{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"institution":[{"name":"bioRxiv"}],"indexed":{"date-parts":[[2026,10,23]],"date-time":"2026-10-23T21:20:23Z","timestamp":1792790423671,"version":"4.5.0"},"posted":{"date-parts":[[2026,9,23]]},"group-title":"Molecular Biology","reference-count":69,"publisher":"openRxiv","license":[{"start":{"date-parts":[[2026,9,23]],"date-time":"2026-09-23T00:00:00Z","timestamp":1790121600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"funder":[{"award":["BI01BX001000"],"award-info":[{"award-number":["BI01BX001000"]}],"id":[{"id":"https:\/\/ror.org\/05rsv9s98","id-type":"ROR","asserted-by":"publisher"}]},{"name":"Dialysis Clinic, Inc.","award":["C-4149"],"award-info":[{"award-number":["C-4149"]}],"id":[{"id":"https:\/\/ror.org\/058c2a318","id-type":"ROR","asserted-by":"crossref"}]},{"award":["TS240031"],"award-info":[{"award-number":["TS240031"]}],"id":[{"id":"https:\/\/ror.org\/0447fe631","id-type":"ROR","asserted-by":"publisher"}]},{"award":["NHLBIT32HL007736"],"award-info":[{"award-number":["NHLBIT32HL007736"]}],"id":[{"id":"https:\/\/ror.org\/01cwqze88","id-type":"ROR","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"accepted":{"date-parts":[[2026,9,23]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                <jats:sec>\n                  <jats:title>Background<\/jats:title>\n                  <jats:p>\n                    Tuberous Sclerosis Complex (TSC) is caused by inactivating mutations in either the\n                    <jats:italic>TSC1<\/jats:italic>\n                    or\n                    <jats:italic>TSC2<\/jats:italic>\n                    genes, leading to activation of the mammalian target of rapamycin complex 1 (mTORC1) and unhindered cell growth and proliferation. The epithelium of TSC renal cysts in both mice and humans is composed of proliferating A-intercalated (A-IC) cells. The exact molecular mechanism of kidney cystogenesis in TSC remains speculative.\n                  <\/jats:p>\n                <\/jats:sec>\n                <jats:sec>\n                  <jats:title>Hypothesis<\/jats:title>\n                  <jats:p>Superfluous cell proliferation driven by mTORC1 activation increases metabolic demand, causing oxidative stress and excess reactive oxygen species. If unchecked, this overwhelms antioxidant defenses and causes cell death. In TSC kidney cystogenesis, Nuclear Factor Erythroid 2-Related Factor 2 (NFE2L2), also known as NRF2, serves as the \u201cmaster regulator\u201d of antioxidant and anti-inflammatory responses, enabling cells to survive and proliferate by clearing the toxic environment and supplying nutrients and fuel.<\/jats:p>\n                <\/jats:sec>\n                <jats:sec>\n                  <jats:title>Results<\/jats:title>\n                  <jats:p>\n                    RNA-seq and proteomics, along with western blot analysis, showed robust downregulation of Fumarate Hydrase 1 (FH1) and upregulation of NRF2, STAT3, and HIF1\u03b1 in kidneys from TSC mice with moderate or heavy cyst burden. Confocal microscopy and immunohistochemical staining on kidney sections, and\/or western blot studies on nuclear and cytoplasmic fractions, showed nuclear localization of NRF2, STAT3, and HIF1\u03b1. In cyst-lining cells in TSC mouse models, FH1 downregulation was associated with inactivating succination of KEAP1 in immunoprecipitation experiments, promoting NRF2 nuclear localization in A-IC cells lining the cysts. NRF2 nuclear localization was associated with ectopic induction of the glutamine transporter SLC38A3 (SNAT3) on the basolateral membrane and activation of the NH\n                    <jats:sub>3<\/jats:sub>\n                    \/NH\n                    <jats:sub>4<\/jats:sub>\n                    <jats:sup>+<\/jats:sup>\n                    transporters RHCG and RHBG in A-IC cells lining the cysts. Twenty-four h urine NH\n                    <jats:sub>3<\/jats:sub>\n                    \/NH\n                    <jats:sub>4<\/jats:sub>\n                    <jats:sup>+<\/jats:sup>\n                    excretion rates increased significantly in\n                    <jats:italic>Tsc1<\/jats:italic>\n                    KO vs. WT mice.\n                  <\/jats:p>\n                  <jats:p>\n                    The activation of NRF2, STAT3, and HIF1\u03b1 can drive metabolic reprogramming and activate survival genes in proliferating cells. Together with SLC38A3 induction and upregulation of other glutamine and NH\n                    <jats:sub>3<\/jats:sub>\n                    \/NH\n                    <jats:sup>+<\/jats:sup>\n                    transporters, these factors activate glutaminolysis and aerobic glycolysis, supplying nutrients to proliferating cystic epithelial cells and supporting cyst expansion in TSC. Consistent with this central role for glutaminolysis in kidney cystic epithelium and TSC cystogenesis, we find a significant reduction in kidney cyst burden in\n                    <jats:italic>Tsc1<\/jats:italic>\n                    KO mice on a glutamine-free diet.\n                  <\/jats:p>\n                <\/jats:sec>\n                <jats:sec>\n                  <jats:title>Conclusions<\/jats:title>\n                  <jats:p>NRF2 plays a critical role in antioxidant defense. Along with STAT3 and HIF1\u03b1, NRF2 is a key player in metabolic reprogramming through glutaminolysis, which supplies nutrients to proliferating cystic epithelial cells and supports cyst expansion in TSC. These findings suggest that inhibiting or inactivating NRF2, alone or in combination with HIF1\u03b1 or STAT3, may represent a potential treatment strategy for kidney lesions in TSC<\/jats:p>\n                <\/jats:sec>","DOI":"10.64898\/2026.09.22.753536","type":"posted-content","created":{"date-parts":[[2026,9,23]],"date-time":"2026-09-23T15:45:11Z","timestamp":1790178311000},"source":"Crossref","is-referenced-by-count":0,"title":["The Activation of the Transcription Factor NRF2 in Epithelial Cells Lining the Kidney Cysts in Tuberous Sclerosis Complex (TSC): The Interplay of Fumarate Hydratase 1, KEAP1, and NRF2 in Kidney Cystogenesis"],"prefix":"10.64898","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-5710-292X","authenticated-orcid":false,"given":"Sharon","family":"Barone","sequence":"first","affiliation":[{"name":"Department of Medicine, University of New Mexico School of Medicine; Albuquerque, NM"},{"name":"Research Services, New Mexico Veterans Health Care System, 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