izpis_h1_title_alt

Insulin, dibutyryl-cAMP, and glucose modulate expression of patatin-like domain containing protein 7 in cultured human myotubes
ID Miš, Katarina (Avtor), ID Lulić, Ana-Marija (Avtor), ID Marš, Tomaž (Avtor), ID Pirkmajer, Sergej (Avtor), ID Katalinić, Maja (Avtor)

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Izvleček
Expression of patatin-like phospholipase domain containing protein 7 (PNPLA7), also known as neuropathy target esterase-related esterase (NRE), a lysophospholipase, increases with fasting and decreases with feeding in mouse skeletal muscle, indicating it is regulated by insulin, counterregulatory hormones, such as glucocorticoids and catecholamines, and/or nutrients. In cultured mouse adipocytes insulin reduces Pnpla7 expression, underscoring the possibility that insulin regulates PNPLA7 in skeletal muscle. The first aim of this study was to establish whether PNPLA7 is functionally expressed in cultured human skeletal muscle cells. The second aim was to determine whether PNPLA7 is regulated by insulin, glucocorticoids, cAMP/protein kinase A pathway, and/or glucose. Cultured human skeletal muscle cells expressed PNPLA7 mRNA and protein. Gene silencing of PNPLA7 in myoblasts reduced the phosphorylation of 70 kDa ribosomal protein S6 kinase and ribosomal protein S6 as well as the abundance of α1-subunit of Na$^+$,K$^+$-ATPase and acetyl-CoA carboxylase, indirectly suggesting that PNPLA7 is functionally important. In myotubes, insulin suppressed PNPLA7 mRNA at 1 g/L glucose, but not at low (0.5 g/L) or high (4.5 g/L) concentrations. Treatment with synthetic glucocorticoid dexamethasone and activator of adenylyl cyclase forskolin had no effect on PNPLA7 regardless of glucose concentration, while dibutyryl-cAMP, a cell-permeable cAMP analogue, suppressed PNPLA7 mRNA at 4.5 g/L glucose. The abundance of PNPLA7 protein correlated inversely with the glucose concentrations. Collectively, our results highlight that PNPLA7 in human myotubes is regulated by metabolic signals, implicating a role for PNPLA7 in skeletal muscle energy metabolism.

Jezik:Angleški jezik
Ključne besede:insulin, dexamethasone, dibutyryl-cAMP, PNPLA7, NRE, forskolin, glucose, cultured human myotubes
Vrsta gradiva:Članek v reviji
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:MF - Medicinska fakulteta
Status publikacije:Objavljeno
Različica publikacije:Objavljena publikacija
Leto izida:2023
Št. strani:13 str.
Številčenje:Vol. 14, art. 1139303
PID:20.500.12556/RUL-153983 Povezava se odpre v novem oknu
UDK:616-092
ISSN pri članku:1664-2392
DOI:10.3389/fendo.2023.1139303 Povezava se odpre v novem oknu
COBISS.SI-ID:146622211 Povezava se odpre v novem oknu
Datum objave v RUL:17.01.2024
Število ogledov:834
Število prenosov:36
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Gradivo je del revije

Naslov:Frontiers in endocrinology
Založnik:Frontiers Media
ISSN:1664-2392
COBISS.SI-ID:3340154 Povezava se odpre v novem oknu

Licence

Licenca:CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.

Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:insulin, deksametazon, dibutiril-cAMP

Projekti

Financer:HRZZ - Croatian Science Foundation
Številka projekta:UIP-2017-05-7260
Naslov:Molekularni mehanizmi toksičnosti protuotrova i potencijalnih lijekova

Financer:ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:P3-0043
Naslov:Molekularni mehanizmi razvoja in delovanja skeletne mišice

Financer:ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:J7-3153
Naslov:Molekularni mehanizmi specifičnosti pri uravnavanju izločanja in delovanja citokinov mišičnega izvora

Financer:ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:BI-HR/20-21-041

Financer:HRZZ - Croatian Science Foundation
Program financ.:Bilateral grant

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