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Grant: Research Tools and Instruments - Category 1 (<$150,000)

University of British Columbia

$149,075.00

A combined epifluorescent and confocal imaging system

EF 2014-15

Résumé
Microscopic imaging is vital to my laboratory's research programme. Our work is focused on normal structure and function of neural cells (neurons and supporting cells known as glia), how cells of the nervous system react to injury, and how potential treatments can halt damage or promote repair. For example, we have discovered a new sub-cellular structure (organelle) which we have named the loukoumasome (doughnut-like body), present in some nerve cells of the peripheral nervous system. Current work is aimed in part at determining the loukoumasome's composition in order to glean information about its function. In another line of investigation, we have found that cells of the peripheral nervous system grow new nerve fibres in response to spinal cord injury, possibly mediating some of the important secondary consequences of this debilitating condition such as pain and abnormal cardiovascular control. In another project we are investigating how an oxygen sensing protein is responsible for some of the responses of glial cells to spinal cord injury which prevent regeneration and contribute to neuropathic pain.All of this work requires high-resolution light (fluorescence) microscopy to investigate the fine details of e.g. loukoumasome structure, newly-grown nerve fibres and their contacts, and interactions between different types of glia, and between glia and neurons. This application is for a state-of-the-art imaging system (microscope, camera, computer and software) which will be able to operate not only at lower magnification for rapid image acquisition and processing (standard epifluorescence; this capability will replace an older defunct imaging system in my laboratory), but also at high magnification and high resolution (laser scanning confocal microscopy) to investigate the three-dimenstional structure of nerve cells and fibres, glial interactions, and the structure and contents of various cells of the central and peripheral nervous systems. This dual imaging system will allow us to solve mysteries about the basic workings of the nervous system and how it might be repaired.
Programme
Research Tools and Instruments - Category 1 (<$150,000)
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data

Tel que publié

Application id
472841-2015
Name nom
Ramer, Matthew
Department département
International Collaboration on Repair Discoveries (ICORD)
Organization id
2
Institution établissement
University of British Columbia
Province en
British Columbia
Province fr
Colombie-Britannique
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2014
Competition year année de concours
2015
Award amount
149075
Program id
EQPEQ
Program name en
Research Tools and Instruments - Category 1 (<$150,000)
Program name fr
Outils et instruments de recherche - catégorie 1 (<150 000$)
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
1501
Committee name en
Genes, Cells and Molecules
Committee name fr
Gènes, cellules et molécules
Area of application code
1201
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Life sciences (including biotechnology)
Area of application fr
Sciences de la vie (y compris biotechnologie)
Research subject code
5100
Research subject group en
Cell biology
Research subject group fr
Biologie cellulaire
Research subject en
Cell biology
Research subject fr
Biologie cellulaire
Partie
1
Nb partie
1
Application title
A combined epifluorescent and confocal imaging system
Keyword
NSERC
Application summary
Microscopic imaging is vital to my laboratory's research programme. Our work is focused on normal structure and function of neural cells (neurons and supporting cells known as glia), how cells of the nervous system react to injury, and how potential treatments can halt damage or promote repair. For example, we have discovered a new sub-cellular structure (organelle) which we have named the loukoumasome (doughnut-like body), present in some nerve cells of the peripheral nervous system. Current work is aimed in part at determining the loukoumasome's composition in order to glean information about its function. In another line of investigation, we have found that cells of the peripheral nervous system grow new nerve fibres in response to spinal cord injury, possibly mediating some of the important secondary consequences of this debilitating condition such as pain and abnormal cardiovascular control. In another project we are investigating how an oxygen sensing protein is responsible for some of the responses of glial cells to spinal cord injury which prevent regeneration and contribute to neuropathic pain.All of this work requires high-resolution light (fluorescence) microscopy to investigate the fine details of e.g. loukoumasome structure, newly-grown nerve fibres and their contacts, and interactions between different types of glia, and between glia and neurons. This application is for a state-of-the-art imaging system (microscope, camera, computer and software) which will be able to operate not only at lower magnification for rapid image acquisition and processing (standard epifluorescence; this capability will replace an older defunct imaging system in my laboratory), but also at high magnification and high resolution (laser scanning confocal microscopy) to investigate the three-dimenstional structure of nerve cells and fibres, glial interactions, and the structure and contents of various cells of the central and peripheral nervous systems. This dual imaging system will allow us to solve mysteries about the basic workings of the nervous system and how it might be repaired.