Expression and processing of mature human frataxin after gene therapy in mice
© 2024. The Author(s)..
Friedreich's ataxia is a degenerative and progressive multisystem disorder caused by mutations in the highly conserved frataxin (FXN) gene that results in FXN protein deficiency and mitochondrial dysfunction. While gene therapy approaches are promising, consistent induction of therapeutic FXN protein expression that is sub-toxic has proven challenging, and numerous therapeutic approaches are being tested in animal models. FXN (hFXN in humans, mFXN in mice) is proteolytically modified in mitochondria to produce mature FXN. However, unlike endogenous hFXN, endogenous mFXN is further processed into N-terminally truncated, extra-mitochondrial mFXN forms of unknown function. This study assessed mature exogenous hFXN expression levels in the heart and liver of C57Bl/6 mice 7-10 months after intravenous administration of a recombinant adeno-associated virus encoding hFXN (AAVrh.10hFXN) and examined the potential for hFXN truncation in mice. AAVrh.10hFXN induced dose-dependent expression of hFXN in the heart and liver. Interestingly, hFXN was processed into truncated forms, but found at lower levels than mature hFXN. However, the truncations were at different positions than mFXN. AAVrh.10hFXN induced mature hFXN expression in mouse heart and liver at levels that approximated endogenous mFXN levels. These results suggest that AAVrh.10hFXN can likely induce expression of therapeutic levels of mature hFXN in mice.
Errataetall: | |
---|---|
Medienart: |
E-Artikel |
Erscheinungsjahr: |
2024 |
---|---|
Erschienen: |
2024 |
Enthalten in: |
Zur Gesamtaufnahme - volume:14 |
---|---|
Enthalten in: |
Scientific reports - 14(2024), 1 vom: 10. Apr., Seite 8391 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Rojsajjakul, Teerapat [VerfasserIn] |
---|
Links: |
---|
Themen: |
---|
Anmerkungen: |
Date Completed 12.04.2024 Date Revised 25.04.2024 published: Electronic UpdateOf: Res Sq. 2023 Dec 28;:. - PMID 38234818 Citation Status MEDLINE |
---|
doi: |
10.1038/s41598-024-59060-0 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM370895630 |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | NLM370895630 | ||
003 | DE-627 | ||
005 | 20240425233752.0 | ||
007 | cr uuu---uuuuu | ||
008 | 240411s2024 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1038/s41598-024-59060-0 |2 doi | |
028 | 5 | 2 | |a pubmed24n1386.xml |
035 | |a (DE-627)NLM370895630 | ||
035 | |a (NLM)38600238 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Rojsajjakul, Teerapat |e verfasserin |4 aut | |
245 | 1 | 0 | |a Expression and processing of mature human frataxin after gene therapy in mice |
264 | 1 | |c 2024 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 12.04.2024 | ||
500 | |a Date Revised 25.04.2024 | ||
500 | |a published: Electronic | ||
500 | |a UpdateOf: Res Sq. 2023 Dec 28;:. - PMID 38234818 | ||
500 | |a Citation Status MEDLINE | ||
520 | |a © 2024. The Author(s). | ||
520 | |a Friedreich's ataxia is a degenerative and progressive multisystem disorder caused by mutations in the highly conserved frataxin (FXN) gene that results in FXN protein deficiency and mitochondrial dysfunction. While gene therapy approaches are promising, consistent induction of therapeutic FXN protein expression that is sub-toxic has proven challenging, and numerous therapeutic approaches are being tested in animal models. FXN (hFXN in humans, mFXN in mice) is proteolytically modified in mitochondria to produce mature FXN. However, unlike endogenous hFXN, endogenous mFXN is further processed into N-terminally truncated, extra-mitochondrial mFXN forms of unknown function. This study assessed mature exogenous hFXN expression levels in the heart and liver of C57Bl/6 mice 7-10 months after intravenous administration of a recombinant adeno-associated virus encoding hFXN (AAVrh.10hFXN) and examined the potential for hFXN truncation in mice. AAVrh.10hFXN induced dose-dependent expression of hFXN in the heart and liver. Interestingly, hFXN was processed into truncated forms, but found at lower levels than mature hFXN. However, the truncations were at different positions than mFXN. AAVrh.10hFXN induced mature hFXN expression in mouse heart and liver at levels that approximated endogenous mFXN levels. These results suggest that AAVrh.10hFXN can likely induce expression of therapeutic levels of mature hFXN in mice | ||
650 | 4 | |a Journal Article | |
650 | 7 | |a Frataxin |2 NLM | |
650 | 7 | |a Iron-Binding Proteins |2 NLM | |
700 | 1 | |a Selvan, Nithya |e verfasserin |4 aut | |
700 | 1 | |a De, Bishnu |e verfasserin |4 aut | |
700 | 1 | |a Rosenberg, Jonathan B |e verfasserin |4 aut | |
700 | 1 | |a Kaminsky, Stephen M |e verfasserin |4 aut | |
700 | 1 | |a Sondhi, Dolan |e verfasserin |4 aut | |
700 | 1 | |a Janki, Peter |e verfasserin |4 aut | |
700 | 1 | |a Crystal, Ronald G |e verfasserin |4 aut | |
700 | 1 | |a Mesaros, Clementina |e verfasserin |4 aut | |
700 | 1 | |a Khanna, Richie |e verfasserin |4 aut | |
700 | 1 | |a Blair, Ian A |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Scientific reports |d 2011 |g 14(2024), 1 vom: 10. Apr., Seite 8391 |w (DE-627)NLM215703936 |x 2045-2322 |7 nnns |
773 | 1 | 8 | |g volume:14 |g year:2024 |g number:1 |g day:10 |g month:04 |g pages:8391 |
856 | 4 | 0 | |u http://dx.doi.org/10.1038/s41598-024-59060-0 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 14 |j 2024 |e 1 |b 10 |c 04 |h 8391 |