Ashok Kujur,
S. John Mary*,
Delinta D,
Ajila A,
Jesuraj P,
Christina C,
Gunasekar C.J,
- Assistant Professor, Department of Chemistry, Loyola College, Sterling Road, Chennai, Tamil Nadu, India
- Assistant Professor, Department of Chemistry, Loyola College, Sterling Road, Chennai, Tamil Nadu, India
- Research Scholar, Loyola Institute of Frontier Energy (LIFE), Loyola College, Sterling Road, Chennai, Tamil Nadu, India
- Research Scholar, Loyola Institute of Frontier Energy (LIFE), Loyola College, Sterling Road, Chennai, Tamil Nadu, India
- Research Scholar, Loyola Institute of Frontier Energy (LIFE), Loyola College, Sterling Road, Chennai, Tamil Nadu, India
- Research Scholar, Loyola Institute of Frontier Energy (LIFE), Loyola College, Sterling Road, Chennai, Tamil Nadu, India
- Assistant Professor, Department of Chemistry, Loyola College, Sterling Road, Chennai, Tamil Nadu, India
Abstract
Background: Pro-inflammatory cytokines, such as TNF-α, IL-1β, IL-6, and IL-8, seem to play a crucial role in the progression of NAFLD as they activate the transcription factor NF-кB. The activated NF-кBp50/RelA subunits are translocated to the nucleus by Importin α3 and Importin α4. Numerous studies have indicated a negative association between NAFLD and vitamin D levels. Low vitamin D levels have been correlated with histological severity, necro-inflammation, and fibrosis in NAFLD. Non-alcoholic fatty liver disease (NAFLD) affects about one-third of the population in the United States and Western countries, reaching up to 90% among obese individuals and those undergoing bariatric surgery. Characterized by hepatic fat accumulation, NAFLD progresses from simple steatosis to non-alcoholic steatohepatitis (NASH), fibrosis, and, in rare cases, hepatocellular carcinoma. Linked intricately with metabolic syndrome, including diabetes and obesity, NAFLD development involves insulin resistance and hyperinsulinemia. Experimental evidence consistently associates low vitamin D levels with NAFLD severity, independent of age, gender, and BMI. Pro-inflammatory cytokines, such as TNF-α and IL-6, play critical roles in NAFLD, with positive correlations between liver fibrosis and TNF-α levels in NASH patients. The inflammatory cascade involves NF-κB activation, Importin α3, and Importin α4. Vitamin D emerges as a key player, up-regulating the NF-κB inhibitor IкBα and reducing pro-inflammatory activity. Studies in NASH models highlight vitamin D’s positive impact on inflammation, fibrosis, and insulin resistance. Recent research underscores calcitriol’s role in decreasing Importin α3 expression, influencing NF-κB translocation. This study provides novel insights into calcitriol’s effects on Importin α3 and IκBα in HepG-2 cells, unraveling cellular and molecular mechanisms in the intricate interplay between vitamin D and NAFLD pathology.
Objective: Vitamin D may resolve the ongoing inflammation observed in NAFLD by reducing the effects of pro-inflammatory cytokines that are extensively produced in NAFLD.
Methods: “HepG-2 cell cultures were subjected to calcitriol stimulation, both in the presence and absence of pro-inflammatory cytokines alongside the anti-inflammatory cytokine IL-10. Quantitative polymerase chain reaction (qPCR) was employed to assess mRNA expression levels of Importin α3 and Importin α3. Additionally, immunofluorescence was utilized for antibody detection.”
Results: Pro-inflammatory cytokines significantly increase the mRNA and protein expression of Importin-α3 in HepG2 cells. Treatment of HepG-2s with calcitriol significantly decreases the mRNA and protein expression of Importin-α3 and attenuates the effects of pro-inflammatory cytokines.
Conclusion: Our data suggest that, under inflammatory conditions, calcitriol plays an inhibitory role in the regulation of NF-кB by decreasing the expression of Importin α3. Thus, calcitriol reduces the translocation of NF-кB and thereby lowers its transcriptional activities.
Keywords: Calcitriol, importin α3, inflammation, NAFLD, pro-inflammatory cytokines, vitamin D
[This article belongs to International Journal of Cheminformatics ]
Ashok Kujur, S. John Mary*, Delinta D, Ajila A, Jesuraj P, Christina C, Gunasekar C.J. Vitamin D Mitigates Inflammation and Downregulates Importin α3 in Non-Alcoholic Fatty Liver Disease (NAFLD). International Journal of Cheminformatics. 2026; 04(01):1-16.
Ashok Kujur, S. John Mary*, Delinta D, Ajila A, Jesuraj P, Christina C, Gunasekar C.J. Vitamin D Mitigates Inflammation and Downregulates Importin α3 in Non-Alcoholic Fatty Liver Disease (NAFLD). International Journal of Cheminformatics. 2026; 04(01):1-16. Available from: https://journals.stmjournals.com/ijci/article=2026/view=242774
References
- Sung KC, Kim SH. Interrelationship between fatty liver and insulin resistance in the development of type 2 diabetes. J Clin Endocrinol Metab. 2011;96(4):1093–1097.
- Boza C, et al. Predictors of non-alcoholic steatohepatitis in obese patients undergoing gastric bypass. Obes Surg. 2005;15(8):1148–1153.
- Tarantino G. Hepatic steatosis, low-grade chronic inflammation and hormone/growth factor/adipokine imbalance. World J Gastroenterol. 2010;16(38):4773–4783.
- Boppidi H. Non-alcoholic fatty liver disease: hepatic manifestation of obesity and the metabolic syndrome. Postgrad Med. 2008;120(2):E01–E07.
- Oh MS, et al. Associations among the degree of non-alcoholic fatty liver disease, metabolic syndrome, degree of obesity in children, and parental obesity. Pediatr Gastroenterol Hepatol Nutr. 2016;19(3):199–206.
- Targher G, et al. Associations between serum 25-hydroxyvitamin D3 concentrations and liver histology in patients with non-alcoholic fatty liver disease. Nutr Metab Cardiovasc Dis. 2007;17(7):517–524.
- Younossi ZM, et al. Changes in the prevalence of the most common causes of chronic liver diseases in the United States from 1988 to 2008. Clin Gastroenterol Hepatol. 2011;9(6):524–530.e1.
- Manco M, Ciampalini P, Nobili V. Low levels of 25-hydroxyvitamin D3 in children with biopsy-proven non-alcoholic fatty liver disease. Hepatology. 2010;51(6):2229.
- Alkhouri N, et al. The inflamed liver and atherosclerosis: a link between histologic severity of non-alcoholic fatty liver disease and increased cardiovascular risk. Dig Dis Sci. 2010;55(9):2644–2650.
- Day CP. Non-alcoholic fatty liver disease: a massive problem. Clin Med (Lond). 2011;11(2):176–178.
- Hotamisligil GS, Shargill NS, Spiegelman BM. Adipose expression of tumor necrosis factor-α: direct role in obesity-linked insulin resistance. Science. 1993;259(5091):87–91.
- Xu A, et al. The fat-derived hormone adiponectin alleviates alcoholic and non-alcoholic fatty liver diseases in mice. J Clin Invest. 2003;112(1):91–100.
- Stienstra R, et al. Kupffer cells promote hepatic steatosis via interleukin-1β-dependent suppression of peroxisome proliferator-activated receptor α activity. Hepatology. 2010;51(2):511–522.
- Subramaniyan V, Lubau NSA, Mukerjee N, Kumarasamy V. Alcohol-induced liver injury in signalling pathways and curcumin’s therapeutic potential. Toxicol Rep. 2023;11:355–367.
- Agrawal T, Gupta GK, Agrawal DK. Calcitriol decreases expression of importin α3 and attenuates RelA translocation in human bronchial smooth muscle cells. J Clin Immunol. 2012;32(5):1093–1103.
- Alexander MR, Murgai M, Moehle CW, Owens GK. Interleukin-1β modulates smooth muscle cell phenotype to a distinct inflammatory state relative to PDGF-DD via NF-κB-dependent mechanisms. Physiol Genomics. 2012;44(7):417–429.
- Cohen-Lahav M, Shany S, Tobvin D, Chaimovitz C, Douvdevani A. Vitamin D decreases NF-κB activity by increasing IκBα levels. Nephrol Dial Transplant. 2006;21(4):889–897.
- Fagerlund R, Melén K, Cao X, Julkunen I. NF-κB p52, RelB and c-Rel are transported into the nucleus via a subset of importin α molecules. Cell Signal. 2008;20(8):1442–1451.
- Moore KW, de Waal Malefyt R, Coffman RL, O’Garra A. Interleukin-10 and the interleukin-10 receptor. Annu Rev Immunol. 2001;19:683–765.
- Dhingra S, Sharma AK, Arora RC, Slezak J, Singal PK. IL-10 attenuates TNF-α-induced NF-κB pathway activation and cardiomyocyte apoptosis. Cardiovasc Res. 2009;82(1):59–66.
- Beppu LY, et al. Tregs facilitate obesity and insulin resistance via a Blimp-1/IL-10 axis. JCI Insight. 2021;6(5):e140644.
- Fontes-Cal TCM, et al. Crosstalk between plasma cytokines, inflammation, and liver damage as a new strategy to monitoring NAFLD progression. Front Immunol. 2021;12:708959.
- Gwechenberger M, et al. Cardiac myocytes produce interleukin-6 in culture and in viable border zone of reperfused infarctions. Circulation. 1999;99(4):546–551.
- Kishimoto T. IL-6: from its discovery to clinical applications. Int Immunol. 2010;22(5):347–352.
- Ridker PM, Rifai N, Stampfer MJ, Hennekens CH. Plasma concentration of interleukin-6 and the risk of future myocardial infarction among apparently healthy men. Circulation. 2000;101(15):1767–1772.
- Spranger J, et al. Inflammatory cytokines and the risk to develop type 2 diabetes. Diabetes. 2003;52(3):812–817.
- Ueki K, Kondo T, Kahn CR. Suppressor of cytokine signaling 1 and 3 cause insulin resistance through inhibition of tyrosine phosphorylation of insulin receptor substrate proteins. Mol Cell Biol. 2004;24(12):5434–5446.
- Bickel M. The role of interleukin-8 in inflammation and mechanisms of regulation. J Periodontol. 1993;64(5 Suppl):456–460.
- Bahcecioglu IH, et al. Levels of serum hyaluronic acid, TNF-α and IL-8 in patients with non-alcoholic steatohepatitis. Hepatogastroenterology. 2005;52(65):1549–1553.
- Torer N, Ozenirler S, Yucel A, Bukan N, Erdem O. Importance of cytokines, oxidative stress and expression of BCL-2 in the pathogenesis of non-alcoholic steatohepatitis. Scand J Gastroenterol. 2007;42(9):1095–1101.
- Seo YY, et al. Tumor necrosis factor-α as a predictor for the development of non-alcoholic fatty liver disease: a 4-year follow-up study. Endocrinol Metab (Seoul). 2013;28(1):41–45.
- Duan Y, et al. Association of inflammatory cytokines with non-alcoholic fatty liver disease. Front Immunol. 2022;13:880298.
- Gupta SC, Sundaram C, Reuter S, Aggarwal BB. Inhibiting NF-κB activation by small molecules as a therapeutic strategy. Biochim Biophys Acta. 2010;1799(10–12):775–787.
- Janjetovic Z, et al. 20-Hydroxycholecalciferol decreases NF-κB activity by increasing IκBα levels in human keratinocytes. PLoS One. 2009;4(4):e5988.
- Ebert R, et al. Down-regulation by nuclear factor κB of human 25-hydroxyvitamin D3 1α-hydroxylase promoter. Mol Endocrinol. 2004;18(10):2440–2450.
- Tse AKW, et al. 1,25-Dihydroxyvitamin D3 induces biphasic NF-κB responses during HL-60 leukaemia cell differentiation. Exp Cell Res. 2007;313(8):1722–1734.
- Zhuo Y, et al. African swine fever virus MGF360-12L inhibits type I interferon production by blocking importin α–NF-κB signaling. Virol Sin. 2021;36(2):176–186.
- Diaz C, Thankam FG, Agrawal DK. Karyopherins in the remodelling of extracellular matrix: implications in tendon injury. J Orthop Sports Med. 2023;5:1–12.
| Volume | 04 |
| Issue | 01 |
| Received | 22/01/2026 |
| Accepted | 19/02/2026 |
| Published | 28/02/2026 |
| Publication Time | 37 Days |
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