Aging CellCell BiologyPeer-reviewed journal article
TELOMERASE DEPLETION ACCELERATES AGEING OF THE ZEBRAFISH BRAIN
Raquel Rua MartinsiD, Savandara BesseiD, Pam S. EllisiD, Rabia SeviliD, Naomi HartoppiD, Catherine PurseiD, Georgia Everett‐Brown, Owain EvansiD, Nadiyah Mughal, Mina H. F. Wahib, Zerkif Yazigan, Samir MorsliiD, Ada Jiménez-GonzáleziD, Andrew J. GriersoniD, Heather MortiboysiD, Chrissy L. HammondiD, Michaël ReraiD, Catarina Martins HenriquesiD
Abstract
Decreased telomerase expression, telomere shortening, senescence-associated markers and inflammation have all been independently observed in the ageing brain and associated with disease. However, causality between limited telomerase expression and brain senescence and neuro-inflammation in the natural ageing setting is yet to be established. Here, we address these questions using the zebrafish as an ageing model which. Akin to humans, zebrafish display premature ageing and death in the absence of telomerase and where telomere shortening is a driver of cellular senescence. Our work shows for the first time that telomerase deficiency (tert-/-) accelerates key hallmarks of ageing identified in the Wild Type (WT) zebrafish brain at transcriptional, cellular, tissue and functional levels. We show that telomerase depletion accelerates ageing-associated transcriptomic changes associated with dysregulation of stress response and immune genes. These are accompanied by accelerated in situ accumulation of senescence-associated markers and inflammation in the aged brain. Importantly, In vivo, these changes correlate with increased blood-brain barrier permeability and increased anxiety-like behaviour. Of note, the acceleration of senescence-associated markers in the absence of tert occurs not only in the expected proliferative areas but also in non-proliferative ones, where it is unlikely due to telomere-dependent replicative exhaustion, suggesting that non-canonical roles of telomerase may be involved. Together, our work suggests that telomerase has a protective role in the zebrafish brain against the accumulation of senescence and neuro-inflammation and is required for blood-brain barrier integrity. GRAPHICAL ABSTRACT O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=88 SRC="FIGDIR/small/493215v4_ufig1.gif" ALT="Figure 1"> View larger version (20K): org.highwire.dtl.DTLVardef@12d3171org.highwire.dtl.DTLVardef@8f45eorg.highwire.dtl.DTLVardef@1e37580org.highwire.dtl.DTLVardef@372777_HPS_FORMAT_FIGEXP M_FIG Graphical Abstract Telomerase depletion accelerates markers of ageing in the zebrafish brain, ranging from dysregulated immune and stress ageing transcriptomic hallmarks to in situ accumulation of senescence-associated markers and inflammation, dysfunction of the blood-brain barrier and increased anxiety behaviour. C_FIG
- organism: zebrafish
- assay: bulk RNA-seq
- research focus: cell type annotation
- research focus: differential expression
- research focus: cell signaling & trafficking
- research focus: development & morphogenesis
- approach: experimental assay
- Citations
- 5
- FWCI
- 3.19
- Field percentile
- top 8%
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