NFAT/Fas signaling mediates the neuronal apoptosis and motor side effects of GSK-3 inhibition in a mouse model of lithium therapy (original) (raw)
Chronic lithium administration to mice results in decreased brain GSK-3 activity and impaired motor coordination. In order to explore the potential deleterious consequences of chronic lithium administration to mice, we first established a protocol of LiCl administration in food pellets resulting in serum lithium concentrations within the upper range of the therapeutic window for treatment and prophylaxis of BD. To achieve this, we gradually increased the dose of lithium over an 8-week period (Figure 1A). In good agreement with our previous observations (20), feeding mice with a food pellet preparation containing 1.7 g LiCl/Kg for 2 weeks resulted in 0.64 ± 0.04 mM plasma concentration of lithium (Figure 1B). Subsequently, mice were shifted to a food pellet preparation containing 2.5 g LiCl/kg for 6 more weeks, during which serum lithium concentrations were monitored every week. As shown in Figure 1B, plasma levels were above 1.0 mM by week 3 and progressively increased over the following 3 weeks, when they reached a plateau at 1.2 mM.
Reduced brain GSK-3 activity and impaired motor coordination induced by chronic lithium administration at therapeutic doses. (A) Diagram showing lithium administration protocol. (B) Lithium plasma levels across the 8 weeks of feeding with lithium-containing chow (n = 38). conc, concentration. (C) Upper panels: Western blot detection and quantification of inactive GSK-3 (pSer21/9-GSK-3) in homogenates from striatum of control and lithium-treated mice (control [C], n = 8; lithium, n = 8). Lower panels: Western blot detection of phosphorylated tau (PHF-1) in homogenates from striatum (St) and cortex (Cx) of control and lithium-treated mice. (D) Body weight over the course of treatment in control (n = 16), lithium-treated (n = 24), and calorie-restricted (diet, n = 8) mice. (E) Descent time in vertical pole test (control, n = 28; lithium, n = 25; diet, n = 8). (F–H) Analysis of gait parameters in footprint test as measured by DigiGait system (control, n = 23; lithium, n = 17; diet, n = 8): stride length variability (F), step angle variability (G), and stance asymmetry (H). *P < 0.05, **P < 0.01, ***P < 0.001 versus control; #P < 0.05, ##P < 0.01 versus diet.
We then verified that this lithium administration paradigm resulted in decreased GSK-3 activity in brain (Figure 1C). Western blot analysis of brain homogenates from control and lithium-treated mice was performed using antibodies that recognize inactive GSK-3 (phosphorylated at serines 21 and 9 of GSK-3α and β, respectively) and with antibodies that recognize GSK-3 (α or β isoforms) regardless of phosphorylation state. In good agreement with previous reports of lithium administration in vivo (30), an increase in phospho–GSK-3 was observed in brain homogenates of the lithium-treated mice (Figure 1C). Western blot analysis of tau phosphorylation at the GSK-3–dependent epitope PHF-1 (11) further confirmed decreased brain GSK-3 activity as a consequence of lithium administration (Figure 1C).
Upon completion of this 8-week lithium administration paradigm that results in decreased brain GSK-3 activity, mice were subjected to motor behavior testing. Since chronic lithium administration in mice is known to decrease body weight (35), and body weight can affect performance in many behavioral tests (36), we also analyzed in parallel a group of mice subjected to caloric restriction to match the 10%–15% body weight loss observed in the lithium-treated mice (Figure 1D).
We have previously reported that transgenic mice with decreased GSK-3 activity (Tet/DN-GSK-3 mice) perform poorly in striatum-dependent motor tasks, such as the vertical pole test and the footprint test (34), while showing normal global motor activity in the open field test (34). Accordingly, we analyzed the lithium-treated mice in the vertical pole test and in the DigiGait apparatus, which measures footprint pattern and other parameters of walking regularity (Figure 1, E–H). In good agreement with the data from Tet/DN-GSK-3 mice, the vertical pole test revealed that lithium-treated mice spent twice the amount of time descending the pole compared with control mice (9.75 ± 0.78 seconds versus 18.8 ± 1.77 seconds; P < 0.001), while the diet-subjected mice were indistinguishable from the control mice (Figure 1E). Lithium-treated mice also showed multiple gait abnormalities as measured with the DigiGait apparatus, such as increased variability in stride length (Figure 1F), increased variability in step angle (Figure 1G), and stance asymmetry (Figure 1H). These gait abnormalities are commonly found in patients and in mouse models of motor disorders such as Parkinson disease, Huntington disease, and amyotrophic lateral sclerosis (ALS) (37–39). Importantly, no gait abnormalities were observed in mice subjected to caloric restriction. Finally, in good agreement with the data from Tet/DN-GSK-3 mice, lithium-treated mice showed normal levels of global locomotion in the open field (data not shown). We can thus conclude that mice with serum lithium concentrations within the high therapeutic range for BD treatment show decreased brain GSK-3 activity accompanied by subtle motor side effects.
Neuronal apoptosis induced by chronic lithium administration. We then tested whether, as found in transgenic mice with decreased GSK-3 activity (34), the lithium administration paradigm that decreases GSK-3 activity and causes motor coordination deficits in wild-type mice also induces apoptosis in brain regions involved in motor control. To this end, we performed immunohistochemistry using an antibody that recognizes the active (cleaved) form of caspase-3 on brain sections of mice that had been subjected to the 8-week administration paradigm and behavioral testing described above. As shown in Figure 2, A–G, most of the analyzed brain regions from lithium-treated mice showed increased numbers of cleaved caspase-3–positive cells compared with controls. These include cortex, striatum, globus pallidus, hippocampus, and cerebellum (Figure 2, A–G). In contrast, amygdala, thalamus, and superior colliculus showed no significant difference (Figure 2G and data not shown). The most significant increases were observed in cortex and striatum, with 1.8- and 1.92-fold increases in the number of apoptotic neurons as compared with controls, respectively (Figure 2G). A similar pattern of lithium-induced apoptosis across brain regions was found when the incidence of apoptosis was analyzed by TUNEL staining (Figure 2, H–L). It is worth noting that levels of lithium-induced apoptosis detected using this technique were much higher in the cerebellum and slightly higher in the cortex, striatum, globus pallidus, and hippocampus than those obtained with cleaved caspase-3 staining.
Neuronal apoptosis induced by chronic lithium administration. (A–F) Immunohistochemical detection of cleaved caspase-3–positive cells in cortex (A, E, and F) and striatum (B, C, and D) of control (A and B) and lithium-treated (C–F) mice. Insets show higher magnifications of the boxed areas. I–VI, layers of the cortex; cc, corpus callosum; CPu, caudate putamen; NAc, nucleus accumbens; ac, anterior commissure. Scale bar in A: 200 μm (A–F). (G) Immunohistochemical quantification of the number of cleaved caspase-3–positive cells per 30-μm sagittal section in regions analyzed (n = 22 per group, 4 sections per animal). GP, globus pallidus; Hipp, hippocampus; Thal, thalamus; Cb, cerebellum. (H–K) Representative images of TUNEL staining in cortex (H–I) and striatum (J and K) of control (H and J) and lithium-treated (I and K) mice. Scale bar in H: 200 μm (H–K). (L) Quantification of the number of TUNEL-positive cells per 30-μm sagittal section in the different regions analyzed (control, n = 12; lithium, n = 10). (M–R) Representative images of double-labeling immunofluorescence with anti–cleaved caspase-3 and anti-NeuN (M and N), GFAP (O and P), or Iba-1 (Q and R) antibodies in striatal sections of lithium-treated mice. Scale bar in M: 10 μm (M–R). White arrows indicate double-labeled cells; open arrows, caspase-3–positive/GFAP-negative cells. (S) Histogram showing quantification of double staining with caspase-3 antibody (Casp-3) and markers of different cellular types (n = 8 per group). *P < 0.05, **P < 0.01, ***P < 0.001.
Finally, to investigate which cell types exhibit lithium-induced apoptosis, we performed double immunofluorescence with the cleaved caspase-3 antibody and with markers of specific subpopulations. More precisely, we used antibodies directed at neuronal (NeuN), astrocytic (glial fibrillary acidic protein [GFAP]), and microglial (Iba1) markers (Figure 2, M–S). Across the entire brain, the NeuN-positive subpopulation of caspase-3–positive cells was the only one that increased in lithium-treated mice. In fact, of the total cleaved caspase-3–positive cells in lithium-treated mice, 94% were positive for NeuN (Figure 2S). Therefore, we can conclude that lithium-induced apoptosis essentially occurs in neurons.
Neuronal translocation of NFAT transcription factors by lithium. We next addressed the potential mechanisms by which chronic lithium and concomitant GSK-3 inhibition results in neuronal apoptosis. There is extensive literature indicating the dual role of GSK-3 inhibition in modulating apoptosis (see ref. 40 for a recent review). Briefly, it has been shown that GSK-3 inhibition prevents cell death induced by multiple apoptotic stimuli including growth factor withdrawal, DNA damage, glutamate toxicity, and many others (40). However, when apoptosis is triggered by activation of death domain–containing receptors such as Fas or the TNF receptor (i.e., when this is executed through the extrinsic pathway of apoptosis) (41), GSK-3 inhibition potentiates the apoptotic effect (40). This was first evidenced by the lithium-induced increase in TNF-mediated toxicity to mouse tumor cells (42). Subsequently, GSK-3β–knockout mice were found to die embryonically due to hypersensitivity to TNF-induced apoptosis in the liver (43). This proapoptotic effect of GSK-3 inhibition was later extended to the other ligands of death domain–containing receptors such as TRAIL (44, 45). Finally, and with regard to neurons, apoptosis induced by activation of the Fas receptor was also found to be potentiated by several GSK-3 inhibitors including lithium (46).
We sought a possible link between GSK-3 inhibition and stimulation of the extrinsic pathway. Interestingly, it has been reported that GSK-3 inhibition promotes nuclear translocation of the nuclear factor of activated T cells c (NFATc) family of transcription factors in various cell types (47, 48), including primary cultured neurons (49). On the other hand, NFAT-mediated transcription is known to control expression of Fas ligand (FasL), the apoptosis initiator that activates Fas receptor (50). This led us to hypothesize the following mechanism by which chronic lithium administration may lead to neuronal apoptosis (Supplemental Figure 1; supplemental material available online with this article; doi:10.1172/JCI37873DS1). First, chronic lithium administration induces sustained GSK-3 inhibition, which, in turn, results in nuclear translocation of NFAT transcription factors and a subsequent increase in FasL production. Finally, the subsequent activation of the cognate receptor Fas initiates apoptosis via the extrinsic pathway. Accordingly, we designed a series of experiments to explore this hypothesis.
Since expression of NFATc-1, -2, -3, and -4 has been reported in brain based on in situ hybridization (51), we performed immunohistochemistry with antibodies against each of them in brain sections from control and lithium-treated mice. None of the tested NFATc2 antibodies yielded specific staining (data not shown). NFTAc1 antibodies recognized only a small subset of astrocytes in a small number of regions such as the globus pallidus and the hippocampus, with no obvious effect of lithium regarding nuclear translocation or total number of NFATc1-positive cells (data not shown). In good agreement with previous reports showing NFATc3 and NFATc4 expression in neurons (49, 52, 53), both NFATc3 and NFATc4 antibodies yielded a neuronal pattern in all brain regions analyzed (Figure 3, A and B).
Increased nuclear localization of NFAT transcription factors in lithium-treated mice. (A) Representative images of NFATc4 immunohistochemistry in cortex and striatum of control and lithium-treated mice. Arrows indicate neurons with NFATc4 staining in the nucleus. (B) Representative images of NFATc3 immunohistochemistry in cortex and striatum of control and lithium-treated mice. Arrows indicate neurons with NFATc3 staining in the nucleus. Insets show higher magnifications of the cells marked with bold arrows. Scale bars in A and B: 100 μm. (C and D) Representative confocal microscope images showing a 1-μm-deep cortical area subjected to double immunofluorescence with NFATc4 antibody and NeuN antibody (to confirm neuronal identity) and DAPI counterstaining (to verify the nuclear localization) in control (C) and lithium-treated (D) mice. (E) Number of neurons exhibiting NFATc4 staining in the nucleus per section in regions analyzed (n = 8 per group). (F and G) Representative images of double immunofluorescence with NFATc3 and NeuN antibodies combined with DAPI nuclear counterstaining in cortex of control (F) and lithium-treated (G) mice. Scale bar: 15 μm (C–G). (H) Number of neurons exhibiting NFATc3 staining in the nucleus per section in regions analyzed (n = 8 per group). (I and K) Western blot detection of NFATc3 (I) and NAFTc4 (K) in total, cytoplasmic, and nuclear homogenates from cortex of control and lithium-treated mice (n = 12 per group). Hsp90 (total and cytoplasmic) and lamin B1 (nuclear) antibodies were assayed as loading control. Histograms represent quantification of total, cytoplasmic, and nuclear NFATc3 and NFATc4 corrected by the loading control. (J and L) Nuclear/cytoplasmic (nuc/cyt) ratio of NFATc3 (J) and NFATc4 (L). All histograms in I–L represent lithium values as a percentage compared with the control group. *P < 0.05, **P < 0.01, ***P < 0.001.
The specificity of the employed NFATc3 and NFATc4 antibodies was confirmed by staining brain sections from NFATc3- and NFATc4-knockout mice (Supplemental Figure 2), and the neuronal identity of NFATc3- and NFATc4-positive cells was confirmed by double immunofluorescence with the neuronal marker NeuN (Figure 3, C–G). In untreated mice, both NFATc3 and NFATc4 antibodies yielded only cytoplasmic staining in the vast majority of neurons (control panels in Figure 3, A and B, and Figure 3, C and F), with the number of NFATc4-positive neurons being higher than that of NFATc3-positive neurons (compare control panels in Figure 3A with control panels in Figure 3B). Interestingly, as anticipated in our working hypothesis, lithium treatment resulted in a significant increase in the number of neurons in which NFATc4 and NFATc3 staining was also present in the nucleus (see lithium panels in Figure 3, A, B, D, E, G, and H). Nuclear localization was verified by confocal microscope analysis of brain sections subjected to NFAT/NeuN double immunofluorescence and DAPI-nuclear counterstaining (Figure 3, D and G). These data are in good agreement with a previous report of increased nuclear levels of NFATc4 as a consequence of decreased GSK-3 activity in cultured neurons (49). Importantly, except for the hippocampus, there is a good correlation between the brain regions that show increased neuronal apoptosis and those showing increased nuclear staining of the NFAT transcription factors. Such is the case for cortex, striatum, globus pallidus, and cerebellum. Accordingly, the amygdala, thalamus, and superior colliculus showed neither increases in apoptosis nor nuclear translocation of NFAT transcription factors (Figure 3, E and H, and data not shown).
Apart from an increase in the number of neurons with nuclear NFATc3 and NFATc4, the above-described immunostainings (Figure 3, A–G) may also show an increase in the overall levels of both transcription factors as a result of chronic lithium treatment. To further confirm the increased nuclear translocation of NFATc3 and NFATc4 in response to lithium and to properly address the possible overall increase, we performed Western blot analysis with nuclear and cytoplasmic fractions as well as with total homogenates from control and lithium-treated mice. As shown in Figure 3I, total NFATc3 levels were not increased in brain of lithium -treated mice. Interestingly, NFATc3 levels were significantly decreased in the cytoplasmic fraction of lithium-treated mice. This, together with a trend toward increased NFATc3 levels in the nuclear fraction, resulted in a significant increase in NFATc3 nuclear/cytoplasmic ratio as a consequence of lithium administration (Figure 3J). In the case of NFATc4 and in good agreement with the above-mentioned observation in immunohistochemistry and immunofluorescence experiments, Western blot analysis of total homogenates showed a trend toward increased overall levels in lithium-treated mice (Figure 3K). Interestingly, this effect of lithium fits well with the reported role of GSK-3 in decreasing NFATc4 stability by promoting its ubiquitination (54). Despite the apparent increase in NFATc4 in total homogenates, we still observed slightly lower levels of NFATc4 in the cytosolic fraction of lithium-treated mice. This, together with the increased levels observed in the nuclear fraction of lithium-treated mice, led to a significant increase in NFATc4 nuclear/cytoplasmic ratio as a consequence of lithium administration (Figure 3L). In summary, the Western blot analysis of NFATc3 and NFATc4 in total homogenates showed no change in the overall NFATc3 level and a tendency toward increased NFATc4 levels in response to chronic lithium. More importantly, the analysis of nuclear and cytoplasmic fractions confirmed the lithium-induced increase in NFATc3 and NFATc4 nuclear translocation observed by immunohistological methods, with the increased difference between control and lithium-treated mice likely due to enrichment of the sample following nuclear isolation.
Increased FasL after chronic lithium correlates with GSK-3 inhibition and nuclear NFAT translocation. To explore whether the increased nuclear translocation of NFAT transcription factors resulted in increased FasL in brain of lithium-treated mice, we performed Western blot and immunohistochemical studies. Western blot revealed an increase in levels of both full-length FasL and the soluble shed form (sFasL) in the striatum of lithium-treated mice (Figure 4, A and B). In the cortex, the full-length form was also increased, by 42%, in lithium-treated mice (n = 5, P < 0.05), while no significant changes were detected in the shed form (data not shown). In good agreement with these findings, FasL immunohistochemistry revealed a significant increase in the number of FasL-positive cells in the striatum and globus pallidus of lithium-treated mice (Figure 4, C–F). A tendency toward increased numbers of FasL-positive cells was also observed in the cerebellum of treated mice, though this effect did not reach statistical significance (Figure 4F). The cortex, despite showing increased FasL levels by Western blot, showed no difference in the number of FasL-positive cells. This may be due to the fact that this brain structure, apart from showing the highest number of positive cells (Figure 4F), also contained the cells with the strongest labeling compared with any other brain region (Figure 4C). It therefore seems that the cortical cells susceptible to an increase in FasL levels upon lithium-induced NFAT translocation are already above the threshold for detection by immunohistochemistry in untreated mice.
Level of FasL and number of FasL-positive neurons are increased in chronic lithium-treated mice. (A and B) Western blot detection (A) and quantification (B) of the full-length and shed soluble form of FasL (FasL and sFasL, respectively) in striatal cytoplasmic fraction of control and lithium-treated mice (n = 5 per group). (C–E) FasL immunohistochemistry in brain sections from lithium-treated mice. Micrographs show positive cells in cortex (C), striatum (D), and globus pallidus (E). Scale bars: 40 μm (C) and 30 μm (D and E). (F) Histogram showing quantification of FasL-immunoreactive cells in control and lithium-treated mice in regions analyzed (n = 16 per group). (G) Histogram showing quantification of double staining with FasL antibody and markers of specific cell types (n = 8 per group). (H–N) Representative images of double-labeling immunofluorescence in striatum of lithium-treated mice: with anti-FasL (H) and anti-NeuN (I) antibodies; with anti-FasL (J) and anti-NFATc4 (K) antibodies; and with anti-FasL (L) and anti–pSer21/9-GSK-3a/β antibodies (M). N is a merge of the images in L and M. Scale bars: 20 μm (H and I); 20 μm (J and K); 10 μm (L–N). *P < 0.05, **P < 0.005, ***P < 0.002.
In good agreement with previous reports (52, 55), the vast majority of brain FasL-immunoreactive cells appeared to be neurons based on their morphology (Figure 4, C–E). To confirm this observation and further explore the role of GSK-3 inhibition and subsequent NFAT nuclear translocation in the lithium-induced increase in FasL-positive cells, we performed double labeling immunofluorescence studies on striatal sections of lithium-treated mice. As shown in Figure 4, G–I, 95% of the FasL-positive cells were confirmed to be neurons by double labeling with the neuronal marker NeuN. Furthermore, striatal FasL-positive neurons coincide with those showing nuclear staining of NFAT (Figure 4, J and K) and were also detected with an antibody that recognizes phospho–GSK-3 (pSer21/9-GSK-3, Figure 4, L–N). The fact that GSK-3 inactivation, NFAT nuclear translocation, and FasL immunostaining all coincide in the same subset of neurons strongly suggests that these events are functionally related and support our mechanistic hypothesis.
Blockade of NFAT nuclear translocation by cyclosporin A prevents lithium-induced motor deficits and -apoptosis. To explore whether the above-described NFAT/FasL changes in lithium-treated mice are in fact responsible for the lithium-induced neuronal apoptosis and maybe also for the motor deficits, we decided to perform similar experiments with lithium-treated mice in which we interfered with NFAT and/or FasL signaling (see Supplemental Figure 1C). Regarding NFAT, the effect of GSK-3 on cytoplasmic/nuclear shuttling of NFAT transcription factors is balanced by calcineurin activity. Briefly, GSK-3 phosphorylates conserved NFAT serine residues necessary for NFAT nuclear export and therefore promotes NFAT nuclear exit (47). On the contrary, calcineurin dephosphorylates those conserved serine residues, thus favoring NFAT nuclear translocation, which can be prevented with the calcineurin inhibitor cyclosporin A (CsA) (48, 56). We thus reasoned that CsA administration during the last days of the lithium treatment paradigm could be used to prevent the lithium-induced nuclear translocation of NFAT transcription factors. If this nuclear NFAT translocation is indeed required for the neurotoxicity and motor behavioral consequences of lithium, these should be diminished by CsA administration. Accordingly, we established a protocol of CsA administration in drinking water during the last 1.5 weeks of lithium treatment (Figure 5A) that fully prevented the above-described lithium-induced nuclear translocation of NFAT transcription factors, as evidenced by immunohistochemistry and confocal analysis of immunofluorescence with DAPI nuclear counterstaining (Figure 5, B and C).
CsA administration impedes NFAT nuclear translocation and prevents chronic lithium-induced apoptosis and motor deficits. (A) Diagram showing lithium and CsA administration protocol in mice. (B) Immunohistological detection of NFATc4. Upper panels show representative immunohistochemistry images in cortex and striatum. Lower panels show confocal microscope images (1 μm) of double immunofluorescence with NeuN together with DAPI nuclear counterstaining in cortex. Left and right panels correspond to lithium- and lithium plus CsA–treated mice, respectively. Arrows indicate neurons with NFATc4 staining in the nucleus, and insets in the upper panels show higher magnifications of the cells marked by bold arrows. Scale bars: 100 μm (upper panels) and 15 μm (lower panels). (C) Number of neurons exhibiting NFATc4 staining in the nucleus per section in regions analyzed (n = 4 per group). (D) Number of cleaved caspase-3–positive cells per 30-μm sagittal section in regions analyzed (control, n = 19; lithium, n = 19; control + CsA, n = 12; lithium + CsA, n = 12). (E) Descent time in vertical pole test (control, n = 20; lithium, n = 17; control + CsA, n = 19; lithium + CsA, n = 20). (F–H) Gait analysis. Stride length variability (F), step angle variability (G), and stance asymmetry (H) in footprint test as measured by DigiGait system (control, n = 15; lithium, n = 12; control + CsA, n = 16; lithium + CsA, n = 16). *P < 0.05, **P < 0.01, ***P < 0.001 versus control; #P < 0.05 versus lithium + CsA.
We then analyzed the effect of CsA administration on apoptosis by immunohistochemical detection of cleaved caspase-3. As shown in Figure 5D, CsA administration did not affect the incidence of apoptosis in control mice. More importantly, the lithium-induced increase in apoptosis described previously was no longer detected in any brain region of CsA-treated mice.
Finally, we also analyzed the effect of CsA administration on the previously described lithium-induced motor deficits. As shown in Figure 5E, CsA administration significantly improved the performance of lithium-treated mice in the vertical pole test, whereas no effect was observed on the performance of control mice. Similarly, while deficits in walking pattern observed with the DigiGait apparatus in lithium-treated mice (increased stride length variability, increased step angle variability, and stance asymmetry) were corrected by CsA treatment, no effect was observed in control mice (Figure 5, F–H). These results, together with the data indicating apoptosis prevention by CsA treatment, strongly suggest that NFAT nuclear translocation contributes to lithium-induced neuronal apoptosis and motor deficits.
Fas-deficient mice are resistant to the neuronal apoptosis and motor side effects of chronic lithium administration. If our working hypothesis is true, the increased incidence of apoptosis in lithium-treated mice should eventually be due to the activation of the death receptor Fas. To investigate whether FasL signaling is also relevant to the observed neurotoxic effects of lithium, we analyzed apoptosis and motor behavior after chronic lithium administration in Fas receptor–deficient mice (lpr mice; ref. 57). In these mice, the lithium dosing paradigm described for wild-type mice (Figure 1A) resulted in serum lithium concentrations slightly greater than 1.5 mM by week 4 (data not shown), thus exceeding the therapeutic window in humans. This is attributable to the compromised renal function of lpr mice (58). For this reason, we slightly modified the dosing paradigm to achieve lithium plasma levels equivalent to those obtained in wild-type mice (Figure 6, A and B).
Fas-deficient (lpr) mice are resistant to chronic lithium-induced neuronal apoptosis and do not show the motor coordination deficits observed in wild-type mice. (A) Diagram showing lithium administration protocol to wild-type and lpr mice. (B) Lithium plasma levels over the 8-week treatment in wild-type and lpr mice (WT, n = 22; lpr, n = 13). (C) Number of cleaved caspase-3–positive cells per 30-μm sagittal section in regions analyzed in wild-type and lpr mice (WT control, n = 10; WT lithium, n = 9; lpr control, n = 7; lpr lithium, n = 7). (D) Descent time in vertical pole test (WT control, n = 20; WT lithium, n = 17; lpr control, n = 19; lpr lithium, n = 20). (E–G) Stride length variability, step angle variability, and stance asymmetry in footprint test measured by DigiGait system in control or lithium-treated WT and lpr mice (WT control, n = 27; WT lithium, n = 21; lpr control, n = 16; lpr lithium, n = 11). *P < 0.05, **P < 0.01, ***P < 0.001, versus WT control; #P < 0.05, ##P < 0.01, ###P < 0.001 versus lpr lithium.
Using cleaved caspase-3 immunostaining, we analyzed the incidence of apoptosis in wild-type and lpr mice following the 8-week dosing paradigm. Interestingly, the increases in apoptosis observed in the cortex, striatum, globus pallidus, hippocampus, and cerebellum of lithium-treated wild-type mice were absent in lithium-treated lpr mice (Figure 6C). These findings thus demonstrate that neuronal apoptosis induced by chronic lithium is mediated by the Fas receptor.
We then decided to compare the motor effects of lithium in lpr and wild-type mice. We first verified that untreated lpr mice did not show any confounding signs of altered global activity or anxiety. For this, we performed the open field test and found that global locomotor activity and the time in center versus periphery shown by lpr mice were indistinguishable from those observed in wild-type mice (data not shown). Interestingly, the lithium-induced motor coordination deficit (detected in the vertical pole test; Figure 6D) and the gait abnormalities (detected with the DigiGait apparatus; Figure 6, E–G) observed in wild-type mice were absent in lithium-treated lpr mice. These results, apart from demonstrating a role of Fas signaling in lithium-induced neurotoxicity, strongly suggest that neuronal loss contributes to the motor side effects of chronic lithium administration.