FIN-Seq: transcriptional profiling of specific cell types from frozen archived tissue of the human central nervous system

Author:

Amamoto Ryoji12ORCID,Zuccaro Emanuela1,Curry Nathan C1,Khurana Sonia1,Chen Hsu-Hsin1,Cepko Constance L2,Arlotta Paola13

Affiliation:

1. Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA

2. Department of Genetics and Ophthalmology, Howard Hughes Medical Institute, Blavatnik Institute, Harvard Medical School, Boston, MA 02115, USA

3. Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA

Abstract

AbstractThousands of frozen, archived tissue samples from the human central nervous system (CNS) are currently available in brain banks. As recent developments in RNA sequencing technologies are beginning to elucidate the cellular diversity present within the human CNS, it is becoming clear that an understanding of this diversity would greatly benefit from deeper transcriptional analyses. Single cell and single nucleus RNA profiling provide one avenue to decipher this heterogeneity. An alternative, complementary approach is to profile isolated, pre-defined cell types and use methods that can be applied to many archived human tissue samples that have been stored long-term. Here, we developed FIN-Seq (Frozen Immunolabeled Nuclei Sequencing), a method that accomplishes these goals. FIN-Seq uses immunohistochemical isolation of nuclei of specific cell types from frozen human tissue, followed by bulk RNA-Sequencing. We applied this method to frozen postmortem samples of human cerebral cortex and retina and were able to identify transcripts, including low abundance transcripts, in specific cell types.

Funder

National Institutes of Health

Howard Hughes Medical Institute

Publisher

Oxford University Press (OUP)

Subject

Genetics

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