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Arginine depletion attenuates renal cystogenesis in tuberous sclerosis complex model.


ABSTRACT: Cystic kidney disease is a leading cause of morbidity in patients with tuberous sclerosis complex (TSC). We characterize the misregulated metabolic pathways using cell lines, a TSC mouse model, and human kidney sections. Our study reveals a substantial perturbation in the arginine biosynthesis pathway in TSC models with overexpression of argininosuccinate synthetase 1 (ASS1). The rise in ASS1 expression is dependent on the mechanistic target of rapamycin complex 1 (mTORC1) activity. Arginine depletion prevents mTORC1 hyperactivation and cell cycle progression and averts cystogenic signaling overexpression of c-Myc and P65. Accordingly, an arginine-depleted diet substantially reduces the TSC cystic load in mice, indicating the potential therapeutic effects of arginine deprivation for the treatment of TSC-associated kidney disease.

SUBMITTER: Amleh A 

PROVIDER: S-EPMC10313931 | biostudies-literature | 2023 Jun

REPOSITORIES: biostudies-literature

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Arginine depletion attenuates renal cystogenesis in tuberous sclerosis complex model.

Amleh Athar A   Chen Hadass Pri HP   Watad Lana L   Abramovich Ifat I   Agranovich Bella B   Gottlieb Eyal E   Ben-Dov Iddo Z IZ   Nechama Morris M   Volovelsky Oded O  

Cell reports. Medicine 20230607 6


Cystic kidney disease is a leading cause of morbidity in patients with tuberous sclerosis complex (TSC). We characterize the misregulated metabolic pathways using cell lines, a TSC mouse model, and human kidney sections. Our study reveals a substantial perturbation in the arginine biosynthesis pathway in TSC models with overexpression of argininosuccinate synthetase 1 (ASS1). The rise in ASS1 expression is dependent on the mechanistic target of rapamycin complex 1 (mTORC1) activity. Arginine dep  ...[more]

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