Transcriptional analysis of islets of Langerhans from organ donors of different ages
Autor: | Oskar Skog, Anton Stenwall, Petr Volkov, Jonathan L.S. Esguerra, Olle Korsgren, Louise Granlund, Marcus Lundberg, Peter Seiron, Anders Hedin, Erik Renström |
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Jazyk: | angličtina |
Rok vydání: | 2021 |
Předmět: |
Male
Aging Physiology Gene Expression Biochemistry Transcriptome Endocrinology Medical Conditions Gene expression Insulin Secretion Medicine and Health Sciences Insulin Osteopontin Cell Cycle and Cell Division Child Cellular Senescence Laser capture microdissection Aged 80 and over Multidisciplinary geography.geographical_feature_category Organic Compounds Cell Cycle Monosaccharides Genomics Cell cycle Middle Aged Islet Type 2 Diabetes Chemistry Cell Processes Child Preschool Physical Sciences Medicine Female Transcriptome Analysis Research Article Senescence Adult endocrine system Adolescent Endocrine Disorders Science Carbohydrates Biology Andrology Islets of Langerhans Young Adult Downregulation and upregulation Genetics Diabetes Mellitus Humans Aged Diabetic Endocrinology geography Endocrine Physiology Gene Expression Profiling Organic Chemistry Chemical Compounds Infant Biology and Life Sciences Computational Biology Cell Biology Genome Analysis Hormones Glucose Metabolic Disorders biology.protein Physiological Processes Organism Development Developmental Biology |
Zdroj: | PLoS ONE, Vol 16, Iss 3, p e0247888 (2021) PLoS ONE |
ISSN: | 1932-6203 |
Popis: | Insulin secretion is impaired with increasing age. In this study, we aimed to determine whether aging induces specific transcriptional changes in human islets. Laser capture microdissection was used to extract pancreatic islet tissue from 37 deceased organ donors aged 1–81 years. The transcriptomes of the extracted islets were analysed using Ion AmpliSeq sequencing. 346 genes that co-vary significantly with age were found. There was an increased transcription of genes linked to senescence, and several aspects of the cell cycle machinery were downregulated with increasing age. We detected numerous genes not linked to aging in previous studies likely because earlier studies analysed islet cells isolated by enzymatic digestion which might affect the islet transcriptome. Among the novel genes demonstrated to correlate with age, we found an upregulation of SPP1 encoding osteopontin. In beta cells, osteopontin has been seen to be protective against both cytotoxicity and hyperglycaemia. In summary, we present a transcriptional profile of aging in human islets and identify genes that could affect disease course in diabetes. |
Databáze: | OpenAIRE |
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