Animal models of autism: a perspective from autophagy mechanisms

Halime Dana , Reyhan Tahtasakal , Elif Funda Sener

Journal of Translational Genetics and Genomics ›› 2020, Vol. 4 ›› Issue (3) : 251 -262.

PDF
Journal of Translational Genetics and Genomics ›› 2020, Vol. 4 ›› Issue (3) :251 -262. DOI: 10.20517/jtgg.2020.25
Review
review-article

Animal models of autism: a perspective from autophagy mechanisms

Author information +
History +
PDF

Abstract

Autism spectrum disorder (ASD) is characterized by impairments in social interaction and the presence of stereotypy and restrictive behavior. The clinical heterogeneity of ASD makes it difficult to explain the mechanisms underlying the disease. In recent years, the association between autophagy and neuropsychiatric diseases has been investigated. In this review, we aimed elucidate the relationship between autism and autophagy mechanism in well-known autism relevant animal models. Autophagy is a cell-protective mechanism that allows cell survival in low nutrient conditions, often through the degradation of aging and damaged proteins and organelles. The target of rapamycin (TOR) complex is activated for the activation of autophagy. Apart from mTOR animal models, the valproic acid model is frequently used in autism studies. The coiled-coil and C2 domain containing 1A (CC2D1A) gene is one of the new candidate genes associated with ASD. In a recent study that used Cc2d1a knock-out mice, microtubule-associated protein 1A/1B-light chain 3 (LC3) and Beclin 1 expression levels were dysregulated in the hippocampus. It is thought that the impaired autophagy mechanism contributes to the etiology of ASD. These results showed that CC2D1A acts as a new biological pathway in autophagy. Choosing the right model is crucial for ASD studies, and further progress will be made as these results become available in the clinic. In particular, it is expected that further studies on CC2D1A will provide new information in this field.

Keywords

Autism / animal models / autophagy / CC2D1A / mammalian target of rapamycin / valproic acid

Cite this article

Download citation ▾
Halime Dana, Reyhan Tahtasakal, Elif Funda Sener. Animal models of autism: a perspective from autophagy mechanisms. Journal of Translational Genetics and Genomics, 2020, 4(3): 251-262 DOI:10.20517/jtgg.2020.25

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

KumarS,JiY,RaiS.Impaired neurodevelopmental pathways in autism spectrum disorder: a review of signaling mechanisms and crosstalk..J NeurodevDisord2019;11:10 PMCID:PMC6571119

[2]

Woodbury-SmithM.Progress in the genetics of autism spectrum disorder..Dev Med Child Neurol2018;60:445-51

[3]

AnagnostouE,SzatmariP,FernandezBA.Autism spectrum disorder: advances in evidence-based practice..CMAJ2014;186:509-19 PMCID:PMC3986314

[4]

SenerEF,BayramovKK,OztopDB.The roles of CC2D1A and HTR1A gene expressions in autism spectrum disorders..Metab Brain Dis2016;31:613-9

[5]

BölteS,MarschikPB.The contribution of environmental exposure to the etiology of autism spectrum disorder..Cell Mol Life Sci2019;76:1275-97 PMCID:PMC6420889

[6]

BourgeronT.Current knowledge on the genetics of autism and propositions for future research..C R Biol2016;339:300-7

[7]

BangerterA,ManyakovNV,LewinD.Relationship between sleep and behavior in autism spectrum disorder: exploring the impact of sleep variability..Front Neurosci2020;14:211 PMCID:PMC7105870

[8]

PaganC,DelormeR,LemièreN.Disruption of melatonin synthesis is associated with impaired 14-3-3 and miR-451 levels in patients with autism spectrum disorders..Sci Rep2017;7:2096 PMCID:PMC5437096

[9]

RylaarsdamL.Genetic causes and modifiers of autism spectrum disorder..Front Cell Neurosci2019;13:385 PMCID:PMC6710438

[10]

WerlingDM.Sex differences in autism spectrum disorders..Curr Opin Neurol2013;26:146-53 PMCID:PMC4164392

[11]

Nolen-HoeksemaS.The emergence of gender differences in depression during adolescence..Psychol Bull1994;115:424-43

[12]

RynkiewiczA.Autism spectrum disorder (ASD) in girls. Co-occurring psychopathology. Sex differences in clinical manifestation..Psychiat Pol2018;52:629-39

[13]

MossaA.Molecular causes of sex-specific deficits in rodent models of neurodevelopmental disorders..J Neurosci Res2019;

[14]

CarmassiC,CarusoD,NobiliL.Systematic review of sleep disturbances and circadian sleep desynchronization in autism spectrum disorder: toward an integrative model of a self-reinforcing loop..Front Psychiatry2019;10:366 PMCID:PMC6581070

[15]

SenerEF,OzkulY.Recent advances in autism spectrum disorders: applications of whole exome sequencing technology..Psychiatry Investig2016;13:255-64 PMCID:PMC4878959

[16]

ZhangXC,ZhaoXS.Autism spectrum disorders: autistic phenotypes and complicated mechanisms..World J Pediatr2019;15:17-25

[17]

BernardPaulais MA,ThiébautE,Costa Coelho De SouzaMT.Heterogeneities in cognitive and socio-emotional development in children with autism spectrum disorder and severe intellectual disability as a comorbidity..Front Psychiatry2019;10:508 PMCID:PMC6662559

[18]

SenerEF,SahinMC,MarasliMK.Altered global mRNA expressions of pain and aggression related genes in the blood of children with autism spectrum disorders..J of Molecular Neuroscience2019;67:89-96

[19]

RicciardiS,GrossoS,ForlaniG.Reduced AKT/mTOR signaling and protein synthesis dysregulation in a Rett syndrome animal model..Hum Mol Genet2011;20:1182-96

[20]

SciaraAN,CrawfordJD,CarrascoT.Neuroinflammatory gene expression alterations in anterior cingulate cortical white and gray matter of males with autism spectrum disorder..Autism Res2020;13:870-84

[21]

C YuenRK,BookmanM,ThiruvahindrapuramB.Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder..Nat Neurosci2017;20:602-11 PMCID:PMC5501701

[22]

GlessnerJT,CaiG,KimCE.Autism genome-wide copy number variation reveals ubiquitin and neuronal genes..Nature2009;459:569-73 PMCID:PMC2925224

[23]

BaileyA,GottesmanI,SimonoffE.Autism as a strongly genetic disorder: evidence from a British twin study..Psychol Med1995;25:63-77

[24]

NicoliniC.The valproic acid-induced rodent model of autism..Exp Neurol2018;299:217-27

[25]

YinJ.Autism genetics - an overview..Prenat Diagn2017;37:14-30

[26]

BaumanM.Histoanatomic observations of the brain in early infantile autism..Neurology1985;35:866-74

[27]

GuerinP,BarthelemyC,ChevrollierV.Neuropathological study of a case of autistic syndrome with severe mental retardation..Dev Med Child Neurol1996;38:203-11

[28]

HutslerJJ,ZhangH.Histological and magnetic resonance imaging assessment of cortical layering and thickness in autism spectrum disorders..Biol Psychiatry2007;61:449-57

[29]

HutslerJJ.Increased dendritic spine densities on cortical projection neurons in autism spectrum disorders..Brain Res2010;1309:83-94

[30]

BakosJ,GrantSG,OstatnikovaD.Are molecules involved in neuritogenesis and axon guidance related to autism pathogenesis?.Neuromolecular Med2015;17:297-304

[31]

SiniscalcoD,CirilloA.Autism spectrum disorders: is mesenchymal stem cell personalized therapy the future?.J Biomed Biotechnol2012;2012:480289 PMCID:PMC3303614

[32]

SchusterS,StraussU.NOMA-GAP/ARHGAP33 regulates synapse development and autistic-like behavior in the mouse..Mol Psychiatry2015;20:1120-31

[33]

LevittJG,SmalleyS.Cortical sulcal maps in autism..Cereb Cortex Jul2003;13:728-35

[34]

ScottJA,Goodlin-JonesBL.A comprehensive volumetric analysis of the cerebellum in children and adolescents with autism spectrum disorder..Autism Res2009;2:246-57 PMCID:PMC2999464

[35]

MarinoG,BaehreckeEH.Self-consumption: the interplay of autophagy and apoptosis..Nat Rev Mol Cell Biol2014;15:81-94 PMCID:PMC3970201

[36]

CostaL,TeixeiraN,FonsecaBM.Cannabinoid-induced autophagy: protective or death role?.Prostaglandins Other Lipid Mediat2016;122:54-63

[37]

SuZ,XuY,YuQ.Apoptosis, autophagy, necroptosis, and cancer metastasis..Molecular Cancer2015;14:48 PMCID:PMC4343053

[38]

KangR,LotzeMT.The Beclin 1 network regulates autophagy and apoptosis..Cell Death Differ2011;18:571-80 PMCID:PMC3131912

[39]

YamamotoH,SuzukiSW,SuzukiH.The intrinsically disordered protein Atg13 mediates supramolecular assembly of autophagy initiation complexes..Dev Cell2016;38:86-99

[40]

CaoY.Physiological functions of Atg6/Beclin 1: a unique autophagy-related protein..Cell Res2007;17:839-49

[41]

WuJ,SuW,MaH.Molecular cloning, and characterization of rat LC3A and LC3B-two novel markers of autophagosome..Biochem Biophys Res Commun2006;339:437-42

[42]

NixonRA.Lysosomal system pathways: genes to neurodegeneration in Alzheimer’s disease..J Alzheimers Dis2006;9:277-89

[43]

KimHJ,ShimWH.Deficient autophagy in microglia impairs synaptic pruning and causes social behavioral defects..Mol Psychiatry2017;22:1576-84 PMCID:PMC5658669

[44]

LeeKM,LeeJA.Neuronal autophagy and neurodevelopmental disorders..Exp Neurobiol2013;22:133-42 PMCID:PMC3807000

[45]

TangG,KuoSH,RosoklijaG.Loss of mTOR dependent macroautophagy causes autistic-like synaptic pruning deficits..Neuron2014;83:1131-43 PMCID:PMC4159743

[46]

ZhangJ,ZhangQL.PI3K/AKT/mTOR-mediated autophagy in the development of autism spectrum disorder..Brain Res Bull2016;125:152-8

[47]

BowlingH.Shaping dendritic spines in autism spectrum disorder: mTORC1-dependent macroautophagy..Neuron2014;83:994-6

[48]

DanaH,DelibaşıN,BayramR.Disregulation of Autophagy in the Transgenerational Cc2d1a Mouse Model of Autism..Neuromolecular Med2020;22:239-49

[49]

HuberKM,Costa-MattioliM.Dysregulation of mammalian target of rapamycin signaling in mouse models of autism..J Neurosci2015;35:13836-42 PMCID:PMC4604222

[50]

ArnettAB,HoekzemaK,GerdtsJ.The autism spectrum phenotype in ADNP syndrome..Autism Res2018;11:1300-10 PMCID:PMC6203613

[51]

SragovichS,VaisvaserS,HendlerT.The autism mutatedADNP plays a key role in stress response..Transl Psychiatry2019;9:235 PMCID:PMC6751176

[52]

AmramN,SragovichS,KatzJ.Sexual divergence in microtubule function: the novel intranasal microtubule targeting SKIP normalizes axonal transport and enhances memory..Mol Psychiatry2016;21:1467-76

[53]

SragovichS,GozesI.ADNP plays a key role in autophagy: from autism to schizophrenia and Alzheimer’s disease..Bioessays2017;39:

[54]

GozesI.ADNP regulates cognition: a multitasking protein..Front Neurosci2018;12:873 PMCID:PMC6275198

[55]

MalishkevichA,Hacohen-KleimanG,GiladiE.Activity dependent neuroprotective protein (ADNP) exhibits striking sexual dichotomy impacting on autistic and Alzheimer’s pathologies..Transl Psychiatry2015;5:e501 PMCID:PMC4445743

[56]

VargheseM,Jacot-DescombesS,WicinskiB.Autism spectrum disorder: neuropathology and animal models..Acta Neuropathol2017;134:537-66 PMCID:PMC5693718

[57]

De RubeisS.Recent advances in the genetics of autism spectrum disorder..Curr Neurol Neurosci Rep2015;15:36

[58]

DudanovaI,RohlmannA,MisslerM.Deletion of alpha neurexins does not cause a major impairment of axonal pathfinding or synapse formation..J Comp Neurol2007;502:261-74

[59]

HammerM,TuffyLP,TaschenbergerH.Perturbed hippocampal synaptic inhibition and γ-Oscillations in a Neuroligin-4 knockout mouse model of autism..Cell Rep2015;13:516-23 PMCID:PMC5862414

[60]

ChandaS,LeeSJ,SüdhofTC.Pathogenic mechanism of an autism-associated neuroligin mutation involves altered AMPA-receptor trafficking..Mol Psychiatry2016;21:169-77 PMCID:PMC4573762

[61]

DuffneyLJ,WeiJ,ChengJ.Autism-like deficits in Shank3-deficient mice are rescued by targeting actin regulators..Cell Rep2015;11:1400-13 PMCID:PMC4464902

[62]

GoffinD,ZhangL,WangIT.Rett syndrome mutation MeCP2T158A disrupts DNA binding, protein stability, and ERP responses..Nat Neurosci2012;15:274-83 PMCID:PMC3267879

[63]

GrossmanAW,LeeKJ,JunCS.Developmental characteristics of dendritic spines in the dentate gyrus of Fmr1 knockout mice..Brain Res2010;1355:221-7 PMCID:PMC3433497

[64]

FelicianoDM,SuT,BordeyA.Postnatal neurogenesis generates heterotopias, olfactory micronodules, and cortical infiltration following single cell Tsc1 deletion..Hum Mol Genet2012;21:799-810 PMCID:PMC3263992

[65]

DurakO,Kaeser-WooYJ,MartorellAJ.Chd8 mediates cortical neurogenesis via transcriptional regulation of cell cycle and Wnt signaling..Nat Neurosci2016;19:1477-88 PMCID:PMC5386887

[66]

KearneyJA,SmithMR,CumminsTR.A gain-of function mutation in the sodium channel gene Scn2a results in seizures and behavioral abnormalities..Neuroscience2001;102:307-17

[67]

AcetiM,VaissiereT,HuangWC.Syngap1 haploinsufficiency damages a postnatal critical period of pyramidal cell structural maturation linked to cortical circuit assembly..Biol Psychiatry2015;77:805-15 PMCID:PMC4326604

[68]

KaM,DravidSM.Essential roles for ARID1B in dendritic arborization and spine morphology of developing pyramidal neurons..J Neurosci2016;36:2723-42 PMCID:PMC4879215

[69]

MaynardKR.DSCAM contributes to dendrite arborization and spine formation in the developing cerebral cortex..J Neurosci2012;32:16637-50 PMCID:PMC6621782

[70]

EastonCR,MoenSP,BargerZ.Distinct calcium signals in developing cortical interneurons persist despite disorganization of cortex by Tbr1 KO..Dev Neurobiol2016;76:705-20

[71]

JungCH,RoSH,OttoNM.ULK-Atg13-FIP200 complexes mediate mTOR signaling to the autophagy machinery..Mol Biol Cell2009;20:1992-2003 PMCID:PMC2663920

[72]

RussellRC,YuanH,ChangYY.ULK1 induces autophagy by phosphorylating Beclin-1 and activating VPS34 lipid kinase..Nat Cell Biol2013;15:741-50 PMCID:PMC3885611

[73]

RubinszteinDC,LevineB.Autophagy modulation as a potential therapeutic target for diverse diseases..Nat Rev Drug Discov2012;11:709-30 PMCID:PMC3518431

[74]

NixonRA.The role of autophagy in neurodegenerative disease..Nat Med2013;19:983-97

[75]

ShehataM,Okubo-SuzukiR,InokuchiK.Neuronal stimulation induces autophagy in hippocampal neurons that is involved in AMPA receptor degradation after chemical long-term depression..J Neurosci2012;32:10413-22 PMCID:PMC6703735

[76]

YanJ,Court-VazquezB,ZukinRS.Activation of autophagy rescues synaptic and cognitive deficits in fragile X mice..Proc Natl Acad Sci USA2018;115:E9707-16 PMCID:PMC6187122

[77]

RosinaE,SiracusanoM,HollisF.Disruption of mTOR and MAPK pathways correlates with severity in idiopathic autism..Transl Psychiatry2019;9:50 PMCID:PMC6355879

[78]

CuratoloP.Tuberous sclerosis..Handb Clin Neurol2013;111:323-31

[79]

GoordenSM,van der WeerdL,ElgersmaY.Cognitive deficits in Tsc1+/− mice in the absence of cerebral lesions and seizures..Ann Neurol2007;62:648-55

[80]

EhningerD,ShilyanskyC,LiW.Reversal of learning deficits in a Tsc2+/− mouse model of tuberous sclerosis..Nat Med2008;14:843-8 PMCID:PMC2664098

[81]

Chevere-TorresI,SantiniE.Impaired social interactions, and motor learning skills in tuberous sclerosis complex model mice expressing a dominant/negative form of tuberin..Neurobiol Dis2012;45:156-64 PMCID:PMC3225564

[82]

ChenCJ,MaysJ,LuceroR.Therapeutic inhibition of mTORC2 rescues the behavioral and neurophysiological abnormalities associated with Pten-deficiency..Nat Med2019;25:1684-90 PMCID:PMC7082835

[83]

LiebermanOJ,PigulevskiyI,CarbonellJ.mTOR suppresses macroautophagyduring striatal postnatal development and is hyperactive in mouse models of autism spectrum disorders..Front Cell Neurosci2020;14:70 PMCID:PMC7136750

[84]

XingX,WuK,LiX.Suppression of Akt-mTOR pathway rescued the social behavior in Cntnap2-deficient mice..Sci Rep2019;9:3041 PMCID:PMC6395585

[85]

ZhuJW,LiYF,LiuJC.Absence of TRIM32 leads to reduced GABAergic interneuron generation and autism-like behaviors in mice via suppressing mTOR signaling..Cereb Cortex2020;30:3240-58

[86]

OrnoyA,ErgazZ.Prenatal factors associated with autism spectrum disorder (ASD)..ReprodToxicol2015;56:155-69

[87]

RoulletFI,FosterJA.In utero exposure to valproic acid and autism--a current review of clinical and animal studies..Neurotoxicol Teratol2013;36:47-56

[88]

SchneiderT.Behavioral alterations in rats prenatally exposed to valproic acid: animal model of autism..Neuropsychopharmacology2005;30:80-9

[89]

YangEJ,LeeK,KimHS.Early behavioral abnormalities and perinatal alterations of PTEN/AKT pathway in valproic acid autism model mice..PLoS One2016;11:e0153298 PMCID:PMC4829151

[90]

KimJW,KimKC,OhHA.Agmatine rescues autistic behaviors in the valproic acid-induced animal model of autism..Neuropharmacology2017;113:71-81

[91]

SheikhAM,WenG,BrownWT.Cathepsin D, and apoptosis related proteins are elevated in the brain of autistic subjects..Neuroscience2010;165:363-70

[92]

TianY,MoriguchiS,MaoPJ.Melatonin reverses the decreases in hippocampal protein serine/threonine kinases observed in an animal model of autism..J Pineal Res2014;56:1-11

[93]

BozdagiO,BuxbaumJD.Insulin-like growth factor-1 rescues synaptic and motor deficits in a mouse model of autism and developmental delay..Mol Autism2013;4:9 PMCID:PMC3649942

[94]

van Echten-DeckertG,KaracaI.Sphingosine-1-phosphate: boon and bane for the brain..Cell Physiol Biochem2014;34:148-57

[95]

JangS,LeeY,OhS.Modulation of sphingosine 1-phosphate and tyrosine hydroxylase in the stress-induced anxiety..Neurochem Res2011;36:258-67

[96]

WuH,GaoJ,WangJ.Modulation of sphingosine 1-phosphate (S1P) attenuates spatial learning and memory impairments in the valproic acid rat model of autism..Psychopharmacology (Berl)2018;235:873-86

[97]

ZhangY,JiaY,WangL.The Notch signaling pathway inhibitor Dapt alleviates autism-like behavior, autophagy, and dendritic spine density abnormalities in a valproic acid-induced animal model of autism..Prog Neuropsychopharmacol Biol Psychiatry2019;94:109644

[98]

Al-TawashiA,LiuD,QinJ.Protein implicated in nonsyndromic mental retardation regulates protein kinase A (PKA) activity..J Biol Chem2012;287:14644-58 PMCID:PMC3340277

[99]

ManziniMC,ShaheenR,CostanzoSD.CC2D1A regulates human intellectual and social function as well as NF-κB signaling homeostasis..Cell Rep2014;8:647-55 PMCID:PMC4334362

[100]

ZhaoM,ChenZJ.Cc2d1a, a C2 domain containing protein linked to nonsyndromic mental retardation, controls functional maturation of central synapses..J Neurophysiol2011;105:1506-15 PMCID:PMC3075281

[101]

OaksAW,TambunanDE,CostanzoSD.Cc2d1a loss of function disrupts functional and morphological development in forebrain neurons leading to cognitive and social deficits..Cereb Cortex2017;27:1670-85 PMCID:PMC6250986

[102]

RogaevaA.The mental retardation gene CC2D1A/Freud-1 encodes a long isoform that binds conserved DNA elements to repress gene transcription..Eur J Neurosci2007;26:965-74

[103]

Vahid-AnsariF,ManziniMC,HenR.Abrogated freud-1/CC2D1A repression of 5-HT1Aautoreceptors induces fluoxetine-resistant anxiety/depression-like behavior..J Neurosci2017;37:11967-78 PMCID:PMC5722640

[104]

Basel-VanagaiteL,YahavM,AntekiL.The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardation..J Med Genet2006;43:203-10 PMCID:PMC2563235

[105]

Al-TawashiA.Phosphodiesterase activity is regulated by CC2D1A that is implicated in non-syndromic intellectual disability..Cell Commun Signal2013;11:47 PMCID:PMC3704924

[106]

ZamarbideM,Muñoz-LlancaoP,PondHL.Male specific cAMP signaling in the hippocampus controls spatial memory deficits in a mouse model of autism and intellectual disability..Biol Psychiatry2019;85:760-8 PMCID:PMC6474812

[107]

MöhrleD,PeñagarikanoO,AllmanB.What we can learn from a genetic rodent model about autism..NeurosciBiobehav Rev2020;109:29-53

AI Summary AI Mindmap
PDF

31

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/