Research interest:
I am looking for new ligands of voltage-gated calcium channels (VGCCs)
in the brain synapse. At the neuromuscular junction, VGCCs interact
with laminin beta 2, and the interaction is involved in the formation
and/or maintenance of the active zone. However, laminin beta 2 is not
present at the brain synapse. We speculate that protein-protein interaction
including VGCCs participate in the formation and/or maintenance of
the active zone at the brain synapse.
Rajat Sandhir
Senior Scientist
Mentor: Nancy Berman
email: rsandhir@kumc.edu
My research involves investigating molecular mechanisms involved in
worse outcomes in aged following traumatic brain injury (TBI). We have
observed exacerbated glial response and higher expression of pro- inflammatory
cytokines and chemokines in aged mice compared to adult mice which may
be responsible for poor outcome after brain injury in elderly. We are
currently trying to role transcription factors in differential response
of the aged brain to TBI. In addition we are investigating the role
of metalloproteinases 2 and 9 in increased BBB permeability in the aged
brain following TBI.
Research interests: Cux-1 is the murine homologue of the Drosophila gene Cut, which is required for cellular differentiation in several tissues including the wing margin and Malphigian tubule. Mammalian cut proteins function as cell cycle-dependent transcriptional repressors in proliferating cells. Targets of Cux-1 repression include the cyclin kinase inhibitors p21 and p27. However, little is known about the regulation of Cux-1. In Drosophila, multiple genetic interactions between Cut and the Notch and Wingless signaling pathways occur during wing development. For the past couple of years , I have been interested in determining whether Cux-1 regulation by the Notch signaling pathway is conserved in mammals. Preliminary studies using immunohistocemistry and immunoprecipitations show that Cux-1 could indeed be regulated by notch pathway and to explore this would be my future target.
Research interests: I am studying kidney development and disease using a mouse model of human Alport syndrome. This mouse has a deletion in the type IV collagen alpha 3 chain found in the glomerular basement membrane of the kidney. Mice lacking the alpha 3 chain of type IV collagen develop glomerulosclerosis and eventually die of end stage renal failure. I am analyzing glomerular RNA from these mice using DNA microarray to identify genes which are misregulated during the pathogenesis of the disease.
Veronica Zaga-Clavellina, Ph.D.
Postdoctoral Fellow
Mentor: Dr. Joan S Hunt
Immunologic privilege and innate immunology in pregnancy. Immunologic
role of human chorioamnion and placenta in the normal and abnormal
pregnancies.