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Hypoxia-induced miR-1260b regulates vascular smooth muscle cell proliferation by targeting GDF11

  • Seong, Minhyeong (Division of Life Sciences, College of Life Sciences and Bioengineering, Incheon National University) ;
  • Kang, Hara (Division of Life Sciences, College of Life Sciences and Bioengineering, Incheon National University)
  • Received : 2019.05.08
  • Accepted : 2019.08.30
  • Published : 2020.04.30

Abstract

Vascular smooth muscle cells (VSMCs) are a unique cell type that has unusual plasticity controlled by environmental stimuli. As an abnormal increase of VSMC proliferation is associated with various vascular diseases, tight regulation of VSMC phenotypes is essential for maintaining vascular homeostasis. Hypoxia is one environmental stress that stimulates VSMC proliferation. Emerging evidence has indicated that microRNAs (miRNAs) are critical regulators in the hypoxic responses of VSMCs. Therefore, we previously investigated miRNAs modulated by hypoxia in VSMCs and found that miR-1260b is one of the most upregulated miRNAs under hypoxia. However, the mechanism that underlies the regulation of VSMCs via miR-1260b in response to hypoxia has not been explored. Here we demonstrated that hypoxia-induced miR-1260b promotes VSMC proliferation. We also identified growth differentiation factor 11 (GDF11), a member of the TGF-β superfamily, as a novel target of miR-1260b. miR-1260b directly targets the 3'UTR of GDF11. Downregulation of GDF11 inhibited Smad signaling and consequently enhanced the proliferation of VSMCs. Our findings suggest that miR-1260b-mediated GDF11-Smad-dependent signaling is an essential regulatory mechanism in the proliferation of VSMCs, and this axis is modulated by hypoxia to promote abnormal VSMC proliferation. Therefore, our study unveils a novel function of miR-1260b in the pathological proliferation of VSMCs under hypoxia.

Keywords

References

  1. Owens GK, Kumar MS and Wamhoff BR (2004) Molecular regulation of vascular smooth muscle cell differentiation in development and disease. Physiol Rev 84, 767-801 https://doi.org/10.1152/physrev.00041.2003
  2. Owens GK (1995) Regulation of differentiation of vascular smooth muscle cells. Physiol Rev 75, 487-517 https://doi.org/10.1152/physrev.1995.75.3.487
  3. Lagna G, Ku MM, Nguyen PH, Neuman NA, Davis BN and Hata A (2007) Control of phenotypic plasticity of smooth muscle cells by bone morphogenetic protein signaling through the myocardin-related transcription factors. J Biol Chem 282, 37244-37255 https://doi.org/10.1074/jbc.M708137200
  4. ten Dijke P and Arthur HM (2007) Extracellular control of TGFbeta signalling in vascular development and disease. Nature reviews. Mol Cell Biol 8, 857-869
  5. Semenza GL (2007) Life with oxygen. Science 318, 62-64 https://doi.org/10.1126/science.1147949
  6. Stenmark KR, Fagan KA and Frid MG (2006) Hypoxiainduced pulmonary vascular remodeling: cellular and molecular mechanisms. Circ Res 99, 675-691 https://doi.org/10.1161/01.RES.0000243584.45145.3f
  7. Semenza GL (2012) Hypoxia-inducible factors in physiology and medicine. Cell 148, 399-408 https://doi.org/10.1016/j.cell.2012.01.021
  8. Wang GL, Jiang BH, Rue EA and Semenza GL (1995) Hypoxia-inducible factor 1 is a basic-helix-loop-helix-PAS heterodimer regulated by cellular O2 tension. Proc Natl Acad Sci U S A 92, 5510-5514 https://doi.org/10.1073/pnas.92.12.5510
  9. Ivan M, Harris AL, Martelli F and Kulshreshtha R (2008) Hypoxia response and microRNAs: no longer two separate worlds. J Cell Mol Med 12, 1426-1431 https://doi.org/10.1111/j.1582-4934.2008.00398.x
  10. Kang H and Hata A (2012) MicroRNA regulation of smooth muscle gene expression and phenotype. Curr Opi Hemato 19, 224-231 https://doi.org/10.1097/MOH.0b013e3283523e57
  11. Lee J, Heo J and Kang H (2018) miR-92b-3p-TSC1 axis is critical for mTOR signaling-mediated vascular smooth muscle cell proliferation induced by hypoxia. Cell Death Differ 26, 1782-1795
  12. Hirata H, Ueno K, Nakajima K et al (2013) Genistein downregulates onco-miR-1260b and inhibits Wnt-signalling in renal cancer cells. Br J Can 108, 2070-2078 https://doi.org/10.1038/bjc.2013.173
  13. Li X, Song H, Liu Z and Bi Y (2018) miR-1260b promotes cell migration and invasion of hepatocellular carcinoma by targeting the regulator of G-protein signaling 22. Biotech Lett 40, 57-62 https://doi.org/10.1007/s10529-017-2455-6
  14. Xu L, Xu X, Huang H et al (2018) MiR-1260b promotes the migration and invasion in non-small cell lung cancer via targeting PTPRK. Pathol Res Prac 214, 776-783 https://doi.org/10.1016/j.prp.2018.02.002
  15. Kim J, Wu HH, Lander AD, Lyons KM, Matzuk MM and Calof AL (2005) GDF11 controls the timing of progenitor cell competence in developing retina. Science 308, 1927-1930 https://doi.org/10.1126/science.1110175
  16. Nakashima M, Mizunuma K, Murakami T and Akamine A (2002) Induction of dental pulp stem cell differentiation into odontoblasts by electroporation-mediated gene delivery of growth/differentiation factor 11 (Gdf11). Gene Ther 9, 814-818 https://doi.org/10.1038/sj.gt.3301692
  17. Wu HH, Ivkovic S, Murray RC et al (2003) Autoregulation of neurogenesis by GDF11. Neuron 37, 197-207 https://doi.org/10.1016/S0896-6273(02)01172-8
  18. McPherron AC, Lawler AM and Lee SJ (1999) Regulation of anterior/posterior patterning of the axial skeleton by growth/differentiation factor 11. Nat Genetics 22, 260-264 https://doi.org/10.1038/10320
  19. Andersson O, Reissmann E and Ibanez CF (2006) Growth differentiation factor 11 signals through the transforming growth factor-beta receptor ALK5 to regionalize the anteriorposterior axis. EMBO Rep 7, 831-837 https://doi.org/10.1038/sj.embor.7400752
  20. Oh SP, Yeo CY, Lee Y, Schrewe H, Whitman M and Li E (2002) Activin type IIA and IIB receptors mediate Gdf11 signaling in axial vertebral patterning. Gene Dev 16, 2749-2754 https://doi.org/10.1101/gad.1021802
  21. Gaunt SJ, George M and Paul YL (2013) Direct activation of a mouse Hoxd11 axial expression enhancer by Gdf11/Smad signalling. Devel Biol 383, 52-60 https://doi.org/10.1016/j.ydbio.2013.08.025
  22. Hannan NR, Jamshidi P, Pera MF and Wolvetang EJ (2009) BMP-11 and myostatin support undifferentiated growth of human embryonic stem cells in feeder-free cultures. Clon Stem Cells 11, 427-435 https://doi.org/10.1089/clo.2009.0024
  23. Suragani RN, Cadena SM, Cawley SM et al (2014) Transforming growth factor-beta superfamily ligand trap ACE-536 corrects anemia by promoting late-stage erythropoiesis. Nat Med 20, 408-414 https://doi.org/10.1038/nm.3512
  24. Williams G, Zentar MP, Gajendra S, Sonego M, Doherty P and Lalli G (2013) Transcriptional basis for the inhibition of neural stem cell proliferation and migration by the TGFbeta-family member GDF11. PLoS One 8, e78478 https://doi.org/10.1371/journal.pone.0078478
  25. Tang F, Ling C and Liu J (2018) Reduced expression of growth differentiation factor 11 promoted the progression of chronic obstructive pulmonary disease by activating the AKT signaling pathway. Biomed Pharmacother 103, 691-698 https://doi.org/10.1016/j.biopha.2018.04.091
  26. Fan X, Gaur U, Sun L, Yang D and Yang M (2017) The Growth Differentiation Factor 11 (GDF11) and Myostatin (MSTN) in tissue specific aging. Mech Age Devel 164, 108-112 https://doi.org/10.1016/j.mad.2017.04.009
  27. Poggioli T, Vujic A, Yang P et al (2016) Circulating Growth Differentiation Factor 11/8 Levels Decline With Age. Cir Res 118, 29-37 https://doi.org/10.1161/CIRCRESAHA.115.307521
  28. Davis BN, Hilyard AC, Lagna G and Hata A (2008) SMAD proteins control DROSHA-mediated microRNA maturation. Nature 454, 56-61 https://doi.org/10.1038/nature07086
  29. Kang H, Davis-Dusenbery BN, Nguyen PH et al (2012) Bone morphogenetic protein 4 promotes vascular smooth muscle contractility by activating microRNA-21 (miR-21), which down-regulates expression of family of dedicator of cytokinesis (DOCK) proteins. J Biol Chem 287, 3976-3986 https://doi.org/10.1074/jbc.M111.303156
  30. Kang H, Louie J, Weisman A et al (2012) Inhibition of microRNA-302 (miR-302) by bone morphogenetic protein 4 (BMP4) facilitates the BMP signaling pathway. J Biol Chem 287, 38656-38664 https://doi.org/10.1074/jbc.M112.390898