Wild-type Huntingtin, a billion-year experiment. Elena Cattaneo University of Milano and National Institute of Molecular Genetics

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Transkript:

Wild-type Huntingtin, a billion-year experiment Elena Cattaneo University of Milano and National Institute of Molecular Genetics

A cyclopean endeavor 1979 1983 1993 HTT gene Chr4 Exon1 (67 exons) ~180 kb CAG N17 region PolyQ Proline-rich domain 3 exon1 8-35 Q normal repeats 36-39 Q reduced penetrance 40-55 Q repeats adult onset 60-180 Q repeats juvenile onset gene protein ~340 KDa

Huntington s Disease Autosomal dominant, neurodegenerative disease Movement disorder, cognitive impairment, mood disturbances Midlife onset (juvenile and adult) Mortality 15-20 years following onset Degeneration of striatal medium spiny Cortical atrophy

HTT expression in tissues HTT is broadly expressed Cerebral cortex However, expression is higher in the nervous system than in other tissues Within the brain it is highly expressed in cerebral cortex

HTT sub-cellular localization Hilditch-Maguire et al., H M Gen 2000 Hoffner et al., J Cell Sci 2002 Kegel et al., J Biol Chem 2002 Panov et al., Nat Neurosci 2002 Strehlow et al., Hum Mol Genet 2007 DiFiglia et al., Neuron 1995 Velier et al., Exp Neurol 1998 Steffan et al., PNAS 2000 Smith et al., Cell Mol Life Sci 2005 Caviston et al., Trends Cell Biol 2009 HTT Mitochondria HTT Golgi complex HTT Endoplasmic reticulum Nucleus Vesicular structures HTT Microtubules Vesicular transport HTT Neurite HTT Synapse ~50% of wild-type HTT mrna localizes to the nucleus This nuclear localization is observed only in neuronal cells. Didiot et al., Cell Rep. 2018

Agenda Mutant Htt toxicity What is the evidence that wthtt is important? Is there loss of wthtt function in HD?

Agenda Mutant Htt toxicity What is the evidence that wthtt is important? Is there loss of wthtt function in HD?

1 Cell 2000 E15 +Doxy P0 muhtt off muhtt on muhtt on 18w muhtt off +Doxy 34w Turning off muhtt is sufficient to reverse the disease in mice Neuropathology & motor abnormalities ST, nuclear aggregates CX, extranuclear aggregates control HD94 gene on gene off control HD94 gene on gene off CO HD CO HD control HD94 gene on gene off

2 Neuron 2010 Nat Med 2009 24OHC Glu Glu Glu Lipid rafts Synaptic NMDAr Low conc Memantine blocks extrasynaptic NMDARs and restores neuroprotective CREB-PGC1a PC7 Syn- NMDA Trkb neuroprotection Glu SAP97 P-CREB PGC-1a neurotoxicity BDNF DARPP32 Glu Extrasynaptic NMDAr

3 2014 BACHD; Rgs9-Cre Tg Reduction in striatum BACHD; Emx1-Cre Tg Reduction in cortex BACHD; Emx1-Cre Tg; Rgs9-Cre Tg; Reduction in cortex and striatum Reduction of muhtt in ST Reduction of muhtt in CX Reduction of muhtt in ST+CX Reduction of muhtt in ST Cell PSD-95 Actn2 synaptophysin Cell autonomous toxicity of muhtt in striatum PSD NMDAr currents

3 2014 BACHD; Rgs9-Cre Tg Reduction in striatum BACHD; Emx1-Cre Tg Reduction in cortex BACHD; Emx1-Cre Tg; Rgs9-Cre Tg; Reduction in cortex and striatum Reduction of muhtt in ST Reduction of muhtt in CX Reduction of muhtt in ST+CX Reduction of muhtt in CX synaptophysin Cell PSD PSD-95 Actn2 NMDAr currents sepsc higher sipsc lower Non-cell autonomous toxicity of muhtt in striatum

Astrocytes, additional players at the HD cortico-striatal synapse 4 LXR SRE 24OHC apoe Glu Lipid rafts PC7 Glu Trkb Syn- NMDA Glu neuroprotection Cholesterol biosynthesis Glu In HD SAP97 P-CREB PGC-1a neurotoxicity BDNF DARPP32 Glu Sipione, Hum Mol Gen 2002

Astrocytes, additional players at the HD cortico-striatal synapse Hypothesis 2002 Sipione, Hum Mol Gen 2002 4 Molecular mechanisms 2005-2015 Valenza, J. Neurosci 2005 Bobrowska, PlosOne 2012 Lee, Neuron 2014 Valenza, Cell Death Differ 2015 Biological relevance 2007-2017 Trushina, Hum Mol Gen 2006 Valenza, Hum Mol Gen 2007 Valenza, Neurobiol Dis 2007 Futter, J. Med gen 2009 Valenza, Neurosci 2010 Luthi-Carter, PNAS 2010 Del Toro, J. Neurochem 2010 Xiang, J. Neurosci 2011 Koga, J. Neurosci 2011 Marullo, PlosHD 2012 Ritch, Mol Cell Neurosci. 2012 Trushina, Hum Mol Gen 2013 Gao, Biochemistry 2015 Kreilus, Journal of HD 2015 Shankaran, Neurobiol Dis 2017 Boussicault, Biochemie, 2018 24OH as a Biomarker 2008-2013 Leoni, Brain 2008 Leoni, Neurosci Lett 2011 Leoni, Neurobiol Dis 2013 Mariotti, Longitudinal studies on-going Therapeutical strategies (nanoparticles mediated cholesterol delivery; CYP46 gene therapy) 2015-2019 Valenza, EMBO Mol Med, 2015 Manuscript in preparation (Cattaneo Lab) Boussicault, Brain, 2016 Kacher, Brain, 2019

Conclusions muhtt toxicity causes nuclear, cytoplasmic and mitochondrial pathology; it affects neurons and astrocytes; it acts in a cell autonomous and non-cell autonomous manner; toxicity can be reversed by turning off muhtt expression; in a disease-modifying therapy both striatum and cortex should be targeted.

Agenda Mutant Htt toxicity What is the evidence that wthtt is important? Is there loss of wthtt function in HD?

nature s evidence evolution experimental evidence wthtt genetics human studies wthtt HD background

MATLEKLMKAFESLKSFQQQQQQQQQQQQQQQQQQQQQQQPPPPPPPPPPPQLPQPPPQAQPLLPQ PQPPPPPPPPPPGPAVAEEPLHRPKKELSATKKDRVNHCLTICENIVAQSVRNSPEFQKLLGIAME LFLLCSDDAESDVRMVADECLNKVIKALMDSNLPRLQLELYKEIKKNGAPRSLRAALWRFAELAHL VRPQKCRPYLVNLLPCLTRTSKRPEESVQETLAAAVPKIMASFGNFANDNEIKVLLKAFIANLKSS SPTIRRTAAGSAVSICQHSRRTQYFYSWLLNVLLGLLVPVEDEHSTLLILGVLLTLRYLVPLLQQQ VKDTSLKGSFGVTRKEMEVSPSAEQLVQVYELTLHHTQHQDHNVVTGALELLQQLFRTPPPELLQT LTAVGGIGQLTAAKEESGGRSRSGSIVELIAGGGSSCSPVLSRKQKGKVLLGEEEALEDDSESRSD VSSSALTASVKDEISGELAASSGVSTPGSAGHDIITEQPRSQHTLQADSVDLASCDLTSSATDGDE EDILSHSSSQVSAVPSDPAMDLNDGTQASSPISDSSQTTTEGPDSAVTPSDSSEIVLDGTDNQYLG LQIGQPQDEDEEATGILPDEASEAFRNSSMALQQAHLLKNMSHCRQPSDSSVDKFVLRDEATEPGD QENKPCRIKGDIGQSTDDDSAPLVHCVRLLSASFLLTGGKNVLVPDRDVRVSVKALALSCVGAAVA LHPESFFSKLYKVPLDTTEYPEEQYVSDILNYIDHGDPQVRGATAILCGTLICSILSRSRFHVGDW MGTIRTLTGNTFSLADCIPLLRKTLKDESSVTCKLACTAVRNCVMSLCSSSYSELGLQLIIDVLTL RNSSYWLVRTELLETLAEIDFRLVSFLEAKAENLHRGAHHYTGLLKLQERVLNNVVIHLLGDEDPR VRHVAAASLIRLVPKLFYKCDQGQADPVVAVARDQSSVYLKLLMHETQPPSHFSVSTITRIYRGYN LLPSITDVTMENNLSRVIAAVSHELITSTTRALTFGCCEALCLLSTAFPVCIWSLGWHCGVPPLSA SDESRKSCTVGMATMILTLLSSAWFPLDLSAHQDALILAGNLLAASAPKSLRSSWASEEEANPAAT KQEEVWPALGDRALVPMVEQLFSHLLKVINICAHVLDDVAPGPAIKAALPSLTNPPSLSPIRRKGK EKEPGEQASVPLSPKKGSEASAASRQSDTSGPVTTSKSSSLGSFYHLPSYLKLHDVLKATHANYKV TLDLQNSTEKFGGFLRSALDVLSQILELATLQDIGKCVEEILGYLKSCFSREPMMATVCVQQLLKT LFGTNLASQFDGLSSNPSKSQGRAQRLGSSSVRPGLYHYCFMAPYTHFTQALADASLRNMVQAEQE NDTSGWFDVLQKVSTQLKTNLTSVTKNRADKNAIHNHIRLFEPLVIKALKQYTTTTCVQLQKQVLD LLAQLVQLRVNYCLLDSDQVFIGFVLKQFEYIEVGQFRESEAIIPNIFFFLVLLSYERYHSKQIIG IPKIIQLCDGIMASGRKAVTHAIPALQPIVHDLFVLRGTNKADAGKELETQKEVVVSMLLRLIQYH QVLEMFILVLQQCHKENEDKWKRLSRQIADIILPMLAKQQMHIDSHEALGVLNTLFEILAPSSLRP VDMLLRSMFVTPNTMASVSTVQLWISGILAILRVLISQSTEDIVLSRIQELSFSPYLISCTVINRL RDGDSTSTLEEHSEGKQIKNLPEETFSRFLLQLVGILLEDIVTKQLKVEMSEQQHTFYCQELGTLL MCLIHIFKSGMFRRITAAATRLFRSDGCGGSFYTLDSLNLRARSMITTHPALVLLWCQILLLVNHT DYRWWAEVQQTPKRHSLSSTKLLSPQMSGEEEDSDLAAKLGMCNREIVRRGALILFCDYVCQNLHD SEHLTWLIVNHIQDLISLSHEPPVQDFISAVHRNSAASGLFIQAIQSRCENLSTPTMLKKTLQCLE GIHLSQSGAVLTLYVDRLLCTPFRVLARMVDILACRRVEMLLAANLQSSMAQLPMEELNRIQEYLQ SSGLAQRHQRLYSLLDRFRLSTMQDSLSPSPPVSSHPLDGDGHVSLETVSPDKDWYVHLVKSQCWT RSDSALLEGAELVNRIPAEDMNAFMMNSEFNLSLLAPCLSLGMSEISGGQKSALFEAAREVTLARV SGTVQQLPAVHHVFQPELPAEPAAYWSKLNDLFGDAALYQSLPTLARALAQYLVVVSKLPSHLHLP PEKEKDIVKFVVATLEALSWHLIHEQIPLSLDLQAGLDCCCLALQLPGLWSVVSSTEFVTHACSLI YCVHFILEAVAVQPGEQLLSPERRTNTPKAISEEEEEVDPNTQNPKYITAACEMVAEMVESLQSVL ALGHKRNSGVPAFLTPLLRNIIISLARLPLVNSYTRVPPLVWKLGWSPKPGGDFGTAFPEIPVEFL QEKEVFKEFIYRINTLGWTSRTQFEETWATLLGVLVTQPLVMEQEESPPEEDTERTQINVLAVQAI TSLVLSAMTVPVAGNPAVSCLEQQPRNKPLKALDTRFGRKLSIIRGIVEQEIQAMVSKRENIATHH LYQAWDPVPSLSPATTGALISHEKLLLQINPERELGSMSYKLGQVSIHSVWLGNSITPLREEEWDE EEEEEADAPAPSSPPTSPVNSRKHRAGVDIHSCSQFLLELYSRWILPSSSARRTPAILISEVVRSL LVVSDLFTERNQFELMYVTLTELRRVHPSEDEILAQYLVPATCKAAAVLGMDKAVAEPVSRLLEST LRSSHLPSRVGALHGVLYVLECDLLDDTAKQLIPVISDYLLSNLKGIAHCVNIHSQQHVLVMCATA FYLIENYPLDVGPEFSASIIQMCGVMLSGSEESTPSIIYHCALRGLERLLLSEQLSRLDAESLVKL SVDRVNVHSPHRAMAALGLMLTCMYTGKEKVSPGRTSDPNPAAPDSESVIVAMERVSVLFDRIRKG FPCEARVVARILPQFLDDFFPPQDIMNKVIGEFLSNQQPYPQFMATVVYKVFQTLHSTGATWSLSC FFVSASTSPWVAAILPHVISRMGKLEQVDVNLFCLVATDFYRHQIEEELDRRAFQSVLEVVAAPGS 67 exons Human HTT chr4 3144 aa 340 KDa 1 CAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAACAG

MDLIRGLDILSASPIDTEDQNLRKEKIEACRTISEQICAPSLRNTADFPRFLSIAISLLLRAHGD KDLNVYSVAEESLNRTIKILVYSYHERILFELFKVLKGKPHQHNNEKRLSTNLTDHLSQNSVTPS VPTTPNYQQSPSTQSPSHSTSNSSNNLYNNFSSNSNSNSNSNSNSSSNNNSGNTTPGNNTNNSNG NANSIFNTANQILSKPFPLKSQRIALIKFGEICSFIRPSKCRKYILSLVPPINSLLSIIEDESLQ ESISISMENISKILIPYLKENEVHQLIDLFSRNLQQPSAAVRRAASLSITSICRYHPRPLFEFTI EFLYNFTFPNSPPISSITSASCIPASSNTNTLQNSKILGVLFSYLQLIKLAEELSSNDIKILDGF SLKIQFFVHFILKYIQVPIDGEPYDHNIVGLSLELLQQLLVTFGPYEYSWPKPLVREVIAQLRHL CFNQQSSIRVSLKAVVLNCLAQSVKFFPKLFNDEFFKHQPSTIDSNTVTSAEDHICRDYLLNISP SDLNFKLFTPITQQQQQQQQQQQQQQQQQQQHNLTSSTMSGINSTTGVSNHTFSLEPKEEFLYYL NDSDPLLRGGTALMIGCLIRGYLETDHITSNQIYPTNIALLEDNLSIPTLLIFLLRALMDSSSIT AKLACTGISECLPILSQSKFSDWALVTLRHLLCVSSSTYWLVKLEILETLSMIDYIVIEYLEQNI QQKSNVMNVVINGPNLSISTSSIKINENNNNSNNSNNNKNNSETGGAVAIPIQSKVLDFLIEQLS DNDFRVRNSAGKSLVRVIPKLVFTAPLERHSMKGISSKVRETFDVQDYENTVLRKRKIFANLSHV IGLLVNQLSNPHPDDKIRGCYGALNLICKTYSFPPDTPEQCRTLSSVLANPMLSFVGDILPLALD RVGLTWVATDFDVHIDIIEILGYLSRGAENVLGTYCHNVLRHIVRIINIATNIIQFRPTPPLKEV KSNPSGIHVNSPLLKAPTHLGSFTHSIHYIKLYSKLLTARINSITIFGIDRFSQLRQACFETLSV MLKCAGKTILPYTEEIIGYLTTHFEQEPVSVIKCINELFLVTMKPTPIVSISSLSQKSRDLNIGG GFISTGGGGGGGSGGINSSSSSLKQYEPRSIESHSSSSNSHDEMFLNSRSVFSSLLTFGTPNLKQ HYDFINEVPSSHNINYSYSNSEINRIISNEDRKLNFKLFEPLIIGSMIEYQTTHSHELKIAILLM LSKLSKFGLDLSLFDKENHFPTYFIEELKETHCLLSKPNQVLSYSYDLLGSMFIYRKLFPDSSVS IDDIKKLFFQPPPQQQQQTNQNKSQSLNSTPNISSNNNNNNNNNNNNNNNNNNNNNNNSNSSQSL NNSTVIGNNSSHPYSYTIPTIIENCHSFVRYLYDPNDKYPDTDFRERFLSFLLSNLQYSQTIDIL ILIVTIVQPNSTLHQKFSQQISHQLFTNLSLGDSPFFIINSIEEVERLYVLIDKLHSSSLSAARW ADALLSVSPQFVNKSTSSSSSSSSTATSPSSSSSSTTTTTTTSTNTTTTTPSDPLIRKRILLLRE SILEAYELRWLPPLLVLLRTGCKLPEEARISAARQSRFLSNHDNKHQPGPSAAIISTLLLKLIRN AVSVFSLYKPKNVLFTQLINHLLYYSSIFFNKNLVPHISAQSLSNSPNFGATNTTTGSGSVSPLS SSSSSTITVTTMAMGSSLMKQPSSSLLLSPTVGGSSSTINLFMDSLKGILALDNGTIIQEITTSL LSYGGTSTSIHAVKLLLLLGRLPNQQVIEGADLVWKQYALSNNWQSCGCEHFLTHHIIFLLYCQS IVVLKSQNIELSETFLDKIVLLINESTVKKLIEFLVKGGSNSDQNQYIEIFTQHLVKIFSRVSNS LDLRKKQKLLRLLSYLPANRETLELLIVNFLQTDDISLQVSGERILNLNINNLIETYGPQNSLEI IQELYQIFMSNFVKSTTNQSVQSLFLKLIKNLSPSSAYQGITPTHNNVIEKLKEKELTNNNNNNN NNIIEKEEEEKEKEKEKVKEEEEGNNIEKLIQLQIETIKKNNQISDLKTVPWDYFVELIKSRYYS NNLNQHSFNNISILSQIDKDATISLLESKSLDGTLLPAFISSVYSLEFQDEIQAYLLKKVDTLLG LAGEIGTDPLKGGPPFLSDSVWDELRETTRCLSNFINKFGLGELCESKLLKVSTWAFIESFRRWR AEIINPYDFKLVLELSRSIILKSTASILTITDDSEWCSLLLCLYKLYCLVIRPHFGYISGQRELE ENFSQDPTQISLTQSNEMIKFLVSLLTNVKSYTPMPGSHIGQLIFDSFIRAIIPLSTKAFDFIYP Dicty HTT TVSTSSEDEFGGGIIPNCPIFSSNVSPEQNIKALVSFIHFVDIDDEFKFKQIWEMLEPIFVSPLG DAEMGSDEITEECKCLSLSGMATMIIKVCFEVTGVNSQVNLLETSTIPKSTYNHIPREKDLMFLN TPTGKKLNHLLSTIYGDMPQSELPLGGAIESVSSSSSMFGESSGNHQNMSSSSLSAYHFNIERSF chr2 SSNQFGSDQISLSDLRLFKTPYFIGVNFTPIIQKLLESFESFLVNPMCPPMLKKDILKSTVLLSD LFNREQVIWMFKTFTTIYAQDEIDDFLLKQHLILGICKGIAILQTPPNVGDSNAHSVGIFEMLKS 4 exons ALDHQNISLQVSALDGILYLLEGKVNKYIQGSLLQFLFRWIPTRLSSVPFPPVSLTLRVLATMFL MIEQYSREAEETLFTKRAVTTCIQLGQQQSTPVPIVYGVFRGLDRLLVSFSLSHSQRELISHFSL 3095 aa KSLPSENPIRSLLALGLMVTCIYTGDETGINSPSFTKSSISSIGSGGVNSLTAFEGSFSSSSIES PLNSALDSVMSSFIMDDNYSGSGGNSLINGGGGGDPLSSLDRQKFSRVNNMEKVKMLFDKIRLVS 330 KDa HFSYESHVLSEVLPVVIVDLFPSVDQVLSFILGEFLKQSKTNSKLMCQIISKVFDFLVENDTSEN TNQHLINYWIIICLQNFFQIQNPTHCLWALTYLFLTSSPKRSFKLLESEFASKIQTNEKLFIIIA Myre, PLOS Genetics, 2011 1

HTT CAG along the human lineage 1 no CAG protostoms deuterostoms 9-35 CAG 15 CAG 12 CAG 10 CAG 8 CAG 7 CAG 4 CAG 2 CAG 2 CAG no CAG Tartari, Mol. Biol. Evol, 2008; more work ongoing a billion years ago Dictyostelium Discoideum

HTT polyq along the human lineage 1

An evolutionary recent neuroepithelial cell adhesion function of huntingtin implicates ADAM10-Ncadherin 1 Valentina Lo Sardo, Chiara Zuccato, Germano Gaudenzi, Barbara Vitali, Catarina Ramos, Marzia Tartari, Michael A Myre, James A Walker, Anna Pistocchi, Luciano Conti, Marta Valenza, Binia Drung, Boris Schmidt, James Gusella, Scott Zeitlin, Franco Cotelli & Elena Cattaneo 2012 unpublished

An evolutionary recent neuroepithelial cell adhesion function of huntingtin implicates ADAM10-Ncadherin 1 Valentina Lo Sardo, Chiara Zuccato, Germano Gaudenzi, Barbara Vitali, Catarina Ramos, Marzia Tartari, Michael A Myre, James A Walker, Anna Pistocchi, Luciano Conti, Marta Valenza, Binia Drung, Boris Schmidt, James Gusella, Scott Zeitlin, Franco Cotelli & Elena Cattaneo 2012 unpublished

An evolutionary recent neuroepithelial cell adhesion function of huntingtin implicates ADAM10-Ncadherin 1 Valentina Lo Sardo, Chiara Zuccato, Germano Gaudenzi, Barbara Vitali, Catarina Ramos, Marzia Tartari, Michael A Myre, James A Walker, Anna Pistocchi, Luciano Conti, Marta Valenza, Binia Drung, Boris Schmidt, James Gusella, Scott Zeitlin, Franco Cotelli & Elena Cattaneo 2012 Lo Sardo, Ant. Neurosci 2012

2 J. Med. Gen, 2013 n. alleles number of CAG repeats CAG allele length 1/17 individuals carries an IA (27-35 CAG) = 5.8% also see Rubinsztein, Nature Genetics, 1994

Plos One, 2012 3 MRI scan on 278 subjects

JNR, 2017 4 EBioMedicine, 2018

Conclusions muhtt toxicity causes nuclear, cytoplasmic and mitochondrial pathology; it affects neurons and astrocytes; it acts in a cell autonomous and non-cell autonomous manner; toxicity can be reversed by turning off muhtt expression; in a disease-modifying therapy both striatum and cortex should be targeted. for a billion years nature has not eliminated huntingtin but implemented its functions by lengthening its CAG

nature s evidence evolution experimental evidence wthtt genetics human studies wthtt HD background

wthtt is important during development Knockout is embryonic lethal Heterozygote demonstrates neurodegeneration in subthalatic nucleus and globus pallidus Postnatal Htt reduction detrimental Mutant Htt retains normal function

What is the evidence that wthtt continues to be required throughout life to support neuronal survival and homeostasis? What happens if we reduce wthtt level in the adult brain under stressed conditions (HD)?

J. of Neurochem 2003 mouse wthtt mouse wthtt human wthtt 1 Yac18 mouse line Depletion of huntingtin in neurologic disease models featuring caspase activation Wild-type huntingtin overexpression reduces the lesion volume after post-ischemic injury

2 J. of Neurochem 2006 mouse wthtt mouse wthtt human wthtt Yac18 mouse line wthtt is neuroprotective in vitro Over-expression of wthtt in YAC18 mice causes decreased neurodegeneration after QA in a dose-dependent manner

Plos Genetics, 2017 3 Long term global HTT loss no TM TM@3 mo Reduced longevity TM@6 mo TM@9 mo months

Plos Genetics, 2017 3 Long term global HTT loss no TM TM@3 mo Reduced longevity TM@6 mo TM@9 mo months Motor and behavioral deficit Brain atrophy Calcification Iron depletion

Plos Genetics, 2017 3 Long term global HTT loss no TM TM@3 mo Reduced longevity TM@6 mo TM@9 mo months wthtt elimination causes the same time-dependent defects regardless of the stage at which the animals were treated Defects are time dependent

4 HMG, 2005 no mouse wthtt wthtt no mouse mouse wthtt wthtt Yac18 (human) Yac128 (human) Yac 18/128 mouse line Loss of wild-type htt expression in YAC128 mice results in mild worsening of behavioural phenotype Loss of wild-type htt has a modest effect on striatal neuropathology in YAC128 mice Time on rotarod (sec) Time on rotarod (sec) YAC128 mice show a male specific survival deficit that is exacerbated by the loss of wthtt expression

5 BMC Neuroscience 2006 no mouse wthtt no mouse wthtt Yac128 (human) Yac128 mouse line Over-expression of wild-type HTT results in mild improvements in striatal neuropathology in YAC128 mice Striatal volume Striatal neuronal counts wt Yac 18 Yac 128 Striatal DARPP32 expression Yac 18/ 128 wt Yac 18 Yac 128 Yac 18/ 128 Striatal neuronal croos sectional area wt Yac 18 Yac 128 Yac 18/ 128 wt Yac 18 Yac 128 Yac 18/ 128

Conclusions muhtt toxicity causes nuclear, cytoplasmic and mitochondrial pathology; it affects neurons and astrocytes; it acts in a cell autonomous and non-cell autonomous manner; toxicity can be reversed by turning off muhtt expression; in a disease-modifying therapy both striatum and cortex should be targeted. for a billion years nature has not eliminated huntingtin but implemented its functions by lengthening its CAG HTT exerts different functions in the developing and adult brain In the adult brain wthtt continues to be necessary and is neuroprotective while muhtt is unable to support, for example, BDNF production.

Agenda Mutant Htt toxicity What is the evidence that wthtt is important? Is there loss of wthtt function in HD?

wthtt is antiapoptotic while muhtt increases apoptosis J. Neurosci 2000 1 33 C in serum 39 C in SFM ST14A cells

wthtt (but not mutant) stimulates BDNF production % of BDNF 300 2 200 100 0 BDNF % of BDNF CX gene trasncription CX ERK CREB Neuroprotection BDNF mrna over actin TrkB 100 0 transport Science 2001 ST +/+ +/- -/-

BDNF production and delivery is dependent on wthtt and is reduced in HD HD cell lines > 10 manuscripts show reduction in BDNF BDNF gene trasncription transport HD mouse models > 30 manuscripts show reduction in BDNF level in brain in 5 transgenic models (R6/2; R6/1; YAC72, BACHD;N171-82Q) 3 knock-in models (Hdh 111/111 ; Hdh 150/150 ; ZQ175) HD human brain 3 papers show decreased BDNF levels TrkB ERK CREB Neuroprotection Human HD neurons from pluripotent stem cells New unpublished data

There is a BDNF pathology in HD which is due to loss of wthtt function 2 Emx1-BDNF KO HD-like behavioral phenotype Gene expression changes similar to the ones in human HD caudate Baquet, J. Neurosci, 2004 Strand, J. Neurosci, 2007 BDNF +/- R6/1 Earlier onset, worsening of the behavioral, motor phenotype Loss of striatal enkephalinpositive neurons Canals, J. Neurosci, 2004 CamKIIα BDNF Tg;R6/1 Improvement of behavioral and motor phenotype Improvement of neuropathology and BDNF-mediated signalling Gharami, J. Neurochem, 2008 CamKIIα BDNF Tg;YAC128 Less atrophy of striatal neurons Improvements of motor dysfunction Xie, J. Neurosci, 2010

conto There is a BDNF/NRSE pathology in HD which is due to loss of wthtt function 2 several other neuronal genes several other neuronal genes

wthtt (but not mutant) inhibits ADAM10 An evolutionary recent neuroepithelial cell adhesion function of huntingtin implicates ADAM10-Ncadherin Valentina Lo Sardo, Chiara Zuccato, Germano Gaudenzi, Barbara Vitali, Catarina Ramos, Marzia Tartari, Michael A Myre, James A Walker, Anna Pistocchi, Luciano Conti, Marta Valenza, Binia Drung, Boris Schmidt, James Gusella, Scott Zeitlin, Franco Cotelli & Elena Cattaneo 2012 3 Hdh +/+ Hdh -/-

wthtt (but not mutant) inhibits ADAM10 An evolutionary recent neuroepithelial cell adhesion function of huntingtin implicates ADAM10-Ncadherin Valentina Lo Sardo, Chiara Zuccato, Germano Gaudenzi, Barbara Vitali, Catarina Ramos, Marzia Tartari, Michael A Myre, James A Walker, Anna Pistocchi, Luciano Conti, Marta Valenza, Binia Drung, Boris Schmidt, James Gusella, Scott Zeitlin, Franco Cotelli & Elena Cattaneo 2012 3 Hdh +/+ Hdh -/- Hdh -/- Cells wthtt wthtt ADAM10 CTRL detectable by WB Ncadherin HD-60#5 ADAM10 CTF1

wthtt (but not mutant) inhibits ADAM10 An evolutionary recent neuroepithelial cell adhesion function of huntingtin implicates ADAM10-Ncadherin Valentina Lo Sardo, Chiara Zuccato, Germano Gaudenzi, Barbara Vitali, Catarina Ramos, Marzia Tartari, Michael A Myre, James A Walker, Anna Pistocchi, Luciano Conti, Marta Valenza, Binia Drung, Boris Schmidt, James Gusella, Scott Zeitlin, Franco Cotelli & Elena Cattaneo 2012 3 Hdh +/+ Adult cko brain wthtt CTRL HD-60#5 ADAM10 CTF1

wthtt (but not mutant) inhibits ADAM10 3 Journal Clinical Investigation 2019 Adult cko brain Adult HD brain wthtt muhtt CTRL HD-60#5 ADAM10 CTF1 ADAM10 CTF1

Conclusions muhtt toxicity causes nuclear, cytoplasmic and mitochondrial pathology; it affects neurons and astrocytes; it acts in a cell autonomous and non-cell autonomous manner; toxicity can be reversed by turning off muhtt expression; in a disease-modifying therapy both striatum and cortex should be targeted. for a billion years nature has not eliminated huntingtin but implemented its functions by lengthening its CAG HTT exerts different functions in the developing and adult brain In the adult brain wthtt continues to be necessary and is neuroprotective while muhtt is unable to support, for example, BDNF production. Some phenotypes in HD are due to loss of wthtt function,

Extrasyn-NMDA We need to preserve wthtt function in the HD brain wthtt RE1 BDNF Huntingtin BDNF prom. BDNF LXR SRE REST apoe 24OHC Glu Lipid rafts Dopamine Glu Glu wthtt Dopamine receptors PC7 m-adam10 SAP97 Syn- NMDA Trkb P-CREB neuroprotection neurotoxicity Glu BDNF DARPP32 Glu

Our lab in Milano Chiara Zuccato Associate Professor Dario Besusso Postdoctoral Fellow Vittoria Bocchi Postdoctoral Fellow Marta Valenza Researcher Elena Vezzoli Postdoctoral Fellow Martina Zobel Postdoctoral Fellow Giorgia Ferlazzo Postdoctoral Fellow Paola Conforti Specialized technologist Maura Galimberti Postdoctoral Fellow Giulia Birolini PhD Student Raffaele Iennaco Postdoctoral Fellow Silvia Brocchetti PhD Student Andrea Scolz Junior Fellow Andrea Cossu Junior Fellow MANAGEME NT & PUBLIC OUTREACH Gianni Munizza Project Manager Federico Tili Lab Manager Tiziana Turrisi Grant & Pers. Manager STUDENTS: Pia Rivetti Postdoctoral Fellow Manuel Cernigoj PhD Student Camilla Trovesi Postdoctoral Fellow Ilaria Campus Junior Fellow Tiziana Lischetti Ayat Ahmed Claudio Cappadona Arianna Ferrari Ivan Lombardi Manuela Magni Elena Melacini Marta Vittani