Single-Cell Transcriptome Profiling of Human Pancreatic Islets in Health and Type 2 Diabetes
We used single-cell RNA-sequencing to generate transcriptional profiles of endocrine and exocrine cell types of the human pancreas. Pancreatic tissue and islets were obtained from six healthy and four T2D cadaveric donors. Islets were cultured and dissociated into single-cell suspension. Viable individual cells were distributed via fluorescence-activated cell sorted (FACS) into 384-well plates containing lysis buffer. Single-cell cDNA libraries were generated using the Smart-seq2 protocol. Gene expression was quantified as reads per kilobase transcript and per million mapped reads (RPKM) using rpkmforgenes. Bioinformatics analysis was used to classify cells into cell types without knowledge of cell types or prior purification of cell populations. We revealed subpopulations in endocrine and exocrine cell types, identified genes with interesting correlations to body mass index (BMI) in specific cell types and found transcriptional alterations in T2D. Complementary whole-islet RNA-seq data have also been deposited at ArrayExpress under accession number E-MTAB-5060 (http://www.ebi.ac.uk/arrayexpress/experiments/E-MTAB-5060).
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Atlas
Analysis Portals
Project Label
Healthy and type 2 diabetes pancreasSpecies
Homo sapiens
Sample Type
specimens
Anatomical Entity
pancreas
Organ Part
islet of Langerhans
Selected Cell Types
Unspecified
Disease Status (Specimen)
Unspecified
Disease Status (Donor)
Development Stage
human adult stage
Library Construction Method
Smart-seq2
Nucleic Acid Source
single cell
Paired End
falseAnalysis Protocol
MultiSampleSmartSeq2_v2.2.6, SmartSeq2SingleSample_v5.1.5File Format
Cell Count Estimate
3.5kDonor Count
10