Page:Human wild-type full-length tau accumulation disrupts mitochondrial dynamics and the functions via increasing mitofusins.pdf/2

https://www.nature.com/srep/ of fusion proteins attenuates apoptosis. These observations suggest that intracellular accumulation of tau may cause neurodegeneration through disrupting mitochondrial functions, but the direct evidence for the role of wild-type full-length human tau in mitochondrial dynamic is still lacking.

Mitochondria, as dynamic organelles, regulate cell viability and morphology of the synapses,. The mitochondrial dynamics is regulated by continuous fusion and fission,. The fusion is regulated by mitofusins namely Mfn1 and Mfn2, the integral membrane proteins of the mitochondrial outer membrane, and optic atrophy type 1 (OPA1), an inner mitochondrial membrane associated protein,. In yeast, exogenous expression of the mammalian homologues of Fis1 (hFis1 for human homologues) induces mitochondrial fragmentation, whereas in mammalian cells, dynamin like protein 1 (DLP1) plays a key role in mitochondrial fission and mitochondrial fission factor (Mff) functions as an essential factor for mitochondrial recruitment of DLP1 during fission. The mitochondrial dynamics determines mitochondrial morphology, size, distribution and functions. These observations suggest that intracellular accumulation of tau may antagonize acute apoptosis via modulating mitochondria fission/fusion and cause neurodegeneration through disrupting mitochondrial functions.

In the present study, we investigated whether and how htau is involved in mitochondria dysfunction and neurodegeneration. We show that overexpression of htau protein disrupts mitochondrial dynamics and the functions with a correlated reduction of cell viability and neurodegeneration, the mechanisms involve an enhanced fusion by an increased mitofusin accumulation.

Intracellular tau accumulation enhances mitochondrial fusion without affecting their fission We have previously reported that intracellular accumulation of tau affects cell viability. To explore the molecular mechanisms, we further investigated here the influence of tau on mitochondria, the vital organelle known for the essential role in energy metabolism and cell viability. We first measured mitochondrial dynamics in cells with stable expression of human tau or the vector (termed as S293tau and S293vec). A photo-convertible fluorescence protein, mito-Dendra2, was co-expressed to track mitochondrial dynamic in living cells. The cells show green signal under a low laser power (5%) at 24 h after expression of mito-Dendra2 (Fig. 1a). Then we selected several transfected cells with the similar morphology and applied higher laser power (50%) to a defined region of interest (ROI) in transfected cells to allow full photo-conversion of the mitochondria (from green to red). The fusion of a red mitochondrion with a green one generated a yellow mitochondrion. By measuring the percentage of red mitochondria that became yellow over time as an overall index for fusion events, we found that the average time for all red mitochondria in ROI to turn yellow is 27.6 ± 5.2 min in S293vec cells, whereas the average time was less than 16 ± 3.0 min in S293tau cells (Fig. 1a,b). The accelerated time for all red mitochondria in ROI to turn yellow was also observed in the cells with transient expression of htau (Fig. 1c). Since mitochondria fusion was affected by mitochondria mobility and velocity, we also assayed the mitochondria mobility and velocity in S293vec and S293tau cells. We found that the percent of moving mitochondria increased in S293tau cells and the retrograde movement of mitochondria in S293tau cells was higher than that of S293vec (Fig. S1). These data indicate that htau enhanced retrograde mitochondrial transport rate and fusion, which may explain the perinuclear mitochondrial accumulation.

Overexpression of htau induces perinuclear accumulation of mitochondria Then, we measured the cellular distribution and the morphologies of mitochondria (Fig. S2). In majority of S293vec cells (86.0 ± 8.0%), the mitochondria were uniformly distributed throughout the cytoplasm and only 12.5 ± 6.9% the cellular area was devoid of mitochondria. In contrast, in the majority of S293tau cells (79.8 ± 5.5%), the mitochondria were accumulated in the perinuclear area and the area devoid of mitochondria was increased to 39.9 ± 3.8% (Fig. 2a–c). As to the morphology, 73.9 ± 5.9% S293tau cells showed elongated mitochondria with an average length of 8.5 ± 5.0 μm, whereas 79.8 ± 4.1% S293vec cells exhibited short tubular structure with an average length of 3.6 ± 1.5 μm and only 4.0 ± 1.6% cells showed elongated mitochondria (Fig. 2d,e).

Apparent perinuclear accumulation of mitochondria with an increased length was also shown at 24 h after transient expression of htau (Fig. 2f–j). Microtubule stability was detected with no significant change of the acetylated α-tubulin level at 24 h after overexpression of htau, although an increased level of the acetylated α-tubulin was seen at 12 h (Fig. S3b), and no significant microtubule disruption was detected at 24 h (Fig. S3a), suggesting that the mitochondria impairment was independent of the microtubule disruption. Furthermore, the accumulation of mitochondria was also detected in rat primary hippocampal neurons cultured for 7 days in vitro (div) by co-expressing mito-DsRed2 and eGFP-tagged htau for 24 h (Fig. 2k–m). These data together strongly suggest that expression of htau enhances mitochondrial fusion and promotes their accumulation.

Overexpression of htau impairs mitochondrial functions and causes neurodegeneration We also observed that transient expression of htau decreased ATP level and the ratio of ATP/ADP, and as well as inhibited the complex I activity at 72 h (Fig. 3a–c), consequently, a remarkable reduction of cell viability was shown at 72 h (Fig. 3d). In the cells with stable expression of htau (S293tau) or the vector (S293vec), the ATP level, the ratio of ATP/ADP, the complex I activity, and the cell viability were all decreased at 72 h (Fig. S4a–d). These data confirm that overexpression of htau disrupts mitochondrial functions and reduces cell viability. Interestingly, an increased cell viability was detected at 48 h (Fig. S5), which supports our previous finding that overexpression of tau rendered the cells anti-apoptosis at early stage. In rat primary hippocampal neurons cultured for 7 div, overexpression of htau for 48 h induced severe retraction or loss of neuronal processes (Fig. 3e,g). By time-lapse recording, retraction of the cell processes was shown after stable (Fig. 3f,h, and Supplementary video 1 and 2) or transient expression of htau for 48 h (Fig. S6). These data indicate that overexpression of htau causes neurodegeneration. SCIENTIFIC REPORTS