Novel epigenetic clock for fetal brain development predicts prenatal age for cellular stem cell models and derived neurons

Autor: Akshay Bhinge, Emma Dempster, Emma L Cope, Grainne M. McAlonan, Leo W. Perfect, Eilis Hannon, Aaron R. Jeffries, Grant W. A. Neilson, Jennifer Imm, Nicholas D. Allen, Jonathan Mill, Nicholas John Bray, Katie Lunnon, Jack Price, Gemma Shireby, Emma Walker, Leonard C. Steg, Deepak Srivastava, Kimberley M Jones, Robert Flynn, Ehsan Pishva, Seema C. Namboori, Joe Burrage, Jonathan P. Davies, Alice Franklin
Přispěvatelé: RS: MHeNs - R3 - Neuroscience, Psychiatrie & Neuropsychologie
Jazyk: angličtina
Rok vydání: 2021
Předmět:
Zdroj: Molecular Brain, Vol 14, Iss 1, Pp 1-11 (2021)
Molecular Brain
Molecular Brain, 14(1):98. BioMed Central
ISSN: 1756-6606
Popis: Induced pluripotent stem cells (iPSCs) and their differentiated neurons (iPSC-neurons) are a widely used cellular model in the research of the central nervous system. However, it is unknown how well they capture age-associated processes, particularly given that pluripotent cells are only present during the earliest stages of mammalian development. Epigenetic clocks utilize coordinated age-associated changes in DNA methylation to make predictions that correlate strongly with chronological age. It has been shown that the induction of pluripotency rejuvenates predicted epigenetic age. As existing clocks are not optimized for the study of brain development, we developed the fetal brain clock (FBC), a bespoke epigenetic clock trained in human prenatal brain samples in order to investigate more precisely the epigenetic age of iPSCs and iPSC-neurons. The FBC was tested in two independent validation cohorts across a total of 194 samples, confirming that the FBC outperforms other established epigenetic clocks in fetal brain cohorts. We applied the FBC to DNA methylation data from iPSCs and embryonic stem cells and their derived neuronal precursor cells and neurons, finding that these cell types are epigenetically characterized as having an early fetal age. Furthermore, while differentiation from iPSCs to neurons significantly increases epigenetic age, iPSC-neurons are still predicted as being fetal. Together our findings reiterate the need to better understand the limitations of existing epigenetic clocks for answering biological research questions and highlight a limitation of iPSC-neurons as a cellular model of age-related diseases. Supplementary Information The online version contains supplementary material available at 10.1186/s13041-021-00810-w.
Databáze: OpenAIRE
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