Projects and Grants per year
Grants and Contracts Details
Description
The vascular endothelial cells lining blood vessels in humans are one of the principle
sites that become involved in inflammatory and proliferative responses to a diverse array
of human diseases. Microvascular homeostasis is thus a vital component of human
health; its inappropriate activation in response to inflammatory and angiogenic stimuli
can become a pathogenic component fueling the growth and spread of cancers, and
contributing to debilitating arthritis, age-related macular degeneration and multiple organ
failure associated with underlying diseases such as diabetes. On the other hand,
impaired angiogenesis is also equally pathogenic, and afflicts its victims by slowing
down wound healing and contributing to heart diseases and stroke. Collectively, given
the complexity of the angiogenesis signaling system, these major burdens of human
health that arise from dysregulation of blood vessel growth need to be addressed by a
more concerted effort in drug discovery. Biological assays that model the processes of
angiogenic diseases can assist the process of drug discovery and disease target
identification. However, currently few assays represent the complexity of the diseased
microvasculature as they typically focus on one pathogenic mechanism/pathway. With
this in mind, we propose to continue the development of a high content high throughput
screening (HC-HTS) vascular patterning assay, which we have recently validated as
drug screening tool through a previously funded NIH Roadmap Initiative R21 grant. In
this R01 proposal, we plan to extend the scale and scope of the three dimensional
endothelial cell sprouting assay (3D-ECSA) to promote its adoption for the HTS
paradigm. Our innovative approaches bring in 1) modern automated robotic systems that
allow us to improve efficiency and standardize production of spheroids, 2) high content
image analysis software to use with 3D-ECSA under HTS conditions, and 3)
development of a pilot scale chemical library focused on the immunoproteosome as a
chemical enabling tool towards validation of the 3D-ECSA. The successful
accomplishments of these goals will not only afford us a valuable tool for large scale
biology, but will help bring forward a technology advancement to identify new classes of
chemical probes of protein function and drug leads for life saving therapeutics.
Status | Finished |
---|---|
Effective start/end date | 7/1/08 → 9/30/10 |
Funding
- National Cancer Institute
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Projects
- 1 Finished
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Novel Modular Vascular Patterning Assay for HTS
Mohan, R., Kim, K., Lau, D. & Hassebrook, L.
7/1/08 → 9/30/10
Project: Research project