Microfluidic Capture Device for Simple, Cell Surface Marker-Based Quantification of Senescent CD8 T Cells
Biochip Journal, ISSN: 2092-7843, Vol: 18, Issue: 3, Page: 382-392
2024
- 3Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Captures3
- Readers3
Article Description
Among human CD8 T cells, senescent cells are marked by the expression of CD57. The frequency of senescent CD57CD8 T cells is significantly correlated with aging and age-associated disorders, and it can be measured by multi-color flow cytometry. However, multi-color flow cytometry presents challenges in terms of accessibility and requires significant resource allocation. Therefore, developing a rapid and straightforward method for quantifying CD57CD8 T cells remains a key challenge. This study introduces a microfluidic device composed of a PDMS microfluidic channel with a pre-modified glass substrate for anti-CD8 antibody immobilization. This design allows blood samples to flow through, enabling the selective capture of CD8 T cells while minimizing the required blood sample volume. This technology enables accurate and reliable quantification of CD57 cells among captured CD8 T cells through fluorescence image analysis. The ability of the device to easily quantify senescent CD57CD8 T cells is anticipated to contribute significantly to both immunological research and clinical applications.
Bibliographic Details
Springer Science and Business Media LLC
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