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Expression of wild-type human superoxide dismutase-1 in mice causes amyotrophic lateral sclerosis
Umeå universitet, Medicinska fakulteten, Institutionen för medicinsk biovetenskap, Patologi.
Umeå universitet, Medicinska fakulteten, Institutionen för medicinsk biovetenskap, Patologi.
Umeå universitet, Medicinska fakulteten, Institutionen för medicinsk biovetenskap, Patologi.
Umeå universitet, Medicinska fakulteten, Institutionen för farmakologi och klinisk neurovetenskap, Klinisk neurovetenskap.
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2013 (Engelska)Ingår i: Human Molecular Genetics, ISSN 0964-6906, E-ISSN 1460-2083, Vol. 22, nr 1, s. 51-60Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

A common cause of amyotrophic lateral sclerosis (ALS) is mutations in the gene encoding superoxide dismutase-1. There is evolving circumstantial evidence that the wild-type protein can also be neurotoxic and that it may more generally be involved in the pathogenesis of ALS. To test this proposition more directly, we generated mice that express wild-type human superoxide dismutase-1 at a rate close to that of mutant superoxide dismutase-1 in the commonly studied G93A transgenic model. These mice developed an ALS-like syndrome and became terminally ill after around 370 days. The loss of spinal ventral neurons was similar to that in the G93A and other mutant superoxide dismutase-1 models, and large amounts of aggregated superoxide dismutase-1 were found in spinal cords, but also in the brain. The findings show that wild-type human superoxide dismutase-1 has the ability to cause ALS in mice, and they support the hypothesis of a more general involvement of the protein in the disease in humans.

Ort, förlag, år, upplaga, sidor
2013. Vol. 22, nr 1, s. 51-60
Nationell ämneskategori
Neurovetenskaper
Identifikatorer
URN: urn:nbn:se:umu:diva-63578DOI: 10.1093/hmg/dds399ISI: 000312643400004PubMedID: 23026746OAI: oai:DiVA.org:umu-63578DiVA, id: diva2:582102
Tillgänglig från: 2013-01-03 Skapad: 2013-01-03 Senast uppdaterad: 2018-08-19Bibliografiskt granskad
Ingår i avhandling
1. Structural investigation of SOD1 aggregates in ALS: identification of prion strains using anti-peptide antibodies
Öppna denna publikation i ny flik eller fönster >>Structural investigation of SOD1 aggregates in ALS: identification of prion strains using anti-peptide antibodies
2018 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Alternativ titel[sv]
Strukturbestämning av SOD1 aggregat i ALS : identifiering av prionstammar med antipeptidantikroppar
Abstract [en]

Amyotrophic Lateral Sclerosis (ALS) is a fatal neurodegenerative syndrome characterized by progressive degeneration of motor neurons that result in muscle wasting. The symptoms advance gradually to paralysis and eventually death. Most patients suffer from sporadic ALS (sALS) but 10% report a familial predisposition. Mutations in the gene encoding super­oxide dismutase-1 (SOD1) were the first identified cause of ALS. The disease mecha­nism is debated but there is a consensus that mutations in this protein confer a cytotoxic gain of function. SOD1 aggregates in motor neurons are hallmarks of ALS both in patients and in transgenic mouse models expressing a mutated form of human SOD1 (hSOD1). Recently, our group showed that SOD1 aggregates are present also in sALS patients, thus indicating a broader involvement of this protein in ALS. Misfolding and aggregation of SOD1 are dif­ficult to study in vivo since aggregate concentration in the central nervous system (CNS) is exceedingly low. The aim of this thesis was to find a method circumventing this problem to investigate the hSOD1 aggregate structure, distribution and spread in ALS disease.

Many studies provide circumstantial evidence that the wild-type hSOD1 protein can be neurotoxic. We developed the first homozygous mouse model that highly overexpresses the wild-type enzyme. These mice developed an ALS-like syndrome and become terminally ill after around 370 days. Motor neuron loss and SOD1 aggregate accumulation in the CNS were observed. This lends further support to the hypothesis of a more general involve­ment of SOD1 in human disease.

A panel of polyclonal antibodies covering 90% of the SOD1 protein was developed by our laboratory. These antibodies were shown to be highly specific for misfolded SOD1. Aggre­gated hSOD1 was purified from the CNS of terminally ill hSOD1 mice. Disordered segments in aggregated hSOD1 could be identified with these antibodies. Two aggregate strains with different structural architectures, molecular properties, and growth kinetics, were found using this novel method. The strains, denoted A and B, were also associated with different disease progression. Aggregates formed in vitro were structurally different from these strains. The results gave rise to questions about aggregate development and possible prion-like spread. To investigate this, inoculations of purified strain A and B hSOD1 seeds was performed in lumbar spinal cords of 100-day old mice carrying a hSOD1G85R mutation. Mice seeded with A or B aggregates developed premature signs of ALS and became terminally ill 200 days earlier than mice inoculated with control preparation. Interestingly, a tem­plated spread of aggregates along the neuraxis was concomitantly observed, with strain A and B provoking the buildup of their respective hSOD1 aggregate structure. The phenotypes initiated by the A and B strains differed regarding progression rates, distribution, end-stage aggregate levels, and histopathology. To further establish the importance of hSOD1 aggregates in human disease, purification and inoculation of aggregate seeds from spinal cords of ALS patients and mice carrying the hSOD1G127X mutation were performed. Inoculation of both human and mouse seeds as described above, induced strain A aggregation and premature fatal ALS-like disease.

In conclusion, the data presented in this thesis provide a new, straightforward method for characterization of aggregate strains in ALS, and plausibly also in other neurodegen­erative diseases. Two different prion strains of hSOD1 aggregates were identified in mice that resulted in ALS-like disease. Emerging data suggest that prion-like growth and spread of hSOD1 aggregation could be the primary pathogenic mechanism not only in hSOD1 transgenic models, but also in human ALS.

Ort, förlag, år, upplaga, sidor
Umeå: Umeå universitet, 2018. s. 94
Serie
Umeå University medical dissertations, ISSN 0346-6612 ; 1966
Nyckelord
ALS, SOD1, prion, motor neuron disease, neurodegeneration, strain, seeding, protein aggregation, transgenic mice, peptide antibodies
Nationell ämneskategori
Neurovetenskaper Neurologi
Forskningsämne
neurologi
Identifikatorer
urn:nbn:se:umu:diva-150911 (URN)978-91-7601-907-8 (ISBN)
Disputation
2018-09-14, NUS 6A–L - Biomedicinhuset, Major Groove, Umeå, 09:00 (Svenska)
Opponent
Handledare
Tillgänglig från: 2018-08-22 Skapad: 2018-08-19 Senast uppdaterad: 2018-08-24Bibliografiskt granskad

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Graffmo, Karin S.Forsberg, KarinBergh, JohanBirve, AnnaZetterström, PerAndersen, Peter M.Marklund, Stefan L.Brännström, Thomas

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Graffmo, Karin S.Forsberg, KarinBergh, JohanBirve, AnnaZetterström, PerAndersen, Peter M.Marklund, Stefan L.Brännström, Thomas
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