TempO-Seq Gene Expression Profiling of Intracellular Stained FACS Sorted Cells - PROJECT SUMMARY
We propose to develop and validate an intracellular stained Fluorescence Activated Cell Sorter Templated
Oligonucleotide Sequencing gene profiling assay, icsFACS/TempO-Seq, addressing an unmet need by
enabling low-cost, quantitative gene expression analysis of fixed, permeabilized, and intracellular stained and
sorted cells (a method used to purify many different functionally important and rare subsets of cells), including
single cells, on both the FACSAria and benchtop BD FACSMelody, Sony SH800, and BioRad S3e sorters. We
successfully demonstrated feasibility in Phase I, developing two protocols for profiling single FACS sorted
cells. In addition, we were able to demonstrate novel observations regarding the stochastic expression of
genes at the single cell level due to the performance of the assay and virtual absence of background signal so
that true ”0” expression levels of genes that were off in single cells at the time of fixation could be measured. In
Phase II we will optimize these protocols and validate a menu of assays for human and mouse – a whole
transcriptome assay, a surrogate assay, a panel comprised of the surrogate assay plus immune response
genes for both mouse and human, and a panel comprised of host response genes, HIV-1 viral RNA and DNA.
We will demonstrate utility to generate time course data of normal T-cells activated ex vivo for subsets and
single cells within those subsets. Finally, we will generate novel data in the course of demonstrating utility in a
mouse model carried out in collaboration with an expert consultant, and by data obtained from HIV-1 patients
in a ¿-test client arrangement with an expert in HIV research. In the mouse model we will profile GC B cells
undergoing programmed rounds of hypermutation and selection (proliferation) and monitor subset purity in a
notoriously coalescing surface-staining phenotype. In the human model, the ¿-test client will profile FACS
sorted samples from HIV-1 infected patients undergoing triple antiretroviral therapy (ART) to characterize the
host RNA response and HIV-1 provirus DNA and viral mRNA harbored within the CD4+ T memory cell
compartments and enumerate residual HIV+ CD4+ T cells. The assay used will include measurement of viral
RNA and DNA at the same time as host genes. The icsFACS/TempO-Seq protocols and assays developed
and validated will address unmet needs in flow cytometry and immunology across a growing range of
diseases, including infectious diseases, inflammation, cancer, stroke, and Alzheimer’s to name a few.
Validation for both the FACSAria and benchtop sorters will address the needs of core labs and their clients and
investigators who choose to use, or require the specialized single cell performance, of these benchtop sorters.
It also lays the groundwork for the development of diagnostic assays on these benchtop sorter platforms using
icsFACS/TempO-Seq.