Excess PrPC inhibits muscle cell differentiation via miRNA-enhanced liquid-liquid phase separation implicated in myopathy
© 2023. The Author(s)..
The cellular prion protein (PrPC) is required for skeletal muscle function. Here, we report that a higher level of PrPC accumulates in the cytoplasm of the skeletal muscle of six myopathy patients compared to controls. PrPC inhibits skeletal muscle cell autophagy, and blocks myoblast differentiation. PrPC selectively binds to a subset of miRNAs during myoblast differentiation, and the colocalization of PrPC and miR-214-3p was observed in the skeletal muscle of six myopathy patients with excessive PrPC. We demonstrate that PrPC is overexpressed in skeletal muscle cells under pathological conditions, inhibits muscle cell differentiation by physically interacting with a subset of miRNAs, and selectively recruits these miRNAs into its phase-separated condensate in living myoblasts, which in turn enhances liquid-liquid phase separation of PrPC, promotes pathological aggregation of PrP, and results in the inhibition of autophagy-related protein 5-dependent autophagy and muscle bundle formation in myopathy patients characterized by incomplete muscle regeneration.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2023 |
---|---|
Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:14 |
---|---|
Enthalten in: |
Nature communications - 14(2023), 1 vom: 08. Dez., Seite 8131 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Tao, Jing [VerfasserIn] |
---|
Links: |
---|
Themen: |
Journal Article |
---|
Anmerkungen: |
Date Completed 16.01.2024 Date Revised 16.01.2024 published: Electronic Citation Status MEDLINE |
---|
doi: |
10.1038/s41467-023-43826-7 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM365567795 |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | NLM365567795 | ||
003 | DE-627 | ||
005 | 20240116231941.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231226s2023 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1038/s41467-023-43826-7 |2 doi | |
028 | 5 | 2 | |a pubmed24n1261.xml |
035 | |a (DE-627)NLM365567795 | ||
035 | |a (NLM)38065962 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Tao, Jing |e verfasserin |4 aut | |
245 | 1 | 0 | |a Excess PrPC inhibits muscle cell differentiation via miRNA-enhanced liquid-liquid phase separation implicated in myopathy |
264 | 1 | |c 2023 | |
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 16.01.2024 | ||
500 | |a Date Revised 16.01.2024 | ||
500 | |a published: Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a © 2023. The Author(s). | ||
520 | |a The cellular prion protein (PrPC) is required for skeletal muscle function. Here, we report that a higher level of PrPC accumulates in the cytoplasm of the skeletal muscle of six myopathy patients compared to controls. PrPC inhibits skeletal muscle cell autophagy, and blocks myoblast differentiation. PrPC selectively binds to a subset of miRNAs during myoblast differentiation, and the colocalization of PrPC and miR-214-3p was observed in the skeletal muscle of six myopathy patients with excessive PrPC. We demonstrate that PrPC is overexpressed in skeletal muscle cells under pathological conditions, inhibits muscle cell differentiation by physically interacting with a subset of miRNAs, and selectively recruits these miRNAs into its phase-separated condensate in living myoblasts, which in turn enhances liquid-liquid phase separation of PrPC, promotes pathological aggregation of PrP, and results in the inhibition of autophagy-related protein 5-dependent autophagy and muscle bundle formation in myopathy patients characterized by incomplete muscle regeneration | ||
650 | 4 | |a Journal Article | |
650 | 7 | |a MicroRNAs |2 NLM | |
650 | 7 | |a MIRN214 microRNA, human |2 NLM | |
650 | 7 | |a PrPC Proteins |2 NLM | |
700 | 1 | |a Zeng, Yanping |e verfasserin |4 aut | |
700 | 1 | |a Dai, Bin |e verfasserin |4 aut | |
700 | 1 | |a Liu, Yin |e verfasserin |4 aut | |
700 | 1 | |a Pan, Xiaohan |e verfasserin |4 aut | |
700 | 1 | |a Wang, Li-Qiang |e verfasserin |4 aut | |
700 | 1 | |a Chen, Jie |e verfasserin |4 aut | |
700 | 1 | |a Zhou, Yu |e verfasserin |4 aut | |
700 | 1 | |a Lu, Zuneng |e verfasserin |4 aut | |
700 | 1 | |a Xie, Liwei |e verfasserin |4 aut | |
700 | 1 | |a Liang, Yi |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Nature communications |d 2010 |g 14(2023), 1 vom: 08. Dez., Seite 8131 |w (DE-627)NLM199274525 |x 2041-1723 |7 nnns |
773 | 1 | 8 | |g volume:14 |g year:2023 |g number:1 |g day:08 |g month:12 |g pages:8131 |
856 | 4 | 0 | |u http://dx.doi.org/10.1038/s41467-023-43826-7 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 14 |j 2023 |e 1 |b 08 |c 12 |h 8131 |