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Tau Knockout and α-Synuclein A53T Synergy Modulated Parvalbumin-Positive Neurons Degeneration Staging in Substantia Nigra Pars Reticulata of Parkinson’s Disease-Liked Model
The loss of parvalbumin-positive (PV(+)) neurons in the substantia nigra pars reticulata (SNR) was observed in patients with end-stage Parkinson’s disease (PD) and our previously constructed old-aged Pitx3-A53Tα-Syn × Tau(–/–) triple transgenic mice model of PD. The aim of this study was to examine...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8787263/ https://www.ncbi.nlm.nih.gov/pubmed/35087392 http://dx.doi.org/10.3389/fnagi.2021.784665 |
Sumario: | The loss of parvalbumin-positive (PV(+)) neurons in the substantia nigra pars reticulata (SNR) was observed in patients with end-stage Parkinson’s disease (PD) and our previously constructed old-aged Pitx3-A53Tα-Syn × Tau(–/–) triple transgenic mice model of PD. The aim of this study was to examine the progress of PV(+) neurons loss. We demonstrated that, as compared with non-transgenic (nTg) mice, the accumulation of α-synuclein in the SNR of aged Pitx3-A53Tα-Syn × Tau(–/–) mice was increased obviously, which was accompanied by the considerable degeneration of PV(+) neurons and the massive generation of apoptotic NeuN(+)TUNEL(+) co-staining neurons. Interestingly, PV was not costained with TUNEL, a marker of apoptosis. PV(+) neurons in the SNR may undergo a transitional stage from decreased expression of PV to increased expression of NeuN and then to TUNEL expression. In addition, the degeneration of PV(+) neurons and the expression of NeuN were rarely observed in the SNR of nTg and the other triple transgenic mice. Hence, we propose that Tau knockout and α-syn A53T synergy modulate PV(+) neurons degeneration staging in the SNR of aged PD-liked mice model, and NeuN may be suited for an indicator that suggests degeneration of SNR PV(+) neurons. However, the molecular mechanism needs to be further investigated. |
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