This week I finished my data collection! Getting 50 subjects seemed easy-ish at first but it actually turned out to be a lot harder than I thought. I finished Wednesday night and Thursday was one of the busiest days I’ve had so far. Dr. Peretz visited me and took me out to lunch (!!!) and then I got to show her around my lab and introduce her to Nick (the postdoc) and Dr. Lewis (even though we had to interrupt his meeting to say hi). Then I got to meet with Dr. Lewis and Nick and we discussed what the next steps of data analysis would be. We ended up talking for over an hour which was great because they both helped me a lot and genuinely wanted me to understand what I was doing. We worked together to categorize the questions in the surveys into “social behaviors” and “non-social behaviors” and then we discussed how to give each individual a score for how “social” they are. Kinda hard to explain without showing it but basically as I sort of explained in an earlier blog post each answer choice corresponds to a number 1-4 so after I enter all the data and add up the numbers, the lower the score, the more “social” an individual seems to be. After this, we discussed how I need to go through all the data again and expand on some of the questions so that’s what I’ll be doing for the next few days at least. After we get all of that sorted, we’ll be able to more easily look at the data and what it all means. Dr. Lewis is really understanding of the fact that I have to do a whole presentation about this in the fall so he said after I leave, they’ll continue the work and I can meet with him in the fall to get all the data together for a presentation.
As mentioned in my previous blog, I have been awaiting ligament, menisci, and cartilage tissue from a canine or human knee joint for (interleukin) IL-1B tissue culture. IL-1B is an inflammatory cytokine that has been proven to increase rates of tissue degeneration and osteoarthritis development in the Thompson Lab. Dr. Stoker wants me to experiment with different types of knee tissues in a co-culture with varying levels of this cytokine to determine its effects on the entire knee joint. This co-culture uses an insert permeable to the media to separate the two tissue samples from physical contact, while allowing them to share the same media. This creates an extremely accurate model for knee tissues in their native environment due to their exposure to the same synovial fluid in the joint. This model would then be treated with the IL-1B and cultured for 21 days. During these 21 days, the media would be collected every three days for biomarker evaluation at the end of the stu...
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