Author: Barrett Nehilla

HUVEC express vacuoles on transwells

My goal for this experiment was to see whether vacuoles form in primary cells.  If they did, this makes the case that the results with bEnd3 are more physiologically relevant since primary cells are better models of in vivo behavior. 

Posted in NRG

Vacuole inhibition by bafilomycin A1 (trial 2)

I wanted to confirm my results from this previous post.  Here, I used lower concentrations of bafilomycin (10, 25 and 50nM) in growth media.  Everything else was the same (except the cells were 1 passage older). The results are the

Posted in NRG

Pharmacological Inhibition of Vacuole Formation

I’ve been trying to convince myself that the black holes seen in endothelial cells that we’ve been calling vacuoles are actually vacuoles.  The first set of experiments involved staining cells with TAMRA, a fluid-phase marker which should get pinocytosed into

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AFM of film roughnesses

Chris asked me to do some scans of samples last week but I didn’t have time to get to them.  I was able to scan them today since I was setting the AFM up for my class anyway. I took

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Cells on squares vs. slits

Last week, I finished up an initial experiment to investigate whether pnc-Si membrane geometry affects cell morphology.  To do this, I used a mask with 2×2 arrays of different size squares and also samples with 4 slits of different lengths

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Permeability causes vacuole formation

Another one of the questions I’ve been trying to answer with regard to endothelial cell vacuoles is whether membrane mechanics or permeability drive vacuole expression.  I’ve thought of several experimental designs to test this that haven’t worked (i.e., using very

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TAMRA labeling of vacuoles

One of the ongoing efforts with endothelial cell culture on pnc-Si is to confirm that the holes in these cells are actually vacuoles.  In my last post, I tried to do this with FITC-Dextran and TMRIA with indefinite results.  I

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Cells in free space

Tom recently designed a wafer with 1cm2 chips containing a 2×2 array of 1mm2 square membrane windows that fit on 384-well plates.  I wanted one of these chips to get a preliminary data image for my R21 application.  Instead, I

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TEER of 1st 2 cocultures

My previous 2 posts on co-cultures presented images but I also tracked the TEER in these experiments.  This post shows that data. The top 2 graphs are from the 1st co-culture experiment – the bottom graph is from the second

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BBB co-culture (2)

In my last post (the first co-culture), I showed that bEnd3 cells exhibited a different morphology when they were co-cultured.  I also decided that I would reverse the orientation of the co-culture in order to better visualize the endothelial barrier. 

Posted in NRG
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