RT Journal Article
SR Electronic
T1 Spatial transcriptome sequencing of FFPE tissues at the cellular level
JF bioRxiv
FD Cold Spring Harbor Laboratory
SP 2020.10.13.338475
DO 10.1101/2020.10.13.338475
A1 Liu, Yang
A1 Enninful, Archibald
A1 Deng, Yanxiang
A1 Fan, Rong
YR 2020
UL http://biorxiv.org/content/early/2020/10/14/2020.10.13.338475.abstract
AB Formalin-fixed paraffin-embedded (FFPE) tissues are the most abundant archivable specimens in clinical tissue banks, but unfortunately incompatible with single-cell level transcriptome sequencing due to RNA degradation in storage and RNA damage in extraction. We developed an in-tissue barcoding approach namely DBiT-seq for spatially revolved whole transcriptome sequencing at cellular level, which required no tissue dissociation or RNA exaction, thus potentially more suited for FFPE samples. Herein, we demonstrated spatial transcriptome sequencing of embryonic and adult mouse FFPE tissue sections at cellular level (25μm pixel size) with high coverage (>1,000 genes per pixel). Spatial transcriptome of a E10.5 mouse embryo identified all major anatomical features in the brain and abdominal region. Integration with singlecell RNA-seq data for cell type identification indicated that most tissue pixels were dominated by single-cell transcriptional phenotype. Spatial mapping of adult mouse aorta, atrium, and ventricle tissues identified the spatial distribution of different cell types. Spatial transcriptome sequencing of FFPE samples at cellular level may provide enormous opportunities in a wide range of biomedical research. It may allow us to revisit retrospectively the huge resource of clinical tissue specimens to study human disease mechanisms for the discovery of tissue biomarkers and therapeutic targetsCompeting Interest StatementR.F. is scientific founder and advisor of IsoPlexis Singleron Biotechnologies and AtlasXomics. The interests of R.F. were reviewed and managed by Yale University Provost Office in accordance with the University conflict of interest policies.