Transcriptomic taxonomy and neurogenic trajectories of adult human, macaque, and pig hippocampal and entorhinal cells.
Transcriptomic taxonomy and neurogenic trajectories of adult human, macaque, and pig hippocampal and entorhinal cells.
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DOI:
10.1016/j.neuron.2021.10.036
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发表时间:
2022-02-02
期刊:
影响因子:
16.2
通讯作者:
Sestan N
中科院分区:
文献类型:
--
作者:
Franjic D;Skarica M;Ma S;Arellano JI;Tebbenkamp ATN;Choi J;Xu C;Li Q;Morozov YM;Andrijevic D;Vrselja Z;Spajic A;Santpere G;Li M;Zhang S;Liu Y;Spurrier J;Zhang L;Gudelj I;Rapan L;Takahashi H;Huttner A;Fan R;Strittmatter SM;Sousa AMM;Rakic P;Sestan N
The hippocampal-entorhinal system supports cognitive functions, has lifelong neurogenic capabilities in many species, and is selectively vulnerable to Alzheimer’s disease. To investigate neurogenic potential and cellular diversity, we profiled single-nucleus transcriptomes in five hippocampal-entorhinal subregions in human, macaque, and pig. Integrated cross-species analysis revealed robust transcriptomic and histologic signatures of neurogenesis in adult mouse, pig and macaque, but not humans. Doublecortin (DCX), a widely accepted marker of newly generated granule cells, was detected in diverse human neurons, but it did not define immature neuron populations. To explore species differences in cellular diversity and implications for disease, we characterized subregion-specific transcriptomically-defined cell types and transitional changes from the three-layered archicortex to the six-layered neocortex. Notably, METTL7B defined subregion-specific excitatory neurons and astrocytes in primates, associated with endoplasmic reticulum and lipid droplet proteins, including Alzheimer’s disease-related proteins. Together this resource reveals cell-type- and species-specific properties shaping hippocampal-entorhinal neurogenesis and function. Using snRNA-seq of the adult human, macaque and pig hippocampal-entorhinal system, Franjic et al. defined shared and divergent cell type features, like primate-specific expression of METTL7B in some excitatory neurons and astrocytes. They also identified robust transcriptomic and histologic signatures of neurogenesis in mouse, pig and macaque, but not human.
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影响因子:
46.9
作者:
Becht, Etienne;McInnes, Leland;Newell, Evan W.
通讯作者:
Newell, Evan W.
影响因子:
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作者:
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作者:
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5
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通讯作者:
Sutherland GT
DOI:
10.1073/pnas.0804558105
发表时间:
2008-09-02
影响因子:
11.1
作者:
Breunig, Joshua J.;Sarkisian, Matthew R.;Town, Terrence
通讯作者:
Town, Terrence