Liproxstatin-1 is an effective inhibitor of oligodendrocyte ferroptosis induced by inhibition of glutathione peroxidase 4

Bao-You Fan , Yi-Lin Pang , Wen-Xiang Li , Chen-Xi Zhao Yan Zhang Xu Wang Guang-Zhi Ning Xiao-Hong Kong, Chang Liu, Xue Yao , Shi-Qing Feng

Abstract Our previous studies showed that ferroptosis plays an important role in the acute and subacute stages of spinal cord injury. High intracellular iron levels and low glutathione levels make oligodendrocytes vulnerable to cell death after central nervous system trauma. In this study, we established an oligodendrocyte (OLN-93 cell line) model of ferroptosis induced by RSL-3, an inhibitor of glutathione peroxidase 4 (GPX4). RSL-3 significantly increased intracellular concentrations of reactive oxygen species and malondialdehyde. RSL-3 also inhibited the main antiferroptosis pathway, i.e., SLC7A11/glutathione/glutathione peroxidase 4 (xCT/GSH/GPX4), and downregulated acyl-coenzyme A synthetase long chain family member 4. Furthermore, we evaluated the ability of several compounds to rescue oligodendrocytes from ferroptosis. Liproxstatin-1 was more potent than edaravone or deferoxamine. Liproxstatin-1 not only inhibited mitochondrial lipid peroxidation, but also restored the expression of GSH, GPX4 and ferroptosis suppressor protein 1. These findings suggest that GPX4 inhibition induces ferroptosis in oligodendrocytes, and that liproxstatin-1 is a potent inhibitor of ferroptosis. Therefore, liproxstatin-1 may be a promising drug for the treatment of central nervous system diseases.

Key Words: cell death; central nervous system; factor; ferroptosis; oligodendrocyte; oxidation; pathway; repair; spinal cord injury Chinese Library Classification No. R453; R741; Q255 1International Cooperation Base of Spinal Cord Injury, Tianjin Key Laboratory of Spine and Spinal Cord, Department of Orthopedics, Tianjin Medical University General Hospital, Tianjin, China; 2School of Medicine, Nankai University, Tianjin, China

Introduction

After traumatic central nervous system (CNS) injury, significant oligodendrocyte loss occurs as a result of secondary injury (Lytle and Wrathall, 2007; Oyinbo, 2011; Scheller et al., 2017). Death of oligodendrocytes leads to demyelination, which accounts for poor functional recovery. Because of low levels of glutathione (GSH) and high levels of iron, oligodendrocytes are highly susceptible to oxidative damage (Thorburne and Juurlink, 1996; Juurlink et al., 1998). Low glutathione and high iron are also key inducers of ferroptosis, a recently-discovered form of regulated cell death (Dixon et al., 2012). However, ferroptosis in oligodendrocytes has not been well-studied.Glutathione peroxidase 4 (GPX4) is a central regulator of ferroptosis (Yang et al., 2014). In the spinal cord, GPX4 is mainly expressed in neurons and oligodendrocytes, but not in astrocytes (Hu et al., 2019). Numerous studies have investigated the mechanisms of ferroptosis in neurons (Chen et al., 2015; Zhang et al., 2018, 2020; Kenny et al., 2019; Chu et al., 2020). GPX4 plays a pivotal role in neuronal ferroptosis. Knockout of GPX4 in neurons results in ferroptosis (Chen et al., 2015). After spinal cord injury, GPX4 is downregulated, and the ferroptosis inhibitor SRS 16-86 and deferoxamine (DFO) can prevent this reduction in GPX4 and improve the survival of neurons in the injured spinal cord (Yao et al., 2019; Zhang et al., 2019). GPX4 is localized to the nucleus in oligodendrocytesin vivo, in contrast to the neuronal cytoplasmic localization (Hu et al., 2019). However, whether GPX4 also plays a key role in oligodendrocyte survival has not been investigated.

RSL-3 was discovered before ferroptosis, and it increases lethality in the presence of oncogenic Ras. RSL-3 was demonstrated to induce ferroptosis (Yang and Stockwell, 2008). Further research demonstrated that RSL-3 binds to and inhibits GPX4 (Yang et al., 2014). GPX4 is decreased during ferroptosis in intracerebral hemorrhage and spinal cord injury animal models (Zhang et al., 2018, 2019; Yao et al., 2019). Therefore, in this study, we used RSL-3 to investigate ferroptotic cell death induced by GPX4 inhibition in oligodendrocytes.

OLN93 is a permanent oligodendroglial cell line derived from neonatal rat brain. OLN93 cells express typical markers of oligodendrocytes, such as myelin basic protein, myelinassociated glycoprotein and proteolipid protein (Richter-Landsberg and Heinrich, 1996). It is a valid cell model for investigating the proliferation and differentiation of oligodendrocytes (Richter-Landsberg and Heinrich, 1996; Robitzki et al., 2000; Vargas-Medrano et al., 2019). Liproxstatin-1 (Lipro-1) is an inhibitor of ferroptosis, and our previous study demonstrated that DFO can inhibit ferroptosis. Edaravone (EDA) was recently reported to inhibit ferroptosis of hepatoma cellsin vitro(Friedmann Angeli et al., 2014; Homma et al., 2019; Yao et al., 2019). In this study, we further examined the ability of these compounds to inhibit ferroptosis in oligodendrocytes. We established a model of ferroptosis induced by inhibition of GPX4 in OLN93 oligodendrocytic cells, and we compared the effects of different ferroptosis inhibitors, with the aim of helping to advance the development of strategies for inhibiting oligodendrocyte ferroptosis.

Materials and Methods

Cell culture

Immunofluorescence staining

Cells were washed with phosphate-buffered saline (PBS) and fixed with 4% formaldehyde for 10 minutes at room temperature. After washing with PBS, the cells were covered with blocking medium (0.25% Triton X-100 and 5% goat serum in PBS) for 1 hour at room temperature. Then, the cells were incubated with the primary antibodies overnight at 4°C. After washing, the cells were incubated with secondary antibodies for 1 hour at room temperature. 4′,6-diamidino-2-phenylindole (Cat# C0065; Beijing Solarbio Science & Technology, Beijing, China) was used for nuclear staining. Images were captured on a fluorescence microscope (Cat# TH4-200; Olympus, Tokyo, Japan) and analyzed with Image Pro-Plus 6.0 (https://www.mediacy.com/). Primary antibodies included GPX4 (rabbit; 1:100; Cat# ab125006; Abcam, Cambridge, MA, USA), oligodendrocyte transcription factor 2 (Oligo2; goat; 1:200; Cat# F2418; R&D Systems, Minneapolis, MN, USA) and ferroptosis suppressor protein 1 (FSP1, also known as AIFM2; rabbit; 1:200; Cat# BS7655; Bioss, Woburn, MA, USA). Secondary antibodies were Alexa Fluor 488-conjugated goat anti-rabbit IgG (H+L) (1:500; Cat# ab150077; Abcam) and Cy3-labeled goat anti-mouse IgG (H+L) (1:500; Cat# A0521; Beyotime Biotechnology, Shanghai, China).

Cell viability assay

Cells seeded in 96-well plates were used for cell viability assay. To determine the RSL-3 concentration for 50% cytotoxicity, the cells were treated with PBS (0.1%), dimethyl sulfoxide (DMSO; 0.1%; Sigma-Aldrich, St. Louis, MO, USA), or RSL-3 (Cat# S8155; Selleck, Shanghai, China) at 100, 50, 25, 12.5, 6.25, 3.125, 1.5625 or 0.78 μM. Every group had five replicates. After 24 hours of RSL-3 treatment, the medium was replaced with fresh medium (Dulbecco’s modified Eagle medium/nutrient mixture F-12 + 2% fetal bovine serum + 1% penicillin-streptomycin). 3-(4,5-Dimethylthiazolyl-2)-2,5-diphenyltetrazolium bromide (MTT; 10 μL, 5 mg/mL; Cat# M2128; Sigma-Aldrich) was added to each well. After 4 hours, the medium was removed, 150 μL DMSO was added, and the optical density was read at 490 nm with a spectrophotometer (Multiskan; Thermo Fisher Scientific, Waltham, MA, USA). For the determination of mean effective concentration (EC50) of Lipro-1 (Cat# S7699; Selleck), EDA (Cat# IE0020; Beijing Solarbio Science & Technology) and DFO (Cat# D9533; Sigma-Aldrich), the cell viability assay was also used.

Western blot assay

Western blot assay was used to assess the expression of ferroptosis-associated proteins (GPX4, SLC7A11 (xCT) and acylcoenzyme A synthetase long chain family member 4 (ACSL4)) in OLN93 cells treated with RSL-3 to induce ferroptosis. We also examined the effects of Lipro-1. The cells were lysed with radioimmunoprecipitation assay buffer supplemented with phenylmethylsulfonyl fluoride (a protease inhibitor; Cat# ST505; Beyotime Biotechnology) for 30 minutes at 4°C. After centrifugation at 12,000 ×gfor 15 minutes, the supernatant was collected, and a bicinchoninic acid protein assay kit (Cat# P0012S; Beyotime Biotechnology) was used to measure protein concentration. Then, 20 μg of total protein was resolved by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and transferred onto a polyvinylidene difluoride membrane (Cat# BSP0161; Beijing Solarbio Science & Technology). The membrane was blocked with 5% milk in Tris-buffered saline containing 0.1% Tween-20 for 1 hour, and then incubated with primary antibodies at 4°C overnight. After washing with Tris-buffered saline containing 0.1% Tween-20, the membrane was incubated for 1 hour at room temperature with the secondary antibodies. BeyoECL Star (Cat# P0018AM; Beyotime Biotechnology) was used for the detection of the bands. The primary antibodies were GPX4 (1:5000; rabbit; Cat# ab125006; Abcam), xCT (1:5000; rabbit; Cat# ab175186; Abcam), ACSL4 (1:10,000; rabbit; Cat# ab155282; Abcam) and glyceraldehyde 3-phosphate dehydrogenase (1:1000; rabbit; Cat# 2118; Cell Signaling Technology, Danvers, MA, USA). Secondary antibodies were horseradish peroxidase-linked anti-rabbit IgG (1:2000; Cat# 7074; Cell Signaling Technology) and horseradish peroxidase-linked anti-mouse IgG (1:2000; Cat# 7076; Cell Signaling Technology).

Reactive oxygen species detection

A reactive oxygen species (ROS) assay kit (Cat# S0033; Beyotime Biotechnology) was used on cells seeded in 24-well plates. After washing with culture medium (3×), the cells were incubated with 10 mM dichloro-dihydro-fluorescein diacetate and 10 mM Hoechst 33342 (Cat# 14533; Sigma-Aldrich) for 20 minutes at 37°C. The cells were washed three times with warm culture medium. Images were obtained on a fluorescence microscope (Cat# TH4-200; Olympus). ROS levels were calculated based on fluorescence intensity.

GSH detection

For GSH detection, cells were treated with PBS (0.1%), DMSO (0.1%), RSL-3 (7.89 μM) or RSL-3 (7.89 μM) + Lipro-1 (1 μM) for 24 hours. For the RSL-3 + Lipro-1 group, RSL-3 and Lipro-1 were added at the same time. A micro reduced GSH assay kit (Cat# BC1175; Beijing Solarbio Science & Technology) was used to measure the levels of GSH. The cells were collected after digestion and centrifugation, washed with PBS twice, and then lysed with three rounds of freezing and thawing. After centrifugation at 8000 ×gfor 10 minutes, the supernatant was collected. The GSH detection was conducted according to the product manual. The content of GSH in the samples was calculated according to the standard curve.

Malondialdehyde detection

Cells in the PBS (0.1%), dimethyl sulfoxide (DMSO; 0.1%), RSL-3 (7.89 μM) and RSL-3 (7.89 μM) + Lipro-1 (1 μM) groups were used for malondialdehyde (MDA) detection by an MDA assay kit (Cat# BC0025; Beijing Solarbio Science & Technology). Cell pellets were collected by centrifugation, 1 mL extract solution was added, and cells were lysed by ultrasonication. After centrifugation at 8000 ×gat 4°C for 10 minutes, the supernatants were collected and used to detect MDA levels. The optical densities were read at 450, 532 and 600 nm. The amount of MDA was obtained using the formula provided in the product manual.

Propidium iodide staining

Propidium iodide (PI) solution (20 μM in PBS; Cat# P8080; Beijing Solarbio Science & Technology) was used to detect dead cells. Cells in the wells were incubated with 500 μL culture medium supplemented with 50 μL PI solution and 5 μL Hoechst 33342 solution. Then, the cells were incubated at 37°C for 20 minutes. After washing with PBS, the cells were observed with a fluorescence microscope.

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Mitochondrial lipid peroxidation detection

For mitochondrial lipid peroxidation detection, cells were divided into PBS (0.1%), DMSO (0.1%), RSL-3 (7.89 μM) and RSL-3 (7.89 μM) + Lipro-1 (1 μM) groups. 3-[4-(Perylenylphenylphosphino)phenoxy]propyltriphenylphosphonium iodide (MitoPeDPP; Cat# 466; Dojindo Molecular Technologies, Rockville, MD, USA) was used to detect mitochondrial lipid peroxidation. Culture medium was removed, and the cells were washed with PBS. MitoPeDPP working solution (100 μL) was added to each well and incubated at 37°C for 15 minutes in the dark. The supernatant was discarded, and the wells were washed with PBS. PBS with reagent was added, and the cells were observed under a fluorescence microscope.

Statistical analysis

The data are shown as the mean ± standard deviation (SD), and were analyzed using one-way analysis of variance followed by Tukey’spost hoctest. Statistical significance was set atP＜ 0.05. The data were analyzed with GraphPad Prism 7 (GraphPad Software, San Diego, CA, USA).

Results

RSL-3 induces the ferroptosis of OLN93 oligodendrocytes

In the spinal cord, whereas GPX4 localization is mostly cytoplasmic in neurons, it is mainly nuclear in oligodendrocytes (Hu et al., 2019). Ourin vitroexperiment revealed similar nuclear localization of Oligo2 and GPX4 in OLN93 oligodendrocytes by immunostaining (Figure 1A & B), consistent within vivoobservations in the mouse spinal cord (Hu et al., 2019).

After spinal cord injury, GPX4 is downregulated (Yao et al., 2019; Zhang et al., 2019). To examine the effect of GPX4 inhibition on oligodendrocytes, OLN93 oligodendrocytes were incubated with the GPX4 inhibitor RSL-3 at a concentration range of 0-100 μM. The cell viability decreased in a dosedependent manner, and the concentration for 50% cytotoxicity was 7.89 μM for RSL-3 (Figure 1C). PI staining confirmed the RSL-3-induced cell death (Figure 1D). ROS were significantly increased in the RSL-3 group compared with DMSO group (P＜ 0.01; Figure 1E and F).

The ferroptosis pathway is involved in the death of oligodendrocytes

GPX4 is a central regulator of ferroptosis, and its inhibition leads to ferroptosis. After treatment with RSL-3, GPX4 expression was significantly decreased (P＜ 0.01; Figure 2A and B). xCT, another key ferroptosis inhibitor, was also decreased in the RSL-3 group compared with the DMSO group (P＜ 0.05; Figure 2C and D). The ferroptosis marker ACSL4 was reduced in the RSL-3 group compared with the DMSO group (P＜ 0.01; Figure 2E and F). Collectively, these results suggest that key ferroptotic proteins are involved in the cell death of oligodendrocytes.

The EC50 of Lipro-1 is lower than that of EDA or DFO in the ferroptosis model

Figure 1 ｜RSL-3 induces the death of OLN93 oligodendrocytes.

The cytoprotective effects of Lipro-1, EDA and DFO were compared with the MTT cell viability assay. As shown in Figure 3A, Lipro-1 suppressed ferroptosis, with an EC50 of 115.3 nM. EDA also suppressed ferroptosis, with an EC50 of 19.37 μM (Figure 3B). For DFO, the EC50 was 12.04 μM (Figure 3C). These results show that the EC50 of Lipro-1 was the lowest among these compounds (Figure 3D). Furthermore, the percentage of PI-positive cells was lower in the Lipro-1 group than in the RSL-3 group, providing further evidence of an anti-ferroptotic effect of Lipro-1 (P ＜ 0.0001; Figure 3E and F).

Lipro-1 inhibits lipid peroxidation and restores the expression of GSH, GPX4 and FSP1

To further clarify the mechanisms by which Lipro-1 protects against ferroptosis in oligodendrocytes, lipid peroxidation was assessed. Compared with the PBS and DMSO groups, MDA levels were increased in the RSL-3 group (P ＜ 0.0001), but decreased in the RSL-3 + Lipro-1 group (P ＜ 0.001; Figure 4A). Furthermore, Lipro-1 suppressed mitochondrial lipid peroxidation (Figure 4B). We also measured components of the anti-ferroptotic GSH/GPX4 pathway. As shown in Figure 4C, Lipro-1 treatment increased the levels of GSH compared with the RSL-3 group (P ＜ 0.0001). GPX4 was restored to normal levels by Lipro-1 treatment (Figure 4D and E). FSP1, a lipophilic radical-trapping antioxidant (Doll et al., 2019), was decreased by RSL-3. However, in the Lipro-1 group, the expression of FSP1 returned to normal (Figure 4F).

Discussion

We found here that GPX4 inhibition induces ferroptosis in oligodendrocytes, revealing the important role of the protein in oligodendrocyte survival. The key ferroptosis regulators xCT, GSH, GPX4 and ACSL4 were decreased during RSL-3-induced ferroptosis. Lipro-1 was more potent than EDA or DFO in rescuing oligodendrocytes from ferroptosis. Lipro-1 suppressed mitochondrial lipid peroxidation and reduced MDA levels, and it upregulated GSH, GPX4 and FSP1. Lipro-1 may therefore inhibit ferroptosis through these mechanisms.We used OLN93 to investigate ferroptosis in oligodendrocytes. OLN93 is a cell line that expresses oligodendrocyte markers, such as myelin basic protein, myelin-associated glycoprotein, proteolipid protein and Oligo2, but not glial fibrillary acidic protein (Richter-Landsberg and Heinrich, 1996). Numerous studies have used this cell line to investigate various biological processes in oligodendrocytes, such as oxidative stress (Lim et al., 2016; Vargas-Medrano et al., 2019) and the inflammatory response (Askari and Shafiee-Nick, 2019).

Figure 2 ｜The expression of ferroptosis-associated pathway proteins in oligodendrocytes detected by western blot assay.

We successfully induced ferroptosis in OLN93 cells with RSL-3. RSL-3 is a ferroptosis inducer that covalently binds and inhibits GPX4. After treatment with RSL-3, ROS and mitochondrial lipid peroxidation increased, which indicated that the function of GPX4 was suppressed. Our finding is consistent with other studies showing that GPX4 is downregulated by RSL-3 (Shin et al., 2018; Sui et al., 2018). xCT was also downregulated by RSL-3. xCT is a key regulator of ferroptosis (Jiang et al., 2015; Conrad et al., 2016). It is a light-chain subunit of system Xc-, which exchanges cystine in the extracellular space for glutamate. The cystine is then used to synthesis GSH. Thus, a downregulation of xCT would aggravate ferroptosis in oligodendrocytes. Erastin-induced ferroptotic cell death in primary cortical neurons is associated with decreased xCT and GPX4 (Zhang et al., 2020). Thus, the whole ferroptosis system (xCT and GPX4 mainly) is affected during ferroptosis. ACSL4 is a sensitive marker of ferroptosis (Doll et al., 2017). However, ACSL4 was downregulated in the present oligodendrocyte ferroptosis model. Because the dose of RSL-3 used here was based on the half-maximal inhibitory concentration (IC50), the cells were not completely dead. Thus, cells might downregulate ACSL4 to modulate the lipid composition to suppress ferroptosis.

Figure 3 ｜The inhibitory effects of Lipro-1, edaravone and deferoxamine on ferroptosis of OLN93 oligodendrocytes at 24 hours.

Figure 4 ｜Mechanism of Lipro-1-mediated inhibition of ferroptosis in OLN93 oligodendrocytes.

Oligodendrocytes are sensitive to oxidative stress, and are therefore more susceptible to ferroptosis. GSH is consumed by GPX4 to inhibit lipid peroxidation, especially of lipid hydroperoxides within biological membranes (Brigelius-Flohé and Maiorino, 2013). GPX4 protects against lipid peroxidation by converting the reduced GSH into glutathione disulfide and the lipid hydroperoxides or hydrogen peroxide to the corresponding alcohol and/or water (Ursini et al., 1982; Brigelius-Flohé and Maiorino, 2013; Gaschler et al., 2018). However, the levels of GSH in oligodendrocytes are lower than those in astrocytes (Thorburne and Juurlink, 1996), and therefore the GSH/GPX4 system is insufficient to prevent lipid peroxidation. Additionally, the total iron content in oligodendrocyte precursor cells is much higher than that in astrocytes (Thorburne and Juurlink, 1996). Iron is essential for ferroptosis because of its ability to generate ROS via redox reactions (Ray et al., 2012). The increased levels of iron and the inability to inhibit lipid peroxidation are both key factors that render oligodendrocytes sensitive to ferroptosis. Interestingly, the expression of GPX4 is downregulated in spinal cord and brain injuries. Thus, oligodendrocytes are likely to undergo ferroptosis in these diseases, which would in turn aggravate demyelination.

The inhibition of ferroptosis in oligodendrocytes is a promising therapeutic strategy for diseases of the CNS. Several drugs have been used to inhibit ferroptosis in different animal models. Our previous study demonstrated the effectiveness of DFO, an iron chelating agent, in repairing spinal cord injury (Yao et al., 2019). However, that study only examined the protective effect of DFO in neurons. Additionally, anin vitrostudy showed that the free radical scavenger EDA can inhibit ferroptosis (Homma et al., 2019). Lipro-1 was reported to inhibit ferroptosis caused by GPX4 deficiency in the kidney (Friedmann Angeli et al., 2014). Thus, to find the most potent drugs to treat CNS diseases, the effectiveness of Lipro-1, EDA and DFO in suppressing ferroptosis was evaluated. Lipro-1 inhibited ferroptosis at nanomolar concentrations, and was more effective than EDA or DFO. However,in vivoexperiments are needed to rigorously assess the potential of Lipro-1 for the treatment of CNS diseases.

Lipro-1 not only suppressed mitochondrial lipid peroxidation, but also enhanced the anti-ferroptosis pathway. A previous study demonstrated that Lipro-1 could decrease mitochondrial ROS (Feng et al., 2019), consistent with our current results. In particular, Lipro-1 increased GSH to enhance the antiferroptosis system. Furthermore, Lipro-1 restored GPX4 to normal levels in ferroptotic oligodendrocytes. Feng et al. (2019) reported that Lipro-1 could restore the expression of GPX4in vivo. The GPX4 in nuclei can inhibit oxidative damage to the nucleus to rescue cells. Lipro-1 restores GPX4 levels in ONL93 cells to inhibit the ferroptosis signal in the nucleus (Imai et al., 2017). Currently, there is no evidence that GPX4 in the nucleus protects against mitochondrial lipid peroxidation. Recently, Bersuker et al. (2019) and Doll et al. (2019) found that another component of the cellular anti-ferroptosis system, FSP1, can reduce coenzyme Q10 using NAD(P)H, and that the reduced coenzyme Q could trap lipid peroxyl radicals, in turn suppressing lipid peroxidation. RSL-3 downregulated FSP1 in oligodendrocytes here, although the mechanism is still unclear.

There are limitations to this study of oligodendrocyte ferroptosis. First, we used the OLN93 cell line in this preliminary study. Further study may require primary oligodendrocytes or oligodendrocyte progenitor cells. Whether mature oligodendrocytes and oligodendrocyte progenitor cells have different susceptibilities to ferroptosis is an interesting question. The proliferation, differentiation and migration of oligodendrocyte progenitor cells should also be investigated in the pathology of ferroptosis. Moreover, whether ferroptosis occursin vivoin mature oligodendrocytes or oligodendrocyte progenitor cells should be investigated in SCI mouse models. Iron metabolic changes should be also studied in oligodendrocyte ferroptosis because the metal plays a key role in oligodendrocyte maturation and function. After spinal cord injury, oligodendrocytes are severely decreased, and demyelination accounts for poor functional recovery (Grossman et al., 2001). Our previous study showed that the xCT/GSH/GPX4 signaling pathway is significantly impaired (Yao et al., 2019; Zhang et al., 2019). However, whether ourin vitrofindings can be extended toin vivosystems remains an open question. Deferoxamine, an iron chelator, can protect cells from ferroptosis, while liproxstatin-1 maybe works as a ferroptosis saver by inhibiting lipid peroxidation. However, the specific mechanisms behind these two drugs are not still wellknown, so liproxstatin-1 combined with deferoxamine may provide a new insight into mechanism and it may also result in a therapeutically superior effect. And our following research will explore this interesting topic in the near future.

This study is the first investigation on oligodendrocyte ferroptosis induced by the GPX4-specific inhibitor RSL-3. RSL-3 reduced the expression of GPX4, xCT and ACSL4, and lowered GSH levels. We also discovered Lipro-1 was more potent than EDA or DFO in protecting against ferroptosis. Lipro-1 inhibited lipid peroxidation and increased the levels of GSH, GPX4 and FSP1. Our findings offer a novel strategy for treating CNS diseases associated with oligodendrocyte loss.

Author contributions:Study design and manuscript writing: BYF, YLP, WXL, XY, SQF; cells culture, immunostaining, western blot, MDA and GSH detection: BYF, YLP, WXL; MTT, ROS, mitochondrial lipid peroxidation, and PI detection: CXZ, YZ, XW; statistical analysis: GZN, XHK, CL. All the authors approved the final version of the manuscript.

Conflicts of interest:The authors declare no conflicts of interest.

Financial support:This study was supported by the National NaturalScience Foundation of China, Nos. 81672171 (to XY), 81972074 (to XY), 81930070 (to SQF), 81620108018 (to SQF), and 81772342 (to GZN); the National Key R&D Program of China, No. 2019YFA0112100 (to SQF); the Natural Science Foundation of Tianjin of China, No. 19JCZDJC34900 (to XY). The funders had no roles in the study design, conduction of experiment, data collection and analysis, decision to publish, or preparation of the manuscript.

Institutional review board statement:OLN93 cells are a commercial product and are not directly implanted in humans or animals. So this study did not involve ethics issues.

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Peer review:Externally peer reviewed.

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