Importin alpha-importin beta complex mediated nuclear translocation of insulin-like growth factor binding protein-5

  • Sun Min
    Department of Dermatology, Xiangya Hospital, Central South University, Changsha, China
  • Long Juan
    Department of Dermatology, Xiangya Hospital, Central South University, Changsha, China
  • Yi Yuxin
    Department of Dermatology, Xiangya Hospital, Central South University, Changsha, China
  • Xia Wei
    Department of Dermatology, University of Michigan, Ann Arbor, MI, USA

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タイトル別名
  • Importin α-importin β complex mediated nuclear translocation of insulin-like growth factor binding protein-5

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説明

Insulin-like growth factor-binding protein (IGFBP)-5 is a secreted protein that binds to IGFs and modulates IGF actions, as well as regulates cell proliferation, migration, and apoptosis independent of IGF. Proper cellular localization is critical for the effective function of most signaling molecules. In previous studies, we have shown that the nuclear IGFBP-5 comes from ER-cytosol retro-translocation. In this study, we further investigated the pathway mediating IGFBP-5 nuclear import after it retro-translocation. Importin-α5 was identified as an IGFBP-5-interacting protein with a yeast two-hybrid system, and its interaction with IGFBP-5 was further confirmed by GST pull down and co-immunoprecipitation. Binding affinity of IGFBP-5 and importins were determined by surface plasmon resonance (IGFBP-5/importin-β: KD=2.44e-7, IGFBP-5/importin-α5: KD=3.4e-7). Blocking the importin-α5/importin-β nuclear import pathway using SiRNA or dominant negative impotin-β dramatically inhibited IGFBP-5-EGFP nuclear import, though importin-α5 overexpress does not affect IGFBP-5 nuclear import. Furthermore, nuclear IGFBP-5 was quantified using luciferase report assay. When deleted the IGFBP-5 nuclear localization sequence (NLS), IGFBP-5ΔNLS loss the ability to translocate into the nucleus and accumulation of IGFBP-5ΔNLS was visualized in the cytosol. Altogether, our findings provide a substantially evidence showed that the IGFBP-5 nuclear import is mediated by importin-α/importin-β complex, and NLS is critical domain in IGFBP-5 nuclear translocation.

収録刊行物

  • Endocrine Journal

    Endocrine Journal 64 (10), 963-975, 2017

    一般社団法人 日本内分泌学会

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