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Transcriptomic taxonomy and neurogenic trajectories of adult human, macaque, and pig hippocampal and entorhinal cells
Open accessAbstract
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 humans, macaques, and pigs. Integrated cross-species analysis revealed robust transcriptomic and histologic signatures of neurogenesis in the 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. This resource reveals cell-type- and species-specific properties shaping hippocampal-entorhinal neurogenesis and function.
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“EC-specific subtypes that clustered separately from neocortical subtypes for the same layers were often marked by expression of RELN, TOX3 and GPC5, and contained subtypes from both the lateral (L2 RELN+GPC5+) and medial (L2 TOX3+POSTN+) EC41–43”
From Single-cell multiregion dissection of Alzheimer’s disease (2024) · cites this paper as [41]
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“Five of the miR-132 targets (BMI1, FOXO1, SPRY1, DPYSL3, CITED2) displaying the highest betweenness centrality, a proxy of network connectivity, have all shown to be involved in cell cycle, and more specifically, in neurogenesis [68–72] (Fig. 5D) (Supplementary Table 7).”
From microRNA-132 attenuates inflammation in induced pluripotent stem cell-derived microglia from Alzheimer’s disease patients (2026) · cites this paper as [70]
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“Although some brain regions relevant to AD have been studied individually at scale or jointly in samples from a few individuals8–16, a comprehensive molecular characterization of region-specific differences in AD is currently lacking”
From Single-cell multiregion dissection of Alzheimer’s disease (2024) · cites this paper as [13]
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“Five of the miR-132 targets (BMI1, FOXO1, SPRY1, DPYSL3, CITED2) displaying the highest betweenness centrality, a proxy of network connectivity, have all shown to be involved in cell cycle, and more specifically, in neurogenesis [68–72] (Fig. 5D) (Supplementary Table 7).”
From microRNA-132 attenuates inflammation in induced pluripotent stem cell-derived microglia from Alzheimer’s disease patients (2026) · cites this paper as [70]
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“Our data indicate that while there are common ‘core’ miR-132 targets across conditions, possibly involved in ‘housekeeping’ cellular functions, like cell cycle [68–72], there are also context-dependent targets, specific to healthy control or sAD iMGs.”
From microRNA-132 attenuates inflammation in induced pluripotent stem cell-derived microglia from Alzheimer’s disease patients (2026) · cites this paper as [70]
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“Some groups have reported absent or minimal hippocampal neurogenesis in the mature brain using double immunofluorescence targeting markers expressed by neuronal cells at different maturational stages95, 96 and single nucleus transcriptomics97.”
From Dysregulation of adult hippocampal neuroplasticity in major depression: Pathogenesis and therapeutic implications (2022) · cites this paper as [97]
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“The explanatory power of neurogenesis in depression and antidepressant drug effects is complicated by the fact that neurogenesis is only observed in the dentate gyrus, putting a severe limit on the possible depression symptom domains it can impact, and by recent findings that neurogenesis may be very limited or absent in humans [102].”
From Plasticity of synapses and reward circuit function in the genesis and treatment of depression (2023) · cites this paper as [102]
In the citing paper
“We also conducted integration of our ATAC data and scATAC-seq data from human brain samples42 (Fig. 5b), and our RNA data with adult human brain snRNA-seq data43, to show the dominant cell identities and states.”
From Spatial epigenome–transcriptome co-profiling of mammalian tissues (2023) · cites this paper as [43]
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Metadata
- Authors
- Franjic, D., Skarica, M., Ma, S., Arellano, J. I., Tebbenkamp, A. T. N., Choi, J., Xu, C., Li, Q., Morozov, Y. M., 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, S. M., Sousa, A. M. M., Rakic, P., & Sestan, N.
- Affiliations
- Yale University (US)
- Universitat Pompeu Fabra (ES)
- Yale Cancer Center (US)
- ORCID
- Franjic, Daniel
- Ma, Shaojie
- Arellano, Jon I.
- Tebbenkamp, Andrew T.N.
- Choi, Jinmyung
- Xu, Chuan
- Li, Qian
- Morozov, Yury M.
- Andrijevic, David
- Spajic, Ana
- Santpere, Gabriel
- Li, Mingfeng
- Liu, Yang
- Spurrier, Joshua
- Zhang, Le
- Gudelj, Ivan
- Rapan, Lucija
- Takahashi, Hideyuki
- Huttner, Anita
- Fan, Rong
- Strittmatter, Stephen M.
- Rakic, Pasko
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2022-02
- Volume
- 110
- Issue
- 3
- Pages
- 452-469.e14
- ISSN
- 0896-6273 (ISSN-L)
- PMC
- PMC8813897
- OpenAlex
- W3212895337
- Cited by
- 308
- References
- 130
- Citations by year
- 2026: 48 · 2025: 68 · 2024: 58 · 2023: 74 · 2022: 58
- FWCI
- 17.49
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Neuron (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Repositori digital de la UPF (Universitat Pompeu Fabra) (submittedVersion, cc-by-nc-nd)
- Funders
- “la Caixa” Foundation (100010434)
- Instituto de Salud Carlos III (MS20/00064)
- European Social Fund
- Agencia Estatal de Investigación (PID2019-104700GA-I00)
- Fundacion La Caixa
- National Institutes of Health (MH103339, MH106934, MH109904, MH110926)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Single-cell and spatial transcriptomics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- adult neurogenesis, single-nucleus transcriptomics, cross-species comparison, doublecortin, METTL7B, excitatory neurons, astrocytes, lipid droplets, endoplasmic reticulum, granule cells
- MeSH terms
- Doublecortin Protein, Animals, Hippocampus, Humans, Macaca, Swine, Mice, Neurogenesis, Transcriptome
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
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