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Grant: Discovery Grants Program - Individual

University of Saskatchewan

$62,000.00

Determining the biochemical mechanism of microbubble-mediated vascular permeability

FY 2023-24

Summary
One of the most exciting advancements in targeted drug delivery has been the use of ultrasound and microbubbles as a tool to cause blood vessels become leaky, allowing therapeutics to leave circulation at specific sites in the body. Microbubbles are a small (1-4 um), vascular restricted ultrasound contrast agent that consists of a lipid shell surrounding a gas core. When microbubbles come into contact with a focused ultrasound beam, they begin to expand and contract. Through some unknown biochemical mechanism, expansion and contraction of microbubbles causes the junctions in between the cells that make up the vasculature to break down for a short period of time, likely through the application of physical force. My goal is to develop a natural sciences and engineering research program based on determining what is the biochemical mechanism of how microbubbles can cause the vasculature to become leaky. It is my hypothesis that the rapid expansion and compression of microbubbles applies a physical strain to the vasculature, effectively stretching it and activating proteins that monitor and respond to mechanical stress. My trainees and I will investigate this by designing microbubbles and activating them with specially designed ultrasound pulse sequences within normal mouse vasculature. We will then investigate what gene networks are activated in the vascular endotheilal cells, observe changes in protein localization and activation, and step by step understand how cell signaling changes the vasculature response to expanding and contracting microbubbles. Once we understand this biochemical mechanism in normal vasculature, we can use it as a tool and apply it to other natural sciences and engineering fields, including leukocyte migration, where little is known about the role physical force applied to the vasculature plays. This funding will lead also result in the training of a minimum of 11 HQP within the next 5 years and provide them with an important and novel skillset (cell biology and ultrasound engineering) allowing them to become leaders of innovation within Canadian research.
Program
Discovery Grants Program - Individual
Location
Saskatchewan, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data

As published

Application id
RGPIN-2018-06505
Name nom
Machtaler, Steven
Department département
Medical Imaging
Organization id
16
Institution établissement
University of Saskatchewan
Province en
Saskatchewan
Province fr
Saskatchewan
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2023
Competition year année de concours
2018
Award amount
62000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
DISCOVERY RESEARCH
Group fr
RECHERCHE AXÉE SUR LA DÉCOUVERTE
Committee code
1501
Committee name en
Genes, Cells and Molecules
Committee name fr
Gènes, cellules et molécules
Area of application code
1211
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Medical and health sciences
Area of application fr
Sciences médicales et de la santé
Research subject code
5111
Research subject group en
Cell biology
Research subject group fr
Signal transduction
Research subject en
Biologie cellulaire
Research subject fr
Transduction de signal
Application title
Determining the biochemical mechanism of microbubble-mediated vascular permeability
Keyword
biochemical pathways; biophysics; cell biology; drug delivery; intercellular junctions; mechanotransduction; microbubbles; ultrasound
Application summary
One of the most exciting advancements in targeted drug delivery has been the use of ultrasound and microbubbles as a tool to cause blood vessels become leaky, allowing therapeutics to leave circulation at specific sites in the body. Microbubbles are a small (1-4 um), vascular restricted ultrasound contrast agent that consists of a lipid shell surrounding a gas core. When microbubbles come into contact with a focused ultrasound beam, they begin to expand and contract. Through some unknown biochemical mechanism, expansion and contraction of microbubbles causes the junctions in between the cells that make up the vasculature to break down for a short period of time, likely through the application of physical force. My goal is to develop a natural sciences and engineering research program based on determining what is the biochemical mechanism of how microbubbles can cause the vasculature to become leaky. It is my hypothesis that the rapid expansion and compression of microbubbles applies a physical strain to the vasculature, effectively stretching it and activating proteins that monitor and respond to mechanical stress. My trainees and I will investigate this by designing microbubbles and activating them with specially designed ultrasound pulse sequences within normal mouse vasculature. We will then investigate what gene networks are activated in the vascular endotheilal cells, observe changes in protein localization and activation, and step by step understand how cell signaling changes the vasculature response to expanding and contracting microbubbles. Once we understand this biochemical mechanism in normal vasculature, we can use it as a tool and apply it to other natural sciences and engineering fields, including leukocyte migration, where little is known about the role physical force applied to the vasculature plays. This funding will lead also result in the training of a minimum of 11 HQP within the next 5 years and provide them with an important and novel skillset (cell biology and ultrasound engineering) allowing them to become leaders of innovation within Canadian research.