSF-c neuronal types.

The number of somatostatin-containing dense core vesicles, resolved by STED microscopy, was shown to be markedly reduced upon each exposure to alkaline or acidic pH inhibiting any movement as part of a homeostatic response. Their cilia symmetry was unravelled by ExSTED as sensory in contrast with the motile one found in the dopaminergic ph insensitive neurons. This novel experimental workflow elucidates the functional role of CSF-c neuron subtypes in situ paving the way for further spatial and functional cell type classification.

Keywords
STED, microscopy, nanoscopy, neuroscience, lamprey
National Category
Biophysics Neurosciences
Research subject
Biological Physics
Identifiers
urn:nbn:se:kth:diva-305050 (URN)10.1101/2021.08.17.456595 (DOI)
Funder
Swedish Foundation for Strategic Research , FFL15-0031Göran Gustafsson Foundation for promotion of scientific research at Uppala University and Royal Institute of TechnologyScience for Life Laboratory, SciLifeLab
Note

QC 20211124

Available from: 2021-11-19 Created: 2021-11-19 Last updated: 2025-02-20Bibliographically approved
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ORCID iD: ORCID iD iconorcid.org/0000-0003-4759-3301

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