Bimolecular fluorescence complementation; Lighting-up tau-tau interaction in living cells

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Abstract

Abnormal tau aggregation is a pathological hallmark of many neurodegenerative disorders and it is becoming apparent that soluble tau aggregates play a key role in neurodegeneration and memory impairment. Despite this pathological importance, there is currently no single method that allows monitoring soluble tau species in living cells. In this regard, we developed a cell-based sensor that visualizes tau self-assembly. By introducing bimolecular fluorescence complementation (BiFC) technique to tau, we were able to achieve spatial and temporal resolution of tau-tau interactions in a range of states, from soluble dimers to large aggregates. Under basal conditions, tau-BiFC cells exhibited little fluorescence intensity, implying that the majority of tau molecules exist as monomers. Upon chemically induced tau hyperphosphorylation, BiFC fluorescence greatly increased, indicating an increased level of tau-tau interactions. As an indicator of tau assembly, our BiFC sensor would be a useful tool for investigating tau pathology. © 2013 Tak et al.

Figures

  • Figure 1. Establishment of HEK293-tau-BiFC cell line. (a) N- and C-terminal constituents of Venus protein was fused to fulllength tau (441 a.a.). (b) Basal fluorescence intensity of tau-GFP and tau-BiFC cell line. Scale bar = 200 μm. (c) Expression and basal phosphorylation levels of tau-GFP and tau-BiFC cell line. Immunoblot with anti-tau (ser 262) antibody indicates the expression levels of total tau and immunoblot with anti-tau phospho (ser 396) antibody indicates the basal level of phosphorylated tau. Antiactin indicates loading controls.
  • Figure 2. Cellular distributions of HEK293-tau-GFP (a) and HEK293-tau-BiFC (b). Cells were incubated with nocodazole or vinblastine (3 μM) for 30 min and fluorescence images were taken. Scale bar = 10 μm.
  • Figure 3. Maturation of tau-BiFC upon tau phosphorylation. (a) Diagram of BiFC maturation upon tau phosphorylation. (b) Tau-BiFC cells were incubated with okadaic acid (30 nM) and forskolin (20 μM) for 24 hrs. Scale bar = 200 μm. (c) Quantification of BiFC-fluorescence increase at various time points. (d-f) For the immunoblot assay, tau-BiFC cells were incubated with compounds for 24 hrs and cell lysates were prepared. Black arrows indicate full-lenth tau, red arrows indicate tau dimers, and blue arrows indicate tau fragments. (g-h) The relative amount of phosphorylated tau including its cleaved forms was normalized with that of nonphosphorylated tau (TauSer262). Error bars indicate s.d. from two independent experiments.
  • Figure 4. Cellular distribution of tau-BiFC fluorescence. (a) HEK293-tau-GFP control (b) HEK293-tau-BiFC cells were incubated with each compound for 24 hrs.

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Tak, H. J., Haque, M. M., Kim, M. J., Lee, J. H., Baik, J. H., Kim, Y. S., … Kim, Y. K. (2013). Bimolecular fluorescence complementation; Lighting-up tau-tau interaction in living cells. PLoS ONE, 8(12). https://doi.org/10.1371/journal.pone.0081682

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