Journal of Immunology Research

Journal of Immunology Research / 2020 / Article

Research Article | Open Access

Volume 2020 |Article ID 9484015 |

Magdalena Zurawek, Marta Fichna, Piotr Fichna, Maria Czainska, Natalia Rozwadowska, "Upregulation of FOXO3 in New-Onset Type 1 Diabetes Mellitus", Journal of Immunology Research, vol. 2020, Article ID 9484015, 4 pages, 2020.

Upregulation of FOXO3 in New-Onset Type 1 Diabetes Mellitus

Academic Editor: Cinzia Ciccacci
Received10 Mar 2020
Accepted22 Jul 2020
Published12 Aug 2020


Forkhead box O (FOXO) transcription factors have been implicated in the development and differentiation of the immune cells. FOXO3 plays a crucial role in physiologic and pathologic immune response. FOXO3, cooperatively with FOXO1, control the development and function of Foxp3+ regulatory T cells (Treg). Since the lack of Treg-mediated control has fundamental impact on type 1 diabetes mellitus (T1DM) development, we investigated FOXO3 expression in patients with T1DM. FOXO3 expression was estimated in peripheral blood mononuclear cells (PBMCs) from newly diagnosed T1DM pediatric patients () and age-matched healthy donors () by reahavel-time PCR and TaqMan gene expression assays. Expression analysis revealed significant upregulation of FOXO3 in T1DM (). Stratification of the T1DM group according to the presence of initial diabetic ketoacidosis (DKA) did not indicate differences in FOXO3 expression in patients with DKA compared to a mild T1DM onset (). In conclusion, overexpression of FOXO3 is correlated with the ongoing islet autoimmune destruction and might suggest a potential role for this gene in the pathogenesis of type 1 diabetes mellitus.

1. Introduction

FOXO3 (forkhead box O3) protein belongs to the family of transcription factors included withal FOXO1, FOXO4, and FOXO6. FOXO3 is regulated via the phosphoinositide 3-kinase (PI3K)/serine/threonine-specific kinase (Akt) signaling pathway [1]. The active, nonphosphorylated FOXO3 form is localized in the nucleus and regulates gene transcription. Phosphorylation of FOXO3 in the PI3K/Akt pathway results in its exclusion from the nucleus and termination of transcriptional activity [2]. FOXO3 has been implicated in the regulation of diverse biological processes, including cell survival, proliferation, and apoptosis [3]. FOXO3 is expressed in immune cells, and recently, there has been a surge in interest to investigate the importance of FOXO3 in lymphoid homeostasis [46]. Upregulation of FOXO3 was observed in polymorphonuclear cells and peripheral blood mononuclear cells from patients with rheumatoid arthritis [7]. Overexpression of FOXO3 is mediated by T cell receptor stimulation [8]. In consequence, FOXO3 promotes polarization of CD4+ T cells towards the pathogenic T helper cells producing interferon γ and granulocyte monocyte colony-stimulating factor. FOXO3-/- mice exhibit reduced susceptibility to experimental autoimmune encephalomyelitis [8].

In this study, we investigate the expression level of FOXO3 in PBMCs from newly diagnosed type 1 diabetes mellitus pediatric patients. Upregulation of FOXO3 was observed in the T1DM group compared to the age-matched healthy controls—a finding that might suggest a potential role of this gene in autoimmunity.

2. Study Groups

The qRT-PCR of FOXO3 gene was conducted in 28 newly diagnosed T1DM subjects ( years, 4 females (14%), 24 males (86%)) and 27 age-matched healthy donors ( years, 13 (48%) females, 14 (52%) males). Patients were recruited at the Department of Paediatric Diabetes and Obesity, Poznan University of Medical Sciences. The diagnosis of diabetes was based upon the WHO criteria. Autoimmune origin of the disease was confirmed by positive serum autoantibodies to insulin (IAA) and/or glutamic acid decarboxylase (GADA) and/or islet antigen-2 (IA-2A). Clinical characterization of patients is summarized in Table 1. Pediatric control individuals with negative personal and family history of autoimmunity and no clinical signs of the autoimmune disorders were obtained from an outpatient pediatric practice in the course of routine screening. Only subjects with no clinical symptoms of hyperglycemia and fasting blood glucose within the reference range (≤5.5 mmol/l) were included in the control group.

Clinical featuresT1DSevere T1D onsetMild T1D onset
(%) (%) (%)

Gender, F/M4/24
Age (y)
BMI (kg/m2)
HbA1c (%)
C peptide (nmol/l)
25-OH-D (ng/ml)
DKA12 (43)12 (100)16 (0)
IAA7 (25)3 (25)4 (25)
GADA21 (75)9 (75)12 (75)
IA2A23 (82)11 (92)12 (75)

BMI: body mass index; HbA1c: glycated haemoglobin A1c; 25-OH-D: 25-hydroxyvitamin D; DKA: diabetic ketoacidosis; IAA: antibodies to insulin; GADA: antibodies to glutamic acid decarboxylase; IA2A: antibodies to islet antigen-2; clinical features presented as ; number of subjects (%); , values estimated by unpaired -test, severe T1D onset vs. mild T1D onset subgroup.

3. Methods

3.1. FOXO3 Expression Analysis

FOXO3 expression was assessed in PBMCs isolated from the peripheral blood (4 ml for each subject) by density gradient centrifugation in Histopaque-1077 (Sigma Aldrich, Germany). Total RNA was extracted with a TRI Reagent (Sigma Aldrich, Germany) following the manufacturer’s protocol. The equal amount of RNA (500 ng per sample) was converted to cDNA using a QuantiTect Reverse Transcription Kit (QIAGEN, Germany). A quantitative real-time PCR using an aliquot of cDNA equivalent of 5 ng total RNA, TaqMan gene expression assay (Applied Biosystems, Thermo Fisher Scientific, USA), and HOT FIREPol Probe Universal qPCR Mix (Solis BioDyne, Estonia) was performed in a total volume of 15 μl on a BioRad CFX96 Real-Time PCR instrument (BioRad Laboratories, CA, USA). All reactions were run in triplicate. The expression level of FOXO3 (assay ID Hs00818121_m1) was normalized to beta-2 microglobulin housekeeping gene (assay ID Hs00984230_m1). Mean cycle threshold (Ct) values were estimated with BioRad CFX Manager 3.1 software. Relative expression levels were calculated using the 2ΔCt formula. Statistical analysis was performed using GraphPad Prism 5 (GraphPad Software Inc., CA, USA). Statistical significance of the differences between relative expression levels was determined with an unpaired -test. values < 0.05 were considered statistically significant.

4. Results and Discussion

Type 1 diabetes mellitus is an autoimmune disorder that results from the lack of endogenous insulin secretion from the pancreatic beta cells. Although T-mediated destruction of beta cells is observed, the precise etiology and pathological mechanisms are still poorly understood. Genetic predisposition and environmental factors contribute to the development of type 1 diabetes mellitus [9]. HLA locus, specifically the haplotypes DRB103-DQA105-DQB102 (DR3-DQ2) and DRB104-DQA103-DQB103:02 (DR4-DQ8) are major genetic risk factors [10]. To date, around 60 non-HLA T1DM susceptibility loci have been identified, mostly related to immune response, for instance, genes encoding lymphocyte protein tyrosine phosphatase (PTPN22), cytotoxic T-lymphocyte protein 4 (CTLA4), subunit alpha of the interleukin-2 receptor (IL2RA), and interferon-induced helicase C domain-containing protein 1 (IFIH1) [1113].

Our previous study indicated FOXO3 as a potential target for miR-487a-3p, which is upregulated in T1DM [14]. These results prompted us to investigate the FOXO3 expression in type 1 diabetes mellitus patients. In order to reduce the interference of the initial metabolic status, PBMCs were collected from patients with normalized ketonaemia and glycemia and fully rehydrated. In addition, T1DM patients and control subjects included in the study did not present infection symptoms, confirmed by negative inflammatory tests (complete blood count, C-reactive protein tests). The type 1 diabetes mellitus group was further stratified according to the presence or absence of diabetic ketoacidosis (DKA) at initial presentation, which reflects severe and moderate disease onsets, respectively. Expression analysis revealed significant upregulation of FOXO3 in the new-onset T1DM group compared to the age-matched healthy controls (Figure 1). However, we did not observe statistically significant differences in FOXO3 expression in patients with DKA compared to the mild T1DM onset group (Figure 1). Consequently, FOXO3 expression is correlated with the ongoing autoimmune islet destruction, although not with the severity of the autoimmune process. A current study failed to confirm the previous global expression analysis of PBMCs from children with newly diagnosed type 1 diabetes mellitus (GEO DataSets, Accession GDS3875) [15]. The microarray analysis did not reveal dysregulation of FOXO3 in the group of T1DM patients at one month and at four months after diagnosis [15].

Based on our previous study, we hypothesized that overexpression of miR-487a-3p in T1DM might result in downregulation of FOXO3 and hence affect the immune function. Current results imply that FOXO3 is apparently not regulated via miR-487a-3p; however, additional in vitro study is needed to explore the manner of FOXO3 regulation. Yang et al. have demonstrated the mechanisms protecting FOXO3 from being targeted by certain miRNAs [16]. The Foxo3 pseudogene (Foxo3P) and the Foxo3 circular RNA (circ-Foxo3) act as a sponge and bind several miRNAs, including miR-22, miR-136, miR-138, miR-149, miR-433, miR-762, miR-3614-5p, and miR-3622b-5p. Subsequently, Foxo3P and circ-Foxo3 ensure FOXO3 gene expression and protein activity.

5. Conclusion

Overexpression of FOXO3 in type 1 diabetes mellitus might suggest a potential role of this gene in the development of autoimmune disease. Further in vitro and ex vivo functional studies will address the issue of FOXO3 contribution to immune tolerance dysregulation.

Data Availability

Data presented in the manuscript are available upon request from corresponding author Magdalena Zurawek,

Ethical Approval

The study was approved by the local Ethics Committee at the Poznan University of Medical Sciences (decision No. 656/15), and all procedures were in accordance with the Declaration of Helsinki.

Informed consent was obtained from the parents/legal representatives of the minor patients.

Conflicts of Interest

The authors declare that they have no conflict of interests.

Authors’ Contributions

MZ designed the study, performed experiments, analyzed data, and wrote the manuscript, MF and PF collected T1DM patients’ samples and clinical data, MC collected control subjects’ samples, and NR revised the manuscript.


The study was supported by the Polish Diabetes Association, Artur Czyzyk Research Grant 2015.


  1. K. U. Birkenkamp and P. J. Coffer, “FOXO transcription factors as regulators of immune homeostasis: molecules to die for?” Journal of Immunology, vol. 171, no. 4, pp. 1623–1629, 2003. View at: Publisher Site | Google Scholar
  2. A. Brunet, A. Bonni, M. J. Zigmond et al., “Akt promotes cell survival by phosphorylating and inhibiting a Forkhead transcription factor,” Cell, vol. 96, no. 6, pp. 857–868, 1999. View at: Publisher Site | Google Scholar
  3. H. Tran, A. Brunet, E. C. Griffith, and M. E. Greenberg, “The many forks in FOXO's road,” Science Signaling, vol. 2003, no. 172, p. re5, 2003. View at: Publisher Site | Google Scholar
  4. A. S. Dejean, D. R. Beisner, I. L. Ch'en et al., “Transcription factor Foxo3 controls the magnitude of T cell immune responses by modulating the function of dendritic cells,” Nature immunology, vol. 10, no. 5, pp. 504–513, 2009. View at: Publisher Site | Google Scholar
  5. Y. M. Kerdiles, E. L. Stone, D. L. Beisner et al., “Foxo transcription factors control regulatory T cell development and function,” Immunity, vol. 33, no. 6, pp. 890–904, 2010. View at: Publisher Site | Google Scholar
  6. J. A. Sullivan, E. H. Kim, E. H. Plisch, S. L. Peng, and M. Suresh, “FOXO3 regulates CD8 T cell memory by T cell-intrinsic mechanisms,” PLoS pathogens, vol. 8, no. 2, 2012. View at: Publisher Site | Google Scholar
  7. F. Turrel-Davin, A. Tournadre, A. Pachot et al., “FoxO3a involved in neutrophil and T cell survival is overexpressed in rheumatoid blood and synovial tissue,” Annals of the rheumatic diseases, vol. 69, no. 4, pp. 755–760, 2010. View at: Publisher Site | Google Scholar
  8. C. Stienne, M. F. Michieletto, M. Benamar et al., “Foxo3 transcription factor drives pathogenic T helper 1 differentiation by inducing the expression of Eomes,” Immunity, vol. 45, no. 4, pp. 774–787, 2016. View at: Publisher Site | Google Scholar
  9. J. A. Bluestone, K. Herold, and G. Eisenbarth, “Genetics, pathogenesis and clinical interventions in type 1 diabetes,” Nature, vol. 464, no. 7293, pp. 1293–1300, 2010. View at: Publisher Site | Google Scholar
  10. H. Erlich, A. M. Valdes, J. Noble et al., “HLA DR-DQ haplotypes and genotypes and type 1 diabetes risk: analysis of the type 1 diabetes genetics consortium families,” Diabetes, vol. 57, no. 4, pp. 1084–1092, 2008. View at: Publisher Site | Google Scholar
  11. N. Bottini, L. Musumeci, A. Alonso et al., “A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes,” Nature genetics, vol. 36, no. 4, pp. 337-338, 2004. View at: Publisher Site | Google Scholar
  12. D. J. Smyth, V. Plagnol, N. M. Walker et al., “Shared and distinct genetic variants in type 1 diabetes and celiac disease,” The New England journal of medicine, vol. 359, no. 26, pp. 2767–2777, 2008. View at: Publisher Site | Google Scholar
  13. H. Ueda, J. M. M. Howson, L. Esposito et al., “Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease,” Nature, vol. 423, no. 6939, pp. 506–511, 2003. View at: Publisher Site | Google Scholar
  14. M. Zurawek, A. Dzikiewicz-Krawczyk, K. Izykowska et al., “miR-487a-3p upregulated in type 1 diabetes targets CTLA4 and FOXO3,” Diabetes research and clinical practice, vol. 142, pp. 146–153, 2018. View at: Publisher Site | Google Scholar
  15. E. C. Kaizer, C. L. Glaser, D. Chaussabel, J. Banchereau, and V. Pascual, “Gene expression in peripheral blood mononuclear cells from children with diabetes,” The Journal of clinical endocrinology and metabolism, vol. 92, no. 9, pp. 3705–3711, 2007. View at: Publisher Site | Google Scholar
  16. W. Yang, W. W. Du, X. Li, A. J. Yee, and B. B. Yang, “Foxo3 activity promoted by non-coding effects of circular RNA and Foxo3 pseudogene in the inhibition of tumor growth and angiogenesis,” Oncogene, vol. 35, no. 30, pp. 3919–3931, 2016. View at: Publisher Site | Google Scholar

Copyright © 2020 Magdalena Zurawek et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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