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The Role of MAPRE2 and Microtubules in Maintaining Normal Ventricular Conduction

Authors :
Chiang, DY
Verkerk, AO
Victorio, R
Shneyer, BI
van der Vaart, B
Jouni, M
Narendran, N
Kc, A
Sampognaro, JR
Vetrano-Olsen, F
Oh, JS
Buys, E
de Jonge, B
Shah, DA
Kiviniemi, T
Burridge, PW
Bezzina, CR
Akhmanova, A
Macrae, CA
Chiang, DY
Verkerk, AO
Victorio, R
Shneyer, BI
van der Vaart, B
Jouni, M
Narendran, N
Kc, A
Sampognaro, JR
Vetrano-Olsen, F
Oh, JS
Buys, E
de Jonge, B
Shah, DA
Kiviniemi, T
Burridge, PW
Bezzina, CR
Akhmanova, A
Macrae, CA
Source :
Circulation Research vol.134 (2024) date: 2024-01-04 nr.1 p.46-59 [ISSN 0009-7330]
Publication Year :
2024

Abstract

BACKGROUND: Brugada syndrome is associated with loss-of-function SCN5A variants, yet these account for only ≈20% of cases. A recent genome-wide association study identified a novel locus within MAPRE2, which encodes EB2 (microtubule end-binding protein 2), implicating microtubule involvement in Brugada syndrome. METHODS: A mapre2 knockout zebrafish model was generated using CRISPR/Cas9 (clustered regularly interspaced short palindromic repeats/clustered regularly interspaced short palindromic repeat–associated protein 9) and validated by Western blot. Larval hearts at 5 days post-fertilization were isolated for voltage mapping and immunocytochemistry. Adult fish hearts were used for ECG, patch clamping, and immunocytochemistry. Morpholinos were injected into embryos at 1-cell stage for knockdown experiments. A transgenic zebrafish line with cdh2 tandem fluorescent timer was used to study adherens junctions. Microtubule plus-end tracking and patch clamping were performed in human induced pluripotent stem cell derived cardiomyocytes (iPSC-CMs) with MAPRE2 knockdown and knockout, respectively. RESULTS: Voltage mapping of mapre2 knockout hearts showed a decrease in ventricular maximum upstroke velocity of the action potential and conduction velocity, suggesting loss of cardiac voltage-gated sodium channel function. ECG showed QRS prolongation in adult knockout fish, and patch clamping showed decreased sodium current density in knockout ventricular myocytes and arrhythmias in knockout iPSC-CMs. Confocal imaging showed disorganized adherens junctions and mislocalization of mature Ncad (N-cadherin) with mapre2 loss of function, associated with a decrease of detyrosinated tubulin. MAPRE2 knockdown in iPSC-CMs led to an increase in microtubule growth velocity and distance, indicating changes in microtubule dynamics. Finally, knockdown of ttl encoding tubulin tyrosine ligase in mapre2 knockout larvae rescued tubulin detyrosination and ventricular

Details

Database :
OAIster
Journal :
Circulation Research vol.134 (2024) date: 2024-01-04 nr.1 p.46-59 [ISSN 0009-7330]
Notes :
DOI: 10.1161/CIRCRESAHA.123.323231, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1445835465
Document Type :
Electronic Resource