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Tuesday, October 27, 2020 |
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Join us for a FREE Webinar
Multiphoton Autofluorescence Imaging of T-Cell Function
Tuesday, November 10, 2020 1:00 PM - 2:00 PM EST
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Sponsored by
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Immune cells, including T cells, have a range of functions depending on activation state and subtype. However, current methods to assess immune cell function use exogenous labels that are limiting for T-cell manufacturing and for time-course studies of immune cell behavior in tumors. Label-free optical imaging is an attractive solution.
In this webinar, Melissa Skala, Ph.D., will explain the use of multiphoton autofluorescence imaging of NAD(P)H and FAD, co-enzymes of metabolism, to monitor T-cell activation and function. Skala will demonstrate how this is a powerful method for label-free, nondestructive monitoring of T-cell metabolism within single cells. This method could inform new immunotherapy approaches for cancer, enable nondestructive assessment of T-cell manufacturing, and monitor in vivo T-cell behavior in mouse models of cancer.
Skala will reference her associated study in which T cells were isolated from the peripheral blood of human donors, activated or polarized to functional subsets, and subjected to tumor-like media (low pH, low glucose, high lactic acid). NAD(P)H and FAD fluorescence intensity and lifetime were monitored on a single-cell level over time. Logistic regression models and random forest models classified T cells according to activation state with 97% to 99% accuracy, and according to activation state (quiescent or activated) and subtype (CD3+CD8+ or CD3+CD4+) with 97% accuracy. From this study, significant differences in autofluorescence were observed between functional T-cell subsets in tumor-like media conditions compared to standard media conditions, reflecting metabolic adaptations to the tumor microenvironment.
The hardware, optics, and analytical algorithms of multiphoton autofluorescence imaging are readily integrated into a variety of quantitative imaging technologies, such as flow and image cytometry or intravital microscopy.
The webinar will conclude with a Q&A.
Who should attend:
All those investigating solutions for label-free, nondestructive imaging, especially for monitoring T cells in biomedical applications. Specialists and students in the life sciences seeking a better understanding of cellular imaging, specifically multiphoton fluorescence lifetime imaging.
About the presenter:
Skala received her B.S. in physics at Washington State University in 2002, her M.S. in biomedical engineering at the University of Wisconsin-Madison in 2004, and her Ph.D. in biomedical engineering at Duke University in 2007. Her postdoctoral training was also in Biomedical Engineering at Duke University, from 2007-2010. From 2010-2016, she was an assistant professor of biomedical engineering at Vanderbilt University. Since 2016 she has been an investigator at the Morgridge Institute for Research. She is also a professor of biomedical engineering at the University of Wisconsin-Madison. Her lab develops new methods to understand and combat cancer using photonics-based technologies.
Illustration credit: Alex Walsh.
This webinar is sponsored by Omega Optical, LLC. Omega Optical can provide standard or custom filters from UV to IR from prototype to production quantities in vision systems, life science, industrial, astronomy and defense applications. Omega Optical has designed over 100,000 custom optical filters and mirrors and shipped over 30 million since 1969.
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Date: Tuesday, November 10, 2020
Time: 1:00 PM - 2:00 PM EST
Space is limited. Reserve your Webinar seat now at: https://attendee.gotowebinar.com/register/2861878542908039949
After registering you will receive a confirmation email containing information about joining the Webinar.
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SYSTEM REQUIREMENTS
Operating System
Windows® 7 or later, Mac OS® X 10.9 or later, Linux®, Google ChromeTM OS
AndroidTM OS 5 or later, iOS® 10 or later
Web Browser
Google ChromeTM (most recent 2 versions)
Mozilla Firefox® (most recent 2 versions)
Mobile Devices
AndroidTM 5 or later
iPhone® 4S or later
iPad® 2 or later
Windows Phone® 8+, Windows® 8RT+
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