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Possible roles of deep cortical neurons and oligodendrocytes in the neural basis of human sociality

Usui, Noriyoshi 大阪大学

2023.11.27

概要

Sociality is a higher order brain function that is essential
for living within a community. Sociality is formed through
relationships with others, and accumulating social experience leads to higher levels of sociality (Kappeler et al. 2015;
Sachser et al. 2013; Tomasello 2020). ...

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参考文献

Abbott NJ, Rönnbäck L, Hansson E (2006) Astrocyte-endothelial interactions at the blood-brain barrier. Nat Rev Neurosci 7:41–53

Agid O, Kohn Y, Lerer B (2000) Environmental stress and psychiatric

illness. Biomed Pharmacother 54:135–141

Alberini CM, Travaglia A (2017) Infantile Amnesia: A Critical Period

of Learning to Learn and Remember. The Journal of Neuroscience : the Official Journal of the Society for Neuroscience

37:5783–5795

Amaral DG, Schumann CM, Nordahl CW (2008) Neuroanatomy of

autism. Trends Neurosci 31:137–145

American Psychiatric Association (2013) Diagnostic and Statistical

Manual of Mental Disorders (DSM-5). Washington, DC

Andrews DS, Lee JK, Harvey DJ et al (2021) A longitudinal study of

white matter development in relation to changes in autism severity across early childhood. Biol Psychiatry 89:424–432

Antunes FM, Malmierca MS (2021) Corticothalamic pathways in auditory processing: recent advances and insights from other sensory

systems. Front Neural Circ 15:721186

Araujo DJ, Anderson AG, Berto S et al (2015) FoxP1 orchestration

of ASD-relevant signaling pathways in the striatum. Genes Dev

29:2081–2096

Possible roles of deep cortical neurons and oligodendrocytes in the neural basis of human…

Araujo DJ, Toriumi K, Escamilla CO et al (2017) Foxp1 in forebrain

pyramidal neurons controls gene expression required for spatial

learning and synaptic plasticity. J Neurosci 37:10917–10931

Bacchelli E, Loi E, Cameli C et al (2019) Analysis of a sardinian multiplex family with autism spectrum disorder points to post-synaptic

density gene variants and identifies CAPG as a functionally relevant candidate gene. J Clin Med 8:212

Bacon C, Rappold GA (2012) The distinct and overlapping phenotypic

spectra of FOXP1 and FOXP2 in cognitive disorders. Hum Genet

131:1687–1698

Bacon C, Schneider M, Le Magueresse C et al (2015) Brain-specific

Foxp1 deletion impairs neuronal development and causes autistic-like behaviour. Mol Psychiatry 20:632–639

Baker A, Kalmbach B, Morishima M, Kim J, Juavinett A, Li N, Dembrow N (2018) Specialized subpopulations of deep-layer pyramidal neurons in the neocortex: bridging cellular properties to functional consequences. J Neurosci 38:5441–5455

Barak B, Feng G (2016) Neurobiology of social behavior abnormalities in autism and Williams syndrome. Nat Neurosci 19:647–655

Barnea-Goraly N, Kwon H, Menon V, Eliez S, Lotspeich L, Reiss AL

(2004) White matter structure in autism: preliminary evidence

from diffusion tensor imaging. Biol Psychiatry 55:323–326

Bedogni F, Hodge RD, Elsen GE et al (2010) Tbr1 regulates regional

and laminar identity of postmitotic neurons in developing neocortex. Proc Natl Acad Sci USA 107:13129–13134

Bertero A, Verrillo L, Apicella AJ (2022) A novel layer 4 corticofugal

cell type/projection involved in thalamo-cortico-striatal sensory

processing. J Neurosci 42:1383–1405

Berto S, Mendizabal I, Usui N et al (2019) Accelerated evolution of

oligodendrocytes in the human brain. Proc Natl Acad Sci USA

116:24334–24342

Butovsky O, Weiner HL (2018) Microglial signatures and their role in

health and disease. Nat Rev Neurosci 19:622–635

Caglayan E, Ayhan F, Liu Y et al (2023) Molecular features driving cellular complexity of human brain evolution. Nature 620:145–153

Cascio CJ, Moore D, Mcglone F (2019) Social touch and human development. Dev Cogn Neurosci 35:5–11

Castelijns B, Baak ML, Timpanaro IS et al (2020) Hominin-specific

regulatory elements selectively emerged in oligodendrocytes and

are disrupted in autism patients. Nat Commun 11:301

Charrier C, Joshi K, Coutinho-Budd J et al (2012) Inhibition of

SRGAP2 function by its human-specific paralogs induces

neoteny during spine maturation. Cell 149:923–935

Co M, Anderson AG, Konopka G (2020a) FOXP transcription factors

in vertebrate brain development, function, and disorders. Wiley

Interdiscip Rev Dev Biol 9:e375

Co M, Hickey SL, Kulkarni A, Harper M, Konopka G (2020b) Cortical Foxp2 supports behavioral flexibility and developmental

dopamine D1 receptor expression. Cereb Cortex 30:1855–1870

Co M, Barnard RA, Jahncke JN et al (2022) Shared and distinct functional effects of patient-specific Tbr1 mutations on cortical development. J Neurosci 42:7166–7181

Consiglio CR, Brodin P (2020) Stressful beginnings with long-term

consequences. Cell 180:820–821

Darmanis S, Sloan SA, Zhang Y et al (2015) A survey of human brain

transcriptome diversity at the single cell level. Proc Natl Acad

Sci USA 112:7285–7290

De Faria Jr. O, Pivonkova H, Varga B, Timmler S, Evans KA, Káradóttir RT (2021) Periods of synchronized myelin changes shape

brain function and plasticity. Nat Neurosci 24:1508–1521

De La Torre-Ubieta L, Won H, Stein JL, Geschwind DH (2016)

Advancing the understanding of autism disease mechanisms

through genetics. Nat Med 22:345–361

Defelipe J (2011) The evolution of the brain, the human nature of cortical circuits, and intellectual creativity. Front Neuroanat 5:29

Demontis D, Walters RK, Martin J et al (2019) Discovery of the first

genome-wide significant risk loci for attention deficit/hyperactivity disorder. Nat Genet 51:63–75

Dennis MY, Nuttle X, Sudmant PH et al (2012) Evolution of humanspecific neural SRGAP2 genes by incomplete segmental duplication. Cell 149:912–922

Doan RN, Shin T, Walsh CA (2018) Evolutionary changes in transcriptional regulation: insights into human behavior and neurological

conditions. Annu Rev Neurosci 41:185–206

Doi M, Li M, Usui N, Shimada S (2022a) Genomic strategies for

understanding the pathophysiology of autism spectrum disorder.

Front Mol Neurosci 15:930941

Doi M, Usui N, Shimada S (2022b) Prenatal environment and neurodevelopmental disorders. Front Endocrinol (lausanne) 13:860110

Donahue CJ, Glasser MF, Preuss TM, Rilling JK, Van Essen DC (2018)

Quantitative assessment of prefrontal cortex in humans relative to

nonhuman primates. Proc Natl Acad Sci USA 115:E5183-e5192

Duan H, Wearne SL, Rocher AB, Macedo A, Morrison JH, Hof PR

(2003) Age-related dendritic and spine changes in corticocortically projecting neurons in macaque monkeys. Cereb Cortex

13:950–961

Dunbar RI, Shultz S (2007) Evolution in the social brain. Science (new

York, N.y.) 317:1344–1347

Elston GN, Benavides-Piccione R, Defelipe J (2001) The pyramidal

cell in cognition: a comparative study in human and monkey. J

Neurosci 21:Rc163

Enard W, Przeworski M, Fisher SE et al (2002) Molecular evolution

of FOXP2, a gene involved in speech and language. Nature

418:869–872

Enard W, Gehre S, Hammerschmidt K et al (2009) A humanized

version of Foxp2 affects cortico-basal ganglia circuits in mice.

Cell 137:961–971

Fan X, Fu Y, Zhou X et al (2020) Single-cell transcriptome analysis

reveals cell lineage specification in temporal-spatial patterns

in human cortical development. Sci Adv 6:eaaz2978

Fazel Darbandi S, Robinson Schwartz SE, Qi Q et al (2018) Neonatal Tbr1 dosage controls cortical layer 6 connectivity. Neuron

100:831-845.e7

Ferguson KT, Cassells RC, Macallister JW, Evans GW (2013) The

physical environment and child development: an international

review. Int J Psychol 48:437–468

Fessel J (2022) Abnormal oligodendrocyte function in schizophrenia explains the long latent interval in some patients. Transl

Psychiatry 12:120

Fiddes IT, Lodewijk GA, Mooring M et al (2018) Human-specific

NOTCH2NL genes affect notch signaling and cortical neurogenesis. Cell 173:1356-1369.e22

Fields RD (2015) A new mechanism of nervous system plasticity:

activity-dependent myelination. Nat Rev Neurosci 16:756–767

Florio M, Albert M, Taverna E et al (2015) Human-specific gene

ARHGAP11B promotes basal progenitor amplification and

neocortex expansion. Science (new York, N.y.) 347:1465–1470

Florio M, Borrell V, Huttner WB (2017) Human-specific genomic

signatures of neocortical expansion. Curr Opin Neurobiol

42:33–44

Fontenot MR, Berto S, Liu Y et al (2017) Novel transcriptional networks regulated by CLOCK in human neurons. Genes Dev

31:2121–2135

Gandal MJ, Zhang P, Hadjimichael E et al (2018) Transcriptome-wide

isoform-level dysregulation in ASD, schizophrenia, and bipolar

disorder. Science 362:eaat8127

Gandhi T, Lee CC (2020) Neural mechanisms underlying repetitive

behaviors in rodent models of autism spectrum disorders. Front

Cell Neurosci 14:592710

Geschwind DH, Konopka G (2012) Neuroscience: genes and human

brain evolution. Nature 486:481–482

13

N. Usui

Gordon A, Geschwind DH (2020) Human in vitro models for understanding mechanisms of autism spectrum disorder. Molecular

Autism 11:26

Griswold AJ, Dueker ND, Van Booven D et al (2015) Targeted massively parallel sequencing of autism spectrum disorder-associated

genes in a case control cohort reveals rare loss-of-function risk

variants. Mol Autism 6:43

Guo W, Clause AR, Barth-Maron A, Polley DB (2017) A corticothalamic circuit for dynamic switching between feature detection

and discrimination. Neuron 95:180-194.e5

Hadjikhani N, Joseph RM, Snyder J, Tager-Flusberg H (2006) Anatomical differences in the mirror neuron system and social cognition

network in autism. Cereb Cortex 16:1276–1282

Hamdan FF, Daoud H, Rochefort D et al (2010) De novo mutations in

FOXP1 in cases with intellectual disability, autism, and language

impairment. Am J Hum Genet 87:671–678

Han X, Chen M, Wang F et al (2013) Forebrain engraftment by human

glial progenitor cells enhances synaptic plasticity and learning in

adult mice. Cell Stem Cell 12:342–353

Harris KD, Shepherd GM (2015) The neocortical circuit: themes and

variations. Nat Neurosci 18:170–181

Heide M, Haffner C, Murayama A et al (2020) Human-specific ARHGAP11B increases size and folding of primate neocortex in the

fetal marmoset. Science (new York, N.y.) 369:546–550

Heim CP, Meinlschmidt GMS, Nemeroff CBMDP (2003) Neurobiology of early-life stress. Psychiatr Ann 33:18–26

Heim C, Plotsky PM, Nemeroff CB (2004) Importance of studying the contributions of early adverse experience to neurobiological findings in depression. Neuropsychopharmacology

29:641–648

Herculano-Houzel S (2009) The human brain in numbers: a linearly

scaled-up primate brain. Front Hum Neurosci 3:31

Herculano-Houzel S (2012) The remarkable, yet not extraordinary,

human brain as a scaled-up primate brain and its associated

cost. Proc Natl Acad Sci USA 109(Suppl 1):10661–10668

Hirai T, Usui N, Iwata K et al (2020) Increased plasma lipoprotein

lipase activity in males with autism spectrum disorder. Res

Autism Spectrum Disord 77:101630

Huang TN, Chuang HC, Chou WH, Chen CY, Wang HF, Chou SJ,

Hsueh YP (2014) Tbr1 haploinsufficiency impairs amygdalar

axonal projections and results in cognitive abnormality. Nat

Neurosci 17:240–247

Huang W, Bhaduri A, Velmeshev D et al (2020) Origins and proliferative states of human oligodendrocyte precursor cells. Cell

182:594-608.e11

Inoue N, Nishizumi H, Ooyama R, Mogi K, Nishimori K, Kikusui

T, Sakano H (2021) The olfactory critical period is determined

by activity-dependent Sema7A/PlxnC1 signaling within glomeruli. eLife 10:e65078

Iossifov I, O’Roak BJ, Sanders SJ et al (2014) The contribution of

de novo coding mutations to autism spectrum disorder. Nature

515:216–221

Irie K, Doi M, Usui N, Shimada S (2022) Evolution of the human

brain can help determine pathophysiology of neurodevelopmental disorders. Front Neurosci 16:871979

Jethava V, Kadish J, Kakonge L, Wiseman-Hakes C (2022) Early

attachment and the development of social communication: a

neuropsychological approach. Front Psych 13:838950

Kappeler PM, Cremer S, Nunn CL (2015) Sociality and health:

impacts of sociality on disease susceptibility and transmission in animal and human societies. Philos Trans R Soc Lond

B Biol Sci 370:20140116

Kast RJ, Lanjewar AL, Smith CD, Levitt P (2019) FOXP2 exhibits

projection neuron class specific expression, but is not required

for multiple aspects of cortical histogenesis. eLife 8:e42012

13

Kawamura A, Katayama Y, Nishiyama M et al (2020) Oligodendrocyte dysfunction due to Chd8 mutation gives rise to behavioral

deficits in mice. Hum Mol Genet 29:1274–1291

Khodosevich K, Sellgren CM (2023) Neurodevelopmental disordershigh-resolution rethinking of disease modeling. Mol Psychiatry

28:34–43

Kim J, Matney CJ, Blankenship A, Hestrin S, Brown SP (2014)

Layer 6 corticothalamic neurons activate a cortical output

layer, layer 5a. J Neurosci 34:9656–9664

Kokkosis AG, Madeira MM, Mullahy MR, Tsirka SE (2022) Chronic

stress disrupts the homeostasis and progeny progression of oligodendroglial lineage cells, associating immune oligodendrocytes with prefrontal cortex hypomyelination. Mol Psychiatry

27:2833–2848

Konopka G, Bomar JM, Winden K et al (2009) Human-specific transcriptional regulation of CNS development genes by FOXP2.

Nature 462:213–217

Konopka G, Friedrich T, Davis-Turak J et al (2012) Human-specific

transcriptional networks in the brain. Neuron 75:601–617

Lai CS, Fisher SE, Hurst JA, Vargha-Khadem F, Monaco AP (2001)

A forkhead-domain gene is mutated in a severe speech and

language disorder. Nature 413:519–523

Landers MS, Sullivan RM (2012) The development and neurobiology of infant attachment and fear. Dev Neurosci 34:101–114

Li Q, Barres BA (2018) Microglia and macrophages in brain homeostasis and disease. Nat Rev Immunol 18:225–242

Li M, Usui N, Shimada S (2023) Prenatal sex hormone exposure is

associated with the development of autism spectrum disorder.

Int J Mol Sci 24:2203

Liu J, Liu W, Yang L et al (2017) The primate-specific gene TMEM14B

marks outer radial glia cells and promotes cortical expansion and

folding. Cell Stem Cell 21:635-649.e8

Loomba S, Straehle J, Gangadharan V et al (2022) Connectomic comparison of mouse and human cortex. Science (new York, N.y.)

377:eabo0924

Lord C, Elsabbagh M, Baird G, Veenstra-Vanderweele J (2018) Autism

spectrum disorder. Lancet 392:508–520

Lord C, Ts B, Charman T et al (2020) Autism spectrum disorder. Nat

Rev Dis Primers 6:5

Lozano R, Vino A, Lozano C, Fisher SE, Deriziotis P (2015) A de novo

FOXP1 variant in a patient with autism, intellectual disability

and severe speech and language impairment. Eur J Human Genet

23:1702–1707

Mackes NK, Golm D, Sarkar S et al (2020) Early childhood deprivation is associated with alterations in adult brain structure despite

subsequent environmental enrichment. Proc Natl Acad Sci USA

117:641–649

Makinodan M, Rosen KM, Ito S, Corfas G (2012) A critical period

for social experience-dependent oligodendrocyte maturation and

myelination. Science (new York, N.y.) 337:1357–1360

Mendizabal I, Berto S, Usui N et al (2019) Cell type-specific epigenetic

links to schizophrenia risk in the brain. Genome Biol 20:135

Miguel PM, Pereira LO, Silveira PP, Meaney MJ (2019) Early environmental influences on the development of children’s brain

structure and function. Dev Med Child Neurol 61:1127–1133

Miller DJ, Duka T, Stimpson CD et al (2012) Prolonged myelination in human neocortical evolution. Proc Natl Acad Sci USA

109:16480–16485

Miyata S, Hattori T, Shimizu S, Ito A, Tohyama M (2015) Disturbance

of oligodendrocyte function plays a key role in the pathogenesis

of schizophrenia and major depressive disorder. Biomed Res Int

2015:492367

Mohan H, An X, Xu XH et al (2023) Cortical glutamatergic projection

neuron types contribute to distinct functional subnetworks. Nat

Neurosci 26:481–494

Possible roles of deep cortical neurons and oligodendrocytes in the neural basis of human…

Nagy C, Maitra M, Tanti A et al (2020) Single-nucleus transcriptomics

of the prefrontal cortex in major depressive disorder implicates

oligodendrocyte precursor cells and excitatory neurons. Nat Neurosci 23:771–781

Namba T, Dóczi J, Pinson A et al (2020) Human-specific ARHGAP11B acts in mitochondria to expand neocortical progenitors

by glutaminolysis. Neuron 105:867-881.e9

Nambot S, Faivre L, Mirzaa G et al (2020) De novo TBR1 variants

cause a neurocognitive phenotype with ID and autistic traits:

report of 25 new individuals and review of the literature. Eur J

Human Genet EJHG 28:770–782

Notwell JH, Heavner WE, Darbandi SF et al (2016) TBR1 regulates

autism risk genes in the developing neocortex. Genome Res

26:1013–1022

O’Roak BJ, Deriziotis P, Lee C et al (2011) Exome sequencing in

sporadic autism spectrum disorders identifies severe de novo

mutations. Nat Genet 43:585–589

Pattabiraman K, Muchnik SK, Sestan N (2020) The evolution of the

human brain and disease susceptibility. Curr Opin Genet Dev

65:91–97

Phan BN, Bohlen JF, Davis BA et al (2020) A myelin-related transcriptomic profile is shared by Pitt-Hopkins syndrome models

and human autism spectrum disorder. Nat Neurosci 23:375–385

Polioudakis D, De La Torre-Ubieta L, Langerman J et al (2019) A

Single-cell transcriptomic atlas of human neocortical development during mid-gestation. Neuron 103:785-801.e8

Quesnel-Vallières M, Weatheritt RJ, Cordes SP, Blencowe BJ (2019)

Autism spectrum disorder: insights into convergent mechanisms

from transcriptomics. Nat Rev Genet 20:51–63

Reh RK, Dias BG, Nelson III CA et al (2020) Critical period regulation across multiple timescales. Proc Natl Acad Sci USA

117:23242–23251

Reuter MS, Riess A, Moog U et al (2017) FOXP2 variants in 14

individuals with developmental speech and language disorders

broaden the mutational and clinical spectrum. J Med Genet

54:64–72

Richardson WD, Kessaris N, Pringle N (2006) Oligodendrocyte wars.

Nat Rev Neurosci 7:11–18

Rilling JK, Van Den Heuvel MP (2018) Comparative primate connectomics. Brain Behav Evol 91:170–179

Rivers LE, Young KM, Rizzi M et al (2008) PDGFRA/NG2 glia generate myelinating oligodendrocytes and piriform projection neurons in adult mice. Nat Neurosci 11:1392–1401

Roth TL, Raineki C, Salstein L et al (2013) Neurobiology of secure

infant attachment and attachment despite adversity: a mouse

model. Genes Brain Behav 12:673–680

Russo SJ, Nestler EJ (2013) The brain reward circuitry in mood disorders. Nat Rev Neurosci 14:609–625

Sachser N, Kaiser S, Hennessy MB (2013) Behavioural profiles are

shaped by social experience: when, how and why. Philos Trans

R Soc Lond B Biol Sci 368:20120344

Sakano H (2020) Developmental regulation of olfactory circuit formation in mice. Dev Growth Differ 62:199–213

Sanders SJ, He X, Willsey AJ et al (2015) Insights into autism spectrum disorder genomic architecture and biology from 71 risk loci.

Neuron 87:1215–1233

Sapey-Triomphe LA, Reversat J, Lesca G et al (2020) A de novo

frameshift pathogenic variant in TBR1 identified in autism without intellectual disability. Hum Genom 14:32

Satterstrom FK, Kosmicki JA, Wang J et al (2020) Large-scale exome

sequencing study implicates both developmental and functional

changes in the neurobiology of autism. Cell 180:568-584.e23

Šeda O, Šedová L, Včelák J, Vaňková M, Liška F, Bendlová B (2017)

ZBTB16 and metabolic syndrome: a network perspective. Physiol Res 66:S357-s365

Sherwood CC, Stimpson CD, Raghanti MA et al (2006) Evolution of

increased glia-neuron ratios in the human frontal cortex. Proc

Natl Acad Sci USA 103:13606–13611

Shibata M, Pattabiraman K, Muchnik SK et al (2021) Hominini-specific regulation of CBLN2 increases prefrontal spinogenesis.

Nature 598:489–494

Shin Yim Y, Park A, Berrios J et al (2017) Reversing behavioural

abnormalities in mice exposed to maternal inflammation. Nature

549:482–487

Silk JB (2007) Social components of fitness in primate groups. Science

(new York, N.y.) 317:1347–1351

Siper PM, De Rubeis S, Trelles MDP et al (2017) Prospective investigation of FOXP1 syndrome. Molecular Autism 8:57

Sonuga-Barke EJS, Kennedy M, Kumsta R et al (2017) Child-to-adult

neurodevelopmental and mental health trajectories after early

life deprivation: the young adult follow-up of the longitudinal

English and Romanian Adoptees study. Lancet 389:1539–1548

Sorensen SA, Bernard A, Menon V et al (2015) Correlated gene

expression and target specificity demonstrate excitatory projection neuron diversity. Cereb Cortex 25:433–449

Stessman HA, Xiong B, Coe BP et al (2017) Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and

developmental-disability biases. Nat Genet 49:515–526

Stoner R, Chow ML, Boyle MP et al (2014) Patches of disorganization in the neocortex of children with autism. N Engl J Med

370:1209–1219

Suliman BA, Xu D, WIlliams BR (2012) The promyelocytic leukemia

zinc finger protein: two decades of molecular oncology. Front

Oncol 2:74

Suzuki IK, Gacquer D, Van Heurck R et al (2018) Human-Specific

NOTCH2NL genes expand cortical neurogenesis through delta/

notch regulation. Cell 173:1370-1384.e16

Takesian AE, Hensch TK (2013) Balancing plasticity/stability across

brain development. Prog Brain Res 207:3–34

Tasic B, Menon V, Nguyen TN et al (2016) Adult mouse cortical cell

taxonomy revealed by single cell transcriptomics. Nat Neurosci

19:335–346

Tebbenkamp AT, Willsey AJ, State MW, Sestan N (2014) The developmental transcriptome of the human brain: implications for

neurodevelopmental disorders. Curr Opin Neurol 27:149–156

Teicher MH, Samson JA, Anderson CM, Ohashi K (2016) The effects

of childhood maltreatment on brain structure, function and connectivity. Nat Rev Neurosci 17:652–666

Teissier A, Le Magueresse C, Olusakin J et al (2020) Early-life stress

impairs postnatal oligodendrogenesis and adult emotional behaviour through activity-dependent mechanisms. Mol Psychiatry

25:1159–1174

Thompson A, Shahidiani A, Fritz A et al (2020) Age-related differences in white matter diffusion measures in autism spectrum

condition. Molecular Autism 11:36

Thomson AM (2010) Neocortical layer 6, a review. Front Neuroanat

4:13

Toma C, Torrico B, Hervás A et al (2014) Exome sequencing in multiplex autism families suggests a major role for heterozygous

truncating mutations. Mol Psychiatry 19:784–790

Tomasello M (2020) The adaptive origins of uniquely human sociality.

Philos Trans R Soc Lond B Biol Sci 375:20190493

Trutzer IM, García-Cabezas M, Zikopoulos B (2019) Postnatal development and maturation of layer 1 in the lateral prefrontal cortex

and its disruption in autism. Acta Neuropathol Commun 7:40

Usui N, Co M, Konopka G (2014) Decoding the molecular evolution

of human cognition using comparative genomics. Brain Behav

Evol 84:103–116

13

N. Usui

Usui N, Araujo DJ, Kulkarni A et al (2017a) Foxp1 regulation of

neonatal vocalizations via cortical development. Genes Dev

31:2039–2055

Usui N, Co M, Harper M, Rieger MA, Dougherty JD, Konopka G

(2017b) Sumoylation of FOXP2 regulates motor function and

vocal communication through purkinje cell development. Biol

Psychiatry 81:220–230

Usui N, Iwata K, Miyachi T et al (2020) VLDL-specific increases of

fatty acids in autism spectrum disorder correlate with social

interaction. EBioMedicine 58:102917

Usui N, Berto S, Konishi A, Kondo M, Konopka G, Matsuzaki H,

Shimada S (2021a) Zbtb16 regulates social cognitive behaviors

and neocortical development. Transl Psychiatry 11:242

Usui N, Ono Y, Aramaki R, Berto S, Konopka G, Matsuzaki H, Shimada S (2021b) Early life stress alters gene expression and cytoarchitecture in the prefrontal cortex leading to social impairment

and increased anxiety. Front Genet 12:754198

Usui N, Matsumoto-Miyai K, Koyama Y, Kobayashi Y, Nakamura

Y, Kobayashi H, Shimada S (2022a) Social communication of

maternal immune activation-affected offspring is improved by

si-based hydrogen-producing agent. Front Psych 13:872302

Usui N, Tian X, Harigai W et al (2022b) Length impairments of the

axon initial segment in rodent models of attention-deficit hyperactivity disorder and autism spectrum disorder. Neurochem Int

153:105273

Usui N, Kobayashi H, Shimada S (2023) Neuroinflammation and oxidative stress in the pathogenesis of autism spectrum disorder. Int

J Mol Sci 24:5487

Van Heurck R, Bonnefont J, Wojno M et al (2023) CROCCP2 acts as a

human-specific modifier of cilia dynamics and mTOR signaling

to promote expansion of cortical progenitors. Neuron 111:6580.e6

Vanderhaeghen P, Polleux F (2023) Developmental mechanisms underlying the evolution of human cortical circuits. Nat Rev Neurosci

24:213–232

Vegas N, Cavallin M, Kleefstra T et al (2018) Mutations in TBR1 gene

leads to cortical malformations and intellectual disability. Eur J

Med Genet 61:759–764

Vivanti G, Nuske HJ (2017) Autism, attachment, and social learning: Three challenges and a way forward. Behav Brain Res

325:251–259

13

Volterra A, Meldolesi J (2005) Astrocytes, from brain glue to communication elements: the revolution continues. Nat Rev Neurosci

6:626–640

Von Bartheld CS, Bahney J, Herculano-Houzel S (2016) The search

for true numbers of neurons and glial cells in the human

brain: a review of 150 years of cell counting. J Comp Neurol

524:3865–3895

Wang SS, Kloth AD, Badura A (2014) The cerebellum, sensitive periods, and autism. Neuron 83:518–532

Wang T, Hoekzema K, Vecchio D et al (2020) Large-scale targeted

sequencing identifies risk genes for neurodevelopmental disorders. Nat Commun 11:4932

Wilkinson B, Grepo N, Thompson BL et al (2015) The autism-associated gene chromodomain helicase DNA-binding protein 8

(CHD8) regulates noncoding RNAs and autism-related genes.

Transl Psychiatry 5:e568

Willsey AJ, Sanders SJ, Li M et al (2013) Coexpression networks

implicate human midfetal deep cortical projection neurons in

the pathogenesis of autism. Cell 155:997–1007

Willsey HR, Willsey AJ, Wang B, State MW (2022) Genomics, convergent neuroscience and progress in understanding autism spectrum disorder. Nat Rev Neurosci 23:323–341

Yao P, Lin P, Gokoolparsadh A, Assareh A, Thang MW, Voineagu

I (2015) Coexpression networks identify brain region-specific

enhancer RNAs in the human brain. Nat Neurosci 18:1168–1174

Ms Y, Zdunek S, Bergmann O et al (2014) Dynamics of oligodendrocyte generation and myelination in the human brain. Cell

159:766–774

Zhao S, Hu X, Park J et al (2007) Selective expression of LDLR

and VLDLR in myelinating oligodendrocytes. Dev Dyn

236:2708–2712

Zhou B, Zhu Z, Ransom BR, Tong X (2021) Oligodendrocyte lineage

cells and depression. Mol Psychiatry 26:103–117

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