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2010 - Undergraduate Research, Scholarship and Creative Activity

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aspect of the process involves developing<br />

synthesis conditions for ZnO <strong>and</strong> the in-situ<br />

monitoring (via atomic force microscopy) of<br />

ZnO synthesized on a Au wafer (1) at low<br />

temperatures <strong>and</strong> under neutral solution<br />

conditions. The second aspect involves synthesizing<br />

ZnO (1) in the presence of amino acids<br />

with different ―R‖ groups (hydrophilic,<br />

hydrophobic, acidic <strong>and</strong> basic), (2) at low<br />

temperatures, <strong>and</strong> (3) a range of pH‘s in order to<br />

exert kinetic control of the crystal growth<br />

process. Initial results show that L-Histidine <strong>and</strong><br />

L-Cysteine have significant effects on crystal<br />

morphology <strong>and</strong> are subsequently studied. This<br />

research will help us further utilize the mineralspecific<br />

interactions that occur in nature so that<br />

we can synthesize advanced functional materials<br />

in a more cost efficient <strong>and</strong> environmentally<br />

friendly way.<br />

Using in vivo <strong>and</strong> in vitro models to identify<br />

the consequences of manipulating chemokine<br />

<strong>and</strong> immune response genes during CNS<br />

neuroinflammation<br />

Tokunbo Ayeni, Biology<br />

Amelia Lipscomb, Neuroscience<br />

Contributors: Joe Elsissy, Angie Garcia<br />

Mentor: Monica J. Carson<br />

Division of Biomedical Sciences<br />

Interactions between the central nervous system<br />

(CNS) <strong>and</strong> the immune system are essential to<br />

maintain optimal brain function during health<br />

<strong>and</strong> after injury or infection by pathogens.<br />

Chronic <strong>and</strong>/or dysregulated interactions<br />

between the CNS are hypothesized to contribute<br />

to the onset <strong>and</strong> progression of multiple<br />

neurologic disorders including Alzheimer‘s<br />

disease. In our lab, we are focusing on the role<br />

of two molecules: 1) CCL21, a chemoattractant<br />

molecule that recruits <strong>and</strong> retains T cells <strong>and</strong><br />

dendritic cells in the CNS, <strong>and</strong> 2) Tmem176b, a<br />

tetraspan membrane protein that is expressed by<br />

macrophages in the CNS during acute neuroinflammatory<br />

conditions that successfully<br />

resolve. Our hypothesis is that failure to express<br />

sufficient Tmem176b may contribute to the<br />

transition of beneficial acute inflammation to<br />

detrimental chronic inflammation. We can test<br />

whether Tmem176b expression is correlative or<br />

causative in the resolution of neuroinflammation<br />

by testing in vitro if Tmem176b alters<br />

macrophage activation <strong>and</strong> by testing in vivo. In<br />

vitro, we have cultured two types of macrophage<br />

cell lines. RAW cells which are immortalized<br />

peripheral macrophage cells <strong>and</strong> BV-2 cells<br />

which are immortalized microglia. Microglia<br />

are a type of macrophage that is specific to the<br />

CNS. We have prepared maxipreps of<br />

Tmem176b expression plasmids that when transfected<br />

into RAW <strong>and</strong> BV-2 cells results in the<br />

over expression of Tmem176b. Because the<br />

plasmid also contains the reporter molecule,<br />

green-fluorescent protein (GFP), we can detect<br />

the cells which were successfully transfected.<br />

Using this tools, we have discovered that overexpression<br />

of Tmemb176b promotes apoptosis<br />

of both macrophage <strong>and</strong> microglia-like cells. We<br />

can also test the function of Tmem176b in vivo<br />

by overexpressing Tmem176b in mouse models<br />

where we selectively promote inflammation by<br />

transgenically manipulating expression of<br />

CCL21. For this purpose we are breeding <strong>and</strong><br />

genotyping four types of mice: a) wild-type<br />

expression of CCL21 throughout the body, b)<br />

lack expression of CCL21 (plt/plt CCL21<br />

knock-out mice), c) selective expression in the<br />

pancreas (Ins-CCL21 transgenic mice), <strong>and</strong> d)<br />

selective expression in the brain (GFAP-CCL21<br />

transgenic). As part of this portion of our<br />

studies, we have learned to use PCR based<br />

methodologies to determine the presence or<br />

absence of specific endogenous genes (CCL21)<br />

or transgenes (Ins-CCL21 <strong>and</strong> GFAP-CCL21).<br />

Issues of Drinking Water Quality in India<br />

Jennifer Barr, Anthropology/<strong>Creative</strong> Writing<br />

Mentors: Sally Ness, Department of<br />

Anthropology<br />

David Cwiertny, Department of Environmental<br />

Engineering<br />

Around 37.7 million Indians are afflicted with<br />

waterborne diseases each year. Thirty percent<br />

(30%) of urban households <strong>and</strong> 90% of rural<br />

households in India rely entirely on untreated<br />

drinking water, depending on surface <strong>and</strong><br />

ground water sources contaminated by the<br />

results of poor sanitation <strong>and</strong> waste disposal.<br />

Poor water quality has had far-reaching<br />

Fourth Annual UCR Symposium for <strong>Undergraduate</strong> <strong>Research</strong>, <strong>Scholarship</strong> <strong>and</strong> <strong>Creative</strong> <strong>Activity</strong><br />

20

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