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| Funder | NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE |
|---|---|
| Recipient Organization | University of Michigan At Dearborn |
| Country | United States |
| Start Date | Sep 01, 2024 |
| End Date | Aug 31, 2027 |
| Duration | 1,094 days |
| Number of Grantees | 1 |
| Roles | Principal Investigator |
| Data Source | NIH (US) |
| Grant ID | 10973503 |
Project summary/abstract The neurovascular unit (NVU) is responsible for the maintenance of blood-brain barrier (BBB) integrity, cerebral homeostasis, and control of cerebral blood flow. Evidence indicates that traumatic brain injury (TBI) alters the NVU functions and impairs the integrity of BBB; however, the mechanism is still poorly understood.
Cells have been discovered to possess phenotype-dependent intrinsic chirality, which not only reflects cellular behaviors but also influences tissue/organ morphogenesis and physiological functions. The goal of this proposal is to evaluate the TBI-induced changes in cell chirality and cell-cell interactions of microglia, neurons,
and brain microvascular endothelial cells (BMECs) within the NVU. We use a pre-established TBI animal model, combined with novel biological and engineering techniques, to complete the aims of the proposed project. Aim 1 determines the chirality, polarization, and organelles positioning of microglia and neurons, as
well as the physical interactions between microglia and neurons after TBI. Aim 2 examines the TBI-induced changes in the chirality of BMECs and the interaction between microglia and BMECs. Results obtained from this project will reveal the relationship between cell chirality and cell-cell interactions of microglia, neurons, and
BMECs within the NVU. Thus, the accomplishment of this project will provide novel knowledge on cell chirality regulation and mechanisms of NVU function, which will further set the foundation for developing cell-specific therapeutics that can be translated to various neurological disorders.
University of Michigan At Dearborn
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