Progressive tau aggregation does not alter functional brain network connectivity in seeded hTau.P301L mice
Author(s) -
Jan R. Detrez,
Inès R. H. Ben-Nejma,
Kristof Van Kolen,
Debby Van Dam,
Peter Paul De Deyn,
Erik Fransén,
Marleen Verhoye,
JeanPierre Timmermans,
Rony Nuydens,
Annemie Van der Linden,
Georgios A. Keliris,
Winnok H. De Vos
Publication year - 2020
Publication title -
neurobiology of disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.205
H-Index - 166
eISSN - 1095-953X
pISSN - 0969-9961
DOI - 10.1016/j.nbd.2020.105011
Subject(s) - tau pathology , neuroscience , tauopathy , functional connectivity , biology , resting state fmri , tau protein , alzheimer's disease , pathology , disease , medicine , neurodegeneration
Progressive accumulation of hyperphosphorylated tau is a hallmark of various neurodegenerative disorders including Alzheimer's disease. However, to date, the functional effects of tau pathology on brain network connectivity have been investigated to a limited extent. To directly interrogate the impact of tau pathology on functional brain connectivity, we conducted a longitudinal experiment in which we monitored a seeded hTau.P301L mouse model using correlative whole-brain microscopy and resting-state functional MRI. Despite a progressive aggravation of tau pathology across the brain, the major resting-state networks appeared unaffected up to 15 weeks after seeding. Targeted analyses also showed that the connectivity of regions with high levels of hyperphosphorylated tau was comparable to that observed in controls. In line with the ostensible retention of connectivity, no behavioural changes were detected between seeded and control mice as determined by three different paradigms. Our data indicate that seeded tau pathology, with accumulation of tau aggregates throughout different regions of the brain, does not alter functional connectivity or behaviour in this model. Additional correlative functional studies on different mouse models should help determine whether this is a generalizable trait of tauopathies.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom