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MARK/PAR1 kinase is a regulator of microtubule-dependent transport in axons
Correspondence to Eva Marie Mandelkow: mandelkow{at}mpasmb.desy.de
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Abstract |
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Microtubule-dependent transport of vesicles and organelles appears saltatory because particles switch between periods of rest, random Brownian motion, and active transport. The transport can be regulated through motor proteins, cargo adaptors, or microtubule tracks. We report here a mechanism whereby microtubule associated proteins (MAPs) represent obstacles to motors which can be regulated by microtubule affinity regulating kinase (MARK)/Par-1, a family of kinases that is known for its involvement in establishing cell polarity and in phosphorylating tau protein during Alzheimer neurodegeneration. Expression of MARK causes the phosphorylation of MAPs at their KXGS motifs, thereby detaching MAPs from the microtubules and thus facilitating the transport of particles. This occurs without impairing the intrinsic activity of motors because the velocity during active movement remains unchanged. In primary retinal ganglion cells, transfection with tau leads to the inhibition of axonal transport of mitochondria, APP vesicles, and other cell components which leads to starvation of axons and vulnerability against stress. This transport inhibition can be rescued by phosphorylating tau with MARK.
Abbreviations used in this paper: APP, amyloid precursor protein; MAP, microtubule associated protein; MARK, microtubule affinity regulating kinase; RGC, retinal ganglion cell.
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Introduction |
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Microtubule tracks are covered with microtubule associated proteins (MAPs), which contribute to their stabilization that is important for cell shape or neurite outgrowth (Drubin and Kirschner, 1986; Kosik and McConlogue, 1994; Cassimeris and Spittle, 2001; Baas, 2002; Biernat et al., 2002). In addition MAPs can compete with motors for microtubule binding (Lopez and Sheetz, 1993; Hagiwara et al., 1994). Our earlier experiments with CHO cells transfected with tau protein revealed an inhibition of transport, with the consequence that organelles clustered in the cell interior (Ebneth et al., 1998). Analysis of organelle flux showed that both types of microtubule motors (kinesin and dynein) become inhibited by tau, but kinesin is more affected so that dynein dominates. Furthermore, experiments with single molecules showed that elevated concentrations of tau on the microtubule surface leads to a reduced attachment of kinesin (Seitz et al., 2002). Analysis of the transport inhibition by tau in neurons showed that the flux of mitochondria and vesicles containing amyloid precursor protein (APP) down the axon is disturbed, resulting in the degeneration of the axons (Stamer et al., 2002). The results suggested a new relationship between tau and APP, the two proteins which play a key role in Alzheimer's disease.
The kinases and phosphorylation sites of MAPs have been studied extensively in the context of microtubule stabilization and neurodegeneration, especially for the case of tau protein (Garcia and Cleveland, 2001; Lee et al., 2001). Certain kinases are particularly efficient in detaching MAPs from microtubules; the best examples are the microtubule affinity regulating kinase (MARK)/Par1 kinases, which phosphorylate the KXGS motifs in the repeat domains of MAP4, MAP2, or tau (Drewes et al., 1997). Increasing the activation of MARK by expression of MARK or its activating kinase MARKK leads to microtubule breakdown and cell death (Ebneth et al., 1999; Timm et al., 2003). Homologous kinases (PAR-1) play a role in cell polarity development (Kemphues, 2000; Riechmann and Ephrussi, 2001; Cohen et al., 2004) or in neurite outgrowth (Biernat et al., 2002). To study the influence of MAP phosphorylation on vesicle and organelle transport we used different cell models. We generated CHO cells inducibly expressing MARK2, labeled vesicles and organelles with fluorescent markers, and traced them by live cell microscopy. To study the influence of tau phosphorylation on axonal transport in primary retinal ganglion neurons we transfected them with YFP-MARK2 and CFP-tau by adenoviruses. Here, we show that different MAPs have similar inhibitory effects on microtubule-based transport which are relieved by kinases of the MARK family that reduce the level of microtubule-bound MAPs and thus remove obstacles from the microtubule surface. In retinal ganglion cells (RGCs) we demonstrate that the inhibition of axonal transport by tau is rescued by the activity of MARK2, which phosphorylates tau at the KXGS motifs and, thus, detaches it from the microtubule tracks. This has implications for the neurodegeneration in Alzheimer's disease where the phosphorylation of tau by kinases of the MARK family is enhanced.
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50% of the cytoplasm is occupied by mitochondria in control cells, which decreases to 15% after tau transfection. The traffic blockade can be relieved by MARK2, but not by the kinase-dead MARK2 mutant (Fig. 2 e).
MARK facilitates endogenous traffic in cells
Our next aim was to monitor the movement of vesicles or organelles along microtubules and to record the parameters of speed, run length, changes in direction, and how they depend on kinases such as MARK. To test whether the phosphorylation of MAPs and their detachment from microtubules would lead to changes in mobility we expressed MARK2 in a controlled fashion in CHO cells under the inducible tet-on expression protocol (Gossen and Bujard, 2002) and chose early time points of MARK2 expression where the microtubule network was still intact. Fig. 3 a shows the punctate distribution of MARK2. The microtubule network is still intact, and there is no sign of colocalization of MARK2 with microtubules (Fig. 3 b).
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Indeed, when MARK2 is induced by addition of doxycyclin in CHO cells there is a dramatic effect on vesicle behavior (Fig. 4). The predominant MAP in CHO cells is a variant of MAP4, one of the high-molecular weight MAPs that control microtubule dynamics (Bulinski and Borisy, 1980; Olson et al., 1995). If the endogenous MAP4 represents obstacles to vesicles on the microtubule track the detachment of MAP4 should facilitate movement. This is indeed seen in the representative traces of Fig. 4 a. The distances traversed during the observation time are normally small (a few micrometers) because there are many kinks where the vesicles change direction. However, induction of MARK2 leads to much more extended tracks (Fig. 4 b). The instantaneous velocities are not affected by MARK (1 µm/s; Fig. 4 c), but the reversal frequencies decrease by 50% (Fig. 4 d), and the run lengths increase by 50% in both directions (Fig. 4 e). Because MARK2 phosphorylates MAP4 or other MAPs at KXGS motifs in the repeat domain and detaches them from microtubules (Illenberger et al., 1996), these results argue that vesicle movement is facilitated and can indeed be regulated locally on the microtubule surface by MAP phosphorylation. This effect is opposite to the transport inhibition by elevated MAP expression (demonstrated in Fig. 1 by the clustering of mitochondria), so that MAPs and their kinases can be regarded as antagonistic with respect to microtubule-based vesicle trafficking.
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0.8 µm/s), but the run length rises conspicuously (approximately twofold). A similar behavior is found for mitochondria (unpublished data). This means that organelles respond to MARK induction similarly to exocytotic vesicles by increasing the run length but not the local velocity. We further investigated endocytotic vesicles labeled with GFP-ß2-adaptin, one of the cofactors of the AP-2 adaptin complex of clathrin-coated vesicles (Laporte et al., 1999). Because of their high mobility these vesicles generated a strong background throughout the cytoplasm, and they frequently left the plane of focus which made tracking difficult (Fig. 4 h). In the analysis (Fig. 4 i) we, therefore, included only particles moving within the focal plane, with defined start and stop points. Nevertheless, the same picture emerged: MARK induction had almost no effect on the instantaneous velocity (1.1 µm/s) but increased the run length by almost twofold (from 3 to 5 µm).
Effect of MARK on axonal transport
The results described thus far were derived from CHO cells because these cells are readily transfected, the microtubule network can be observed, and the proteins are accessible to biochemical analysis. However, for observing effects of transport inhibition that may matter in neurodegeneration we had to turn to differentiated neurons. After a search for suitable cell types we focused on chicken RGCs. Explants of these cells can be obtained from chicken retinae and develop numerous axons in culture with a well-defined polarity which facilitates the measurement of vesicle and organelle movements. The cells can also be transfected with high efficiency (80%) using adenoviral vectors, enabling one to observe the effects of tau (tagged with CFP), MARK2 (tagged with YFP or CFP), and organelles visualized by live stains. In the following description we focus on two examples, mitochondria (stained with MitoTracker red) and vesicles carrying APP, because APP, like tau, plays a crucial role in AD. They are clearly visualized by confocal microscopy and the influence of tau or MARK2 are easily quantified.
One aim of the experiments is to demonstrate the correlation between MARK activity, tau phosphorylation, and organelle movements in the same cell. In the RGC axons of Fig. 5 mitochondria show a roughly uniform distribution with a density around 0.17 particles/µm (Fig. 5 a). Most of these (55%) move anterogradely while the growth cone is advancing; smaller fractions move retrogradely (26%) or are stationary during the period of observation (24 min; Fig. 5 j). When these cells are transfected with CFP-tau the characteristics of movement change dramatically: over the time of 24 h, most mitochondria leave the axon and accumulate in the cell body because the dynein-mediated retrograde traffic dominates (Fig. 5, d–i). The density of mitochondria in the axons decreases strongly (0.08 particles/µm after 24 h; Fig. 5 c, arrow), the fraction of anterograde movements drops below 10%, and stationary or retrograde particles increase to nearly 50% (Fig. 5 k). This feature corresponds to the clustering of mitochondria in the cell body around the MTOC for CHO or N2a cells (Fig. 1, b, d, and f), and analogous observations apply to other cell organelles (e.g., lysosomes, peroxisomes) or transport vesicles (e.g., APP-containing vesicles; Stamer et al., 2002). Note that in spite of the retrograde flow of mitochondria, the expressed tau can move forward and fills the axon homogeneously, illustrating that the transport of tau (which is part of slow axonal transport; Mercken et al., 1995) differs from the fast axonal transport of vesicles and organelles.
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30%); the fraction of stationary particles decreased (compare Fig. 6 b with Fig. 5 k); and the density of particles increased again. A strong reaction of the 12E8 antibody appeared, revealing that tau was phosphorylated at the KXGS motifs (Fig. 6 c, 2). The phosphorylation of tau was accompanied by its removal from microtubules: if cells transfected with tau and MARK2 (Fig. 6 d, 1) were extracted with Triton X-100 the reaction with antibody 12E8 was lost (Fig. 6 d, 3), indicating that the phosphorylated tau was indeed detached from microtubules, and only traces of unphosphorylated tau remained in the axon (Fig. 6 d, 2). This is in strong contrast to cells not transfected with MARK where extraction by Triton X-100 does not remove tau from microtubules (Fig. 6 e, 1) and tau remains unphosphorylated at KXGS motifs (Fig. 6 e, 2). We conclude that the blockade of traffic was relieved after removing tau from the tracks by phosphorylation at the KXGS motifs. Thus, MARK counteracts the inhibitory effect of tau. This interpretation was checked by several controls. Transfection of RGCs with GFP had only a minor effect, most mitochondria moved anterogradely (50%), only a small fraction were in the pause state (30%), underscoring that GFP is a neutral marker (unpublished data). The same was true for the kinase-dead mutant of MARK2 (Fig. 6 c, 3), indicating that the effect of MARK was due to its kinase activity. Like active MARK2 or GFP, the inactive mutant was also distributed evenly along the axon (Fig. 6 c, 3), and there was no phosphorylation of tau in the repeat domain above background (judging by 12E8 immunofluorescence; Fig. 6 c, 4). Finally, we constructed an adenovirus vector encoding a mutant CFP-tau where all four KXGS motifs were changed into KXGA so that the targets of MARK2 were eliminated. Transfection in RGCs caused a strong inhibition of transport, similar to wild-type tau (compare Fig. 7, a and d with Fig. 5, j and k). However, in this case the cotransfection with MARK2 was not able to induce phosphorylation of tau or to rescue the mobility of mitochondria (compare Fig. 7, b, c, and e with Fig. 6 b), showing that blockage of traffic by tau and rescue by MARK2 requires phosphorylatable KXGS motifs on tau.
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20%) moved retrogradely, and only very few were in a pause state during the period of observation (20 min; Fig. 8). Expression of tau reversed the net flow of APP vesicles so that very few particles remained in the axons after 24 h (only 30% anterograde movements). However, coexpression of tau and MARK2 lead to a partial rescue of the traffic inhibition, the number of vesicles in the axons increased and the net flow became anterograde again (60% of particles). This reversal was not seen with the kinase-dead MARK2 mutant or with the KXGA-tau mutant.
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How can a cell regulate the directional bias? In the first instance this is achieved by the architecture of the polar tracks and the choice of motors and adaptors. Many studies have shown that directed transport can be upset by interfering with microtubule stability or orientation (Morris and Hollenbeck, 1995). Likewise, inactivation or detachment of motors from their tracks or cargoes leads to loss of motion or predominance of other motors (Tanaka et al., 1998; Rahman et al., 1999; Morfini et al., 2002). A further level of traffic control is the quality of the track surface and the MAPs attached to it. Particle motility can be influenced by different types of MAPs (Sato-Harada et al., 1996; Bulinski et al., 1997; Ebneth et al., 1998; Stamer et al., 2002). This effect tends to be inhibitory because the MAPs occlude the binding sites for motors on microtubules, as seen more directly by single-molecule assays (Seitz et al., 2002). The inhibition leads to an overall bias of particle flow toward the cell interior (Fig. 1).
What are the implications of the control chain linking MARK with tau, microtubules, and motors? Because microtubules and tau are present in neuronal cell bodies and axons, the same distribution would be expected for MARK and its activating kinase, which is indeed observed (Timm et al., 2003). After phosphorylation, the detached tau could float in the cytosol (as seen by the diffuse fluorescence of CFP-tau), but in addition the phospho-tau partly attaches to the actin cytoskeleton (Biernat et al., 2002). A similar phenomenon has been reported for phosphorylated MAP2c in dendrites (Ozer and Halpain, 2000). A further point concerns the interference between motors and tau on the microtubule surface. We previously reported that bound tau reduces the average run length of vesicles in cells (Trinczek et al., 1999), and here we show that MARK increases the run length again. This would imply that MARK clears MAPs off the microtubule tracks, either throughout the cell, or at least locally, for example if MARK were bound to the cargo to be transported. In that case the MAPs could mostly remain associated with microtubules, and only a small fraction would need to be lifted locally from the microtubule surface. In addition we know from experiments on single motor molecules that in vitro tau does not decrease the run length of kinesin as such but the attachment frequency (Seitz et al., 2002). This apparent discrepancy with the observations in cells can be explained by assuming that a cargo particle contains several motors which operate additively or even in concert (Vale, 2003). Thus if one motor slips off the track, another could take over; but if the attachment rate is lowered by a MAP the coordination is perturbed, resulting in a shorter run length.
In RGC axons the relationship between MARK, tau, and traffic is more easily observable than in CHO cells because the microtubule polarity is unambiguous, and traffic events can be traced over longer distances and time periods. The main five results for the case of mitochondria are as follows. (1) Normal state: the majority of mitochondria move anterogradely, small fractions move retrogradely or pause, and the density of mitochondria is relatively high (Fig. 5, a and j). (2) After tau transfection the density decreases drastically (because most mitochondria accumulate in the cell body; Fig. 5, a, c, and d–i). The remaining axonal mitochondria are mostly stationary, some move back, and only very few still move anterogradely (Fig. 5 k). The final state is an axon nearly devoid of mitochondria and thus vulnerable to oxidative stress and other insults (Stamer et al., 2002). (3) Additional transfection of the cells with MARK partially relieves the inhibition by tau so that organelles can move more freely again, especially in the forward direction (Fig. 6 b; Fig. 8). (4) The MARK-transfected axons show tau phosphorylated at KXGS sites and extractable by Triton X-100, indicating that tau is detached from microtubules (Biernat et al., 2002; Fig. 6 c, 2 and d, 2 and 3). (5) Mutant tau with unphosphorylatable KXGA motifs induces strong transport inhibition, which cannot be rescued by MARK2 (Fig. 7).
MAPs are often considered as static elements stabilizing microtubules, with additional functions such as cross-linking, spacing, or anchoring of other cell constituents. The dynamic behavior of MAPs is usually considered only within the framework of microtubule growth or shrinkage. In cells, MAPs are predominantly bound to microtubules, supporting the notion of structural elements (Cassimeris and Spittle, 2001). Nevertheless, the redistribution of MAPs among microtubules is remarkably dynamic even when there is no change in overall microtubule polymerization, suggesting that there is a rapid on/off equilibration (Olmsted et al., 1989; Bulinski et al., 2001). The major regulation of MAP-microtubule binding is achieved by phosphorylation. Many protein kinases and phosphorylation sites have been described for MAPs, most of which tend to lower their affinity to microtubules. Phosphorylation of MAPs is enhanced in fetal tissue (when microtubules are more dynamic), in mitosis (when microtubules have to rearrange), during neuronal differentiation, and in pathological conditions such as neurodegeneration in Alzheimer's disease (where tau loses the ability to bind and stabilize microtubules due to hyperphosphorylation; Lee et al., 2001). These observations have focused attention on the role of MAP phosphorylation in modulating microtubule stability. However, because MAPs also occupy space on the tracks of motor proteins it seemed possible that the phosphorylation of MAPs had other functions as well. MAPs, in particular tau, can be phosphorylated by many kinases, and most target sites become highly phosphorylated in Alzheimer's disease and related tauopathies. However, the effects of tau phosphorylation at different sites can be quite variable. The target sites of proline-directed kinases (SP or TP motifs) tend to have weak or moderate effects, whereas the KXGS motifs in the repeat domain have a pronounced ability to detach tau from microtubules. Tau's ability to interfere with transport requires microtubule binding (Seitz et al., 2002). Therefore, it appeared that MARK would be a good candidate for reversing the transport inhibition.
There are four kinases of the MARK family in humans (Manning et al., 2002). They phosphorylate the KXGS motifs in the MAP2/MAP4/tau family in a similar fashion (Drewes et al., 1997). MARK and its homologues (e.g., PAR-1 in C. elegans and Drosophila) are important in establishing asymmetric cell shapes and distributions (Kemphues, 2000; Riechmann and Ephrussi, 2001; Cohen et al., 2004), including NGF-induced neurite outgrowth from neurons (Biernat et al., 2002). The effects of MARK would therefore be visible in various cell types. MARK is itself regulated by phosphorylation of the activation loop by the activating kinase MARKK (Timm et al., 2003). It is thus embedded in a kinase cascade, reminiscent of other cascades that are regulated by intra- or extracellular signals (Cobb and Goldsmith, 2000). Other modes of regulation could be through scaffold proteins such as 14-3-3 (Benton et al., 2002). The triggers of MARK signaling are not well understood, but they appear to include neuronal differentiation signals and oxidative stress (Jenkins and Johnson, 2000; Biernat et al., 2002).
The results summarized in Fig. 9 show that the cell is capable of enhancing the motility of vesicles and organelles by activating the kinase MARK2. This kinase mainly targets the KXGS motifs in MAP4, MAP2, and tau, thereby removing them from the microtubule surface. Conversely, overexpression of MAPs overwhelms the kinase and leads to clogging of tracks and traffic inhibition, independently of the stabilization of microtubules. It is possible that this kinase also explains the phosphorylation-induced enhancement of vesicle motility observed by other authors (Lopez and Sheetz, 1995; Sato-Harada et al., 1996). The mechanism appears to be similar with all cargoes and MAPs studied so far (demonstrated here for the case of VSV-G vesicles, clathrin-coated vesicles, APP-vesicles, lysosomes, and mitochondria; Figs. 4, 6, and 8). It is based on an apparent extension of the run length without change in the instantaneous velocities. This means that the motor activity itself is not affected, but the probability of motor attachment is increased because there are fewer MAPs as obstacles in their way.
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For fluorescent staining of the AP-2/clathrin-coated vesicles, cells were transfected overnight with 1 µg of the EGFP/ß2-adaptin vector (ß2-adaptin gene cloned into the SmaI–BamHI site of pEGFP-C1 (CLONTECH Laboratories, Inc.) using DOTAP (Boehringer). Before data acquisition the chamber was sealed with baysilone (Bayer) to keep the pH of the culture medium constant at pH 7.2–7.4. Temperature was held constant at 35°C by an air stream. Samples were observed with an Axiovert 10 (Carl Zeiss MicroImaging, Inc.) equipped with a 63x/1.4 NA oil-immersion objective and standard fluorescein filters.
Stable transfection of CHO cells
Stably tau transfected CHO cells were generated as described previously (Ebneth et al., 1998). For expressing MAP2c or MAP4-BD in CHO cells, 60% confluent CHO cells were transfected with 2 µg of plasmid DNA pEUHATagMAP4-BD or pEUHAMAP2c encoding MAP4-BD or MAP2c, and Lipofectamine following the manufacturer's protocol (Invitrogen Life Technologies). Stably transfected cells were selected by growing them in 800 µg/ml geneticin (G-418). After incubation for additional 2–3 wk, cells were cloned by limiting dilution and screened for MAP4-BD–or MAP2c-expressing cells by immunofluorescence and PCR.
Adenovirus vectors encoding fluorescent fusion proteins
Recombinant adenoviruses (CFP-htau40, nonphosphorylatable CFP-htau40/KXGA, APP-YFP, APP-mRFP, YFP-MARK2 wild-type, or dominant negative mutant CFP-MARK2/T208A/S212A) were generated following He et al. (1998) (see Online supplemental material).
Live cell light microscopy
RGCs were prepared as described previously (Stamer et al., 2002; see Online supplemental material). For visualizing the transfection of RGCs and the movement of vesicles and organelles the cells were observed on a confocal microscope (model LSM510; Carl Zeiss MicroImaging, Inc.), kept at 37°C by air heating and supplied with 5% CO2. Images were taken every 4 s for tracking of vesicles and every 8 s for mitochondria, using a 63x objective, beam path, and laser settings for YFP, CFP, or rhodamine fluorescence. Error bars in histograms indicate SEM throughout.
Antibodies and dyes
Rat monoclonal anti-tubulin antibody YL1/2 and mouse mAb DM1A were purchased from Serotec and Sigma-Aldrich, and used at 1:2,000. Polyclonal rabbit anti tau-antibody K9JA was purchased from DakoCytomation, mAb 12E8 against tau (phosphorylated KXGS motifs in the repeat domain, Ser 262 and 356) was a gift from P. Seubert (Elan Pharma, South San Francisco, CA), antibodies against peroxisomes were from W. Just (University of Heidelberg, Heidelberg, Germany). The clone of mRFP was provided by R. Tsien (University of California, San Diego, La Jolla, CA). All fluorescent (TRITC, FITC, and AMCA) secondary antibodies were purchased from Dianova.
Immunofluorescence
Cells were fixed in methanol or 4% PFA and incubated with antibodies. Cells were examined with an Axioplan fluorescence microscope (Carl Zeiss MicroImaging, Inc.) equipped with an 100x oil-immersion objective and filters optimized for triple-label experiments (FITC-, TRITC-, and AMCA-fluorescence) or with an LSM510 confocal microscope using a 63x objective. Changes in mitochondrial distribution were quantified by measuring the cell area occupied by mitochondria, compared with the whole cell, after subtracting the area occupied by the nucleus.
Online supplemental material
Online supplemental material describes the generation of adenoviruses and the transfection of retinal ganglion neurons. This is available at http://www.jcb.org/cgi/content/full/jcb.200401085/DC1.
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Acknowledgments |
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The project was supported in part by a grant from the Deutsche Forschungsgemeinschaft.
Submitted: 16 January 2004
Accepted: 30 August 2004
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References |
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0.3 µm and random direction) can also be observed (spots marked by arrowheads). (g) Velocities remain unchanged upon MARK2 induction (
