Author:
Fortmann Seth D.,Frey Blake F.,Hanumanthu Vidya Sagar,Liu Shanrun,Goldsborough Andrew,Kilchrist Kameron V.,Ferrell P. Brent,Weaver Casey T.,Grant Maria B.,Welner Robert S.
Abstract
SUMMARYSingle-cell RNA-sequencing (scRNA-seq) presents an opportunity to deconstruct cellular networks but is limited by the loss of biological information, includingin vivocellular states and phospho-signaling. Herein, we present fixation before dissociation using a deep eutectic solvent (DES), which preserves multiple domains ofin vivobiological data, including morphology, RNA, proteins, and post-translational modifications. In scRNA-seq of viable versus DES bone marrow, dissociation induced global stress responses, immune and stromal cell activation, and loss of highly sensitive cell populations, which were prevented with DES. Further, we introduce a validated and flexible method for performing intracellular CITE-seq in DES-fixed cells. Leveraging this approach during Th17 T cell stimulation allowed the simultaneous quantification of transcriptomes and four phosphorylated proteins, leading to the identification of a hyperactivated state in p-ERK/p-FOS double positive cells, which we experimentally validated. We anticipate that DES-based fixatives will allow the accurate reconstruction ofin vivocellular networks and uncover cooperativity amongst intracellular pathways.
Publisher
Cold Spring Harbor Laboratory
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