Glial scar formation resulted from excessive astrogliosis limits axonal regeneration and impairs recovery of function, thus an intervention to ameliorate excessive astrogliosis is crucial for the recovery of neurological function after cerebral ischemia. In this study we investigated the effects of carnosine, an endogenous water-soluble dipeptide (β-alanyl-L-histidine), on astrogliosis of cells exposed to oxygen-glucose deprivation/recovery (OGD/R) in vitro. Primary cultured rat astrocytes exhibited a significant increase in proliferation at 24 h recovery after OGD for 2 h. Pretreatment with carnosine (5 mmol/L) caused G1 arrest of reactive astrocytes, significantly attenuated OGD/R-induced increase in cyclin D1 protein expression and suppressed OGD/R-induced proliferation of reactive astrocytes. Carnosine treatment also reversed glycolysis and ATP production, which was elevated at 24 h recovery after OGD. A marked increase in migration of reactive astrocytes was observed at 24 h after OGD, whereas carnosine treatment reversed the expression levels of MMP-9 and suppressed the migration of astrocytes. Furthermore, carnosine also improved neurite growth of cortical neurons co-cultured with astrocytes under ischemic conditions. These results demonstrate that carnosine may be a promising candidate for inhibiting astrogliosis and promoting neurological function recovery after ischemic stroke.
Cerebral ischemic stroke is a highly disabling and deadly disease worldwide1. Although a portion of patients with stroke can exhibit long-term survival, they will have lifelong disability owing to the low axonal regenerative capacity of the adult central nervous system (CNS)2. The lack of axonal regeneration during the chronic phase following cerebral ischemia is due not to the intrinsic incapacity of the neuron to regenerate but rather to the presence of an adverse environment in the injury3.
Glial scars predominately consist of reactive astrocytes, microglia/macrophages and extracellular matrix molecules that are known to be secreted by reactive astrocytes4,5. Glial scar formation shows polarity towards the injury6 and is beneficial in limiting the expansion of injury. However, it ultimately limits axonal regeneration and impairs recovery of function7,8. In this regard, manipulation of the glial scar may be favorable for neuronal regeneration and functional recovery.
L-Carnosine (β-alanyl-L-histidine) is an endogenous water-soluble dipeptide that can be transported from the plasma to the cerebrospinal fluid through a proton-coupled oligopeptide transporter known as PEPT29,10. In the CNS of vertebrates, carnosine is mainly distributed in glial cells, especially in astrocytes11. Carnosine is a very versatile dipeptide, and it has been postulated to have numerous biological roles such as free radical scavenger, protein glycosylation inhibitor, anti-inflammatory agent and pH buffer12. However, so far, the physiological activity of carnosine in the brain remains to be elucidated. Recently, data obtained in several independent laboratories suggested that carnosine can provide neuroprotection against ischemic injury in the acute phase of stroke13,14,15. However, the role of carnosine in glial scar formation following cerebral ischemia remains unclear. Recent studies from our group and other laboratories have revealed that by inhibiting bioenergy production, carnosine inhibits the proliferation of several cancer cell lines16,17. In addition, we found that carnosine has dual effects on the energy metabolism of cultured astrocytes under physiological and ischemic conditions18,19. Thus, we note that carnosine may have an influence on glial scar formation in response to cerebral ischemia by affecting cell proliferation.
Therefore, the current study was designed to explore whether carnosine could inhibit gliosis and promote neuronal regeneration after ischemia in an in vitro ischemic model and the possible underlying mechanisms.
Materials and methods
Carnosine (β-alanyl-L-histidine), bovine serum albumin, Triton X-100, 5-bromodeoxyuridine, propidium iodide, RNase, sodium pyruvate, rotenone, oligomycin, and carbonyl cyanide p-trifluoromethoxyphenylhydrazone (FCCP) were obtained from Sigma (St Louis, MO, USA). Dulbecco's modified Eagle's medium (DMEM), glucose-free DMEM, fetal bovine serum, horse serum, and B27 were from GIBCO-BRL (Grand Island, NY, USA). Trypsin, poly-D-lysine, penicillin, streptomycin, L-glutamine, lactate dehydrogenase kit, paraformaldehyde, and BCA Protein Assay Kit were purchased from Beyotime Institute of Biotechnology (Nanjing, China). XF assay medium and XF calibrant solution were purchased from Seahorse Bioscience. A rat interleukin 1β (IL-1β) ELISA kit was purchased from Nanjing Jiancheng Bioengineering Institute (China).
Primary cortical astrocyte-enriched culture
All experiments using animals were performed in accordance with the National Institutes of Health Guide for the Care and Use of Laboratory Animals. Primary cultures of cortical astrocytes were prepared from the cortices of neonatal Sprague-Dawley rats as described previously18. In brief, cortices were dissected from the brains under sterile conditions, digested in 0.25% trypsin for 20 min at 37 °C, and then the dissociated cells were seeded in high glucose (4.5 g/L) DMEM supplemented with 10% fetal bovine serum, 2 mmol/L glutamine, 100 U/mL penicillin and 100 μg/mL streptomycin. The cultures were maintained at 37 °C in a humidified atmosphere of 5% CO2/95% air. On d 10–11, the confluent cultures were shaken overnight to minimize microglia contamination. More than 95% of the cultured cells were astrocytes as identified by immunofluorescent staining for GFAP.
Neuron/astrocyte co-cultures were prepared from 1-d-old Sprague-Dawley rat cortices. In brief, the cerebral cortices were digested with 0.125% trypsin for 10 min at 37 °C, and the dissociated cells were seeded at a density of 0.5×105 cells/cm2 in 96-well plates or 25 cm2 flasks previously coated with poly-D-lysine. Cells were cultured in high glucose (4.5 g/L) DMEM supplemented with 7.5% fetal bovine serum, 7.5% horse serum, 2 mmol/L glutamine, 100 units/mL penicillin and 100 μg/mL streptomycin and were maintained in a humidified CO2 incubator (5% CO2, 95% air, 37 °C). After 48 h in vitro, the culture medium was half replaced with special culture medium supplemented with B-27. The medium was changed every 2–3 d. After 10–12 d, the neurons in these cultures sat on the top of a confluent monolayer of astrocytes. The experiments were performed using these cultures.
Oxygen-glucose deprivation and carnosine treatment
The cells were washed twice and incubated in glucose-free DMEM. Then, the cells were transferred into an anaerobic chamber filled with a gas mixture of 95% N2 and 5% CO2 at 37 °C. At the end of OGD, the cells were replaced with normal culture medium and returned to the normal culture condition for an additional 24, 48 or 72 h. In each experiment, cultures exposed to OGD were compared with normoxic controls supplied with DMEM containing glucose and maintained in standard incubation conditions. Carnosine at a concentration of 1 or 5 mmol/L was supplied 30 min before OGD and was present throughout the OGD and recovery process.
Lactate dehydrogenase (LDH) assay protocol
Relative cell proliferation was determined by comparing the total amount of LDH present in cell lysates after 2- or 4-h OGD followed by 24-, 48- or 72-h recovery to LDH present in cell lysates of controls as described previously20. Total LDH present in cell lysates was measured with an LDH kit according to the manufacturer's instructions. LDH metabolism was quantified by measuring absorbance at 490 nm and 600 nm in a Thermo Scientific Varioskan Flash.
BrdU immunofluorescent staining
To further assess proliferation of glial cells in culture, cells were incubated with 30 μmol/L 5-bromodeoxyuridine (BrdU) after OGD. After the experiments, the cells were fixed with 4% paraformaldehyde for 10 min and then were washed in PBS for 3 min, and the DNA was denatured by incubating in 2 mol/L HCl for 0.5 h. After being washed twice in 0.1 mol/L borate buffer (pH 8.5) and three times in PBS, cells were blocked with 3% BSA for 1 h. Then, cells were incubated in mouse monoclonal antibody against BrdU (1:600, CST, USA) overnight. After being washed twice with PBS, cells were then incubated with goat anti-mouse IgG (1:300, Invitrogen, USA) for 0.5 h. After further washing in PBS, cells were mounted and observed under fluorescence microscopy (Nikon Eclipse TI, Japan). Cell number was counted by NIH ImageJ software.
Immunostaining was also performed in cultured astrocytes and neurons. Cells seeded on coverslips were fixed with 4% paraformaldehyde for 10 min and incubated in 3% bovine serum albumin containing 0.1% Triton X-100 for 1 h. Then, primary antibodies in 3% BSA were applied for 1 h or overnight. For astrocytes and neurons, mouse anti-GFAP (1:300, CST, USA), rabbit anti-Neu (1:200, Abcam, USA), and rabbit anti-beta III Tubulin (1:200, Abcam, USA) were used. After repeated washes in PBS, cells were incubated with Cy3-labeled goat anti-mouse IgG (1:300, Invitrogen, USA) or Alexa Fluor 488-labeled goat anti-rabbit IgG (1:300, Invitrogen, USA) for 0.5 h at 37 °C. After further washing in PBS, cultures were dried, coverslipped, and mounted on glass slides. Finally, the stained cells were observed under fluorescence microscopy (Nikon Eclipse TI, Japan).
Enzyme-linked immunosorbent assay (ELISA) for IL-1β
After OGD/R and carnosine treatment, the supernatants of the cultures were collected and stored at -80 °C until the measurement of IL-1β concentrations. This was done according to the manufacturer's protocol using commercial rat ELISA kits for IL-1β. Absorbance was measured on a microplate reader (Thermo Scientific Varioskan Flash). IL-1β level was determined using standard curves method.
Determination of ATP production
The ATP assay was performed as described previously13. Briefly, the cells were lysed with a lysis buffer followed by centrifugation at 10 000×g for 2 min at 4 °C. Finally, in 6-well plates, the level of ATP was determined by mixing 20 μL of the supernatant with 100 μL of luciferase reagent, which catalyzed the light production from ATP and luciferin. Luminance was measured by a monochromator microplate reader. Standard curves were also generated and the protein concentration of each group was determined using the BCA protein assay kit. Total ATP levels were expressed as nmol/mg protein.
Cell migration assay
Cell migration was assayed using fibronectin-coated polycarbonate filters (8-μm pore size, Transwell; Becton Dickinson, USA). In brief, 1×105 cells/wells containing 1% FBS medium were added to the top compartment. The lower chambers were filled with 600 μL of DMEM supplemented with 10% FBS. The astrocytes were allowed to migrate for 48 h; then, the filters were washed with PBS, fixed with ice-cold 4% paraformaldehyde and stained with DAPI, and observed under fluorescence microscopy (Nikon Eclipse TI, Japan).
Western blot analysis
Western blot analysis was carried out by standard protocol. The following antibodies were used: mouse anti-GAPDH (Abcam, 1:1000), mouse anti-tublin (Abcam, 1:1000), mouse anti-GFAP (CST, 1:1000), rabbit anti-cyclin D1 (Abcam, 1:1000), rabbit anti-MMP 9 (Abcam, 1:1000), and horseradish-conjugated goat anti-mouse antibody or horseradish-conjugated goat anti-rabbit antibody.
Cell cycle analysis
Cell cycle analysis was performed by propidium iodide (PI) staining. Astrocytes were trypsinized and washed with ice-cold PBS (pH 7.4) and fixed in ice-cold 70% ethanol. The cells were then washed with PBS, treated with 500 U/mL RNase at 37 °C for 30 min, and finally stained with PI in PBS. Ten thousand cells were counted for each data point. Cell cycle analysis was performed using a flow cytometer.
Extracellular flux technology
The oxygen consumption rates (OCRs) of astrocytes in different conditions were measured using a Seahorse XF96 Extracellular Flux Analyzer. This instrument allows for the sensitive measurement of glycolysis and multiple parameters of mitochondrial function, including basal OCR, spare respiratory capacity, maximal OCR, ATP-linked respiration and proton leak from adherent intact cultured cells. After baseline measurements, OCRs were measured after sequentially adding to each well oligomycin (1 μg/mL), FCCP (1 μmol/L) and rotenone (1 μmol/L). All assays were conducted using a seeding density of 1×104 cells/well in 200 L of DMEM in a poly-D-lysine-coated XF 96-cell culture microplate. The cells were switched to unbuffered DMEM (carnosine was absent) supplemented with 2 mmol/L sodium pyruvate 1 h prior to the beginning of the assay and maintained at 37 °C.
Neurite growth quantification
The lengths of neurites in each neuron were traced manually and quantified using NIH ImageJ software. Mean neurite length for each neuron was determined for 50–100 neurons per condition from three separate experiments.
Statistical analyses were performed using SPSS 11.5 for Windows. All data were presented as the mean±SD. One-way ANOVA (analysis of variance) followed by LSD (least significant difference) or Dunnett's T3 post hoc test (where equal variances were not assumed) was applied for multiple comparisons, whereas Student's t-test was used for comparisons between two groups. P<0.05 was taken to indicate statistically significant effects.
Effect of OGD/R times on the proliferation of cultured astrocytes
Total LDH content assay and BrdU labeling were used to explore appropriate OGD/R time points that can induce astrocytes to present glial scar characteristics. Combined with the previous experiments by our group18,21, two intermediate durations of OGD and three recovery time points were tested. We found that the total LDH content of astrocytes returned to the control level when exposed to 4-h OGD followed by 24-h recovery, while 2-h OGD and 24-h recovery induced a significant increase in total LDH content (Figure 1A). Next, we tested three recovery time points with 2-h OGD treatment. The total amount of LDH present in cell lysates was 139% of controls after 24-h recovery, but with recovery for 48 h and 72 h, the total amounts of LDH were not significantly different from the controls (Figure 1B). Simultaneously, for further verification, BrdU immunostaining was also carried out. The results showed that OGD for 2 h and recovery for 24 h could induce the most obvious astrogliosis (Figure 1C, 1D), which was consistent with the LDH content detection results. To further ensure that OGD/R caused reactive astrocytes, immunohistochemistry and Western blot analysis were also performed to confirm the high expression of GFAP, which has been recognized as a characteristic of reactive astrocytes. We found that the expression of GFAP was increased remarkably after 2-h OGD and 24-h recovery (Figure 1E and 2D, 2E). In addition, we found that the released IL-1β, one of the most extensively studied proinflammatory cytokines that has been suggested to play an important role in astrogliosis22, was markedly increased (169% of control, Figure 2F) after OGD/R treatment. Thus, the duration of 2 h for OGD and 24 h for recovery was used in the following experiments.
Carnosine suppressed reactive gliosis of astrocytes induced by OGD/R in vitro
The effect of carnosine on the reactive gliosis of cultured astrocytes was determined via total LDH content detection and BrdU staining. Compared with the OGD/R group, treatment with 1 and 5 mmol/L carnosine significantly decreased the total amount of LDH present in cell lysates (Figure 2A). In the BrdU staining assay, we found that the percentage of BrdU-positive astrocytes was significantly decreased in the carnosine-treated group (OGD/R group: 133%±14.9%; Carnosine+OGD/R group: 110%±15.7%, P<0.01; Figure 2B, 2C). The change of the expression level of GFAP protein in the astrocytes under the influence of 5 mmol/L carnosine was also determined by Western blotting, and the results showed that carnosine treatment partly reversed the increase in GFAP expression induced by OGD/R (Figure 2D, 2E). In addition, the OGD/R-induced increase in IL-1β release by astrocytes was reversed by carnosine treatment (OGD/R group: 1.77±0.25; Carnosine+OGD/R group: 1.23±0.21, P<0.05; Figure 2F), indicating that the functional properties of reactive astrocytes were altered by carnosine. Thus, all the data suggested that carnosine may suppress the reactive gliosis of astrocytes induced by OGD/R.
Carnosine inhibited cell cycle progression and regulated the expression of cyclin D1 proteins in astrocytes exposed to OGD/R
To explore whether the inhibitory effect of carnosine on the proliferation of astrocytes is related to its action on the cell cycle, we performed a flow cytometry assay (FACS). As shown in Figure 3A and 3B, OGD/R significantly decreased the number of cells in G1 phase and increased the number of cells in S phase. Carnosine treatment almost completely reversed the decrease in the number of cells in G1 phase (OGD/R group: 74.1%±1.82%, Carnosine+OGD/R group: 81.2%±2.07%, P<0.05) and the increase in the number of cells in S phase (OGD/R group: 16.8%±1.98%, Carnosine+OGD/R group: 9.6%±3.24%, P<0.05), indicating that carnosine induces G1 arrest in reactive astrocytes induced by OGD/R by inhibiting the G1-to-S phase transition. Next, we measured the protein expression levels of cyclin D1, the critical transition protein that is required for progression from G1 into S phase23. The results showed that carnosine treatment reversed the increase in cyclin D1 protein expression induced by OGD/R (Figure 3C, 3D). Thus, these results suggest that carnosine inhibited reactive gliosis of astrocytes may be due at least in part to its ability to suppress the G1-to-S phase transition.
Effect of carnosine on mitochondrial bioenergetics and glycolysis of cultured astrocytes exposed to OGD/R
Energy metabolism is also closely related to cell proliferation. Therefore, in this study, we also investigated the effects of carnosine on the oxygen consumption rate and extracellular acidification rate in cultured astrocytes exposed to OGD/R. The results showed that OGD for 2 h and recovery for 24 h increased the basal cellular oxygen consumption rates (OCRs) and extracellular acidification rates (ECARs) to 341.4±56.3 pmol·min·−1μg−1 protein (∼138% of control, Figure 4A, 4C), and 91.58±18.21 mpH·min·−1μg−1 protein (∼217% of control, Figure 4B, 4D), respectively. The mitochondrial respiration and non-mitochondrial respiration of cultured astrocytes exposed to OGD/R were both increased significantly. In addition, OGD/R treatment caused a marked increase both in ATP-linked respiration and proton leak of cultured astrocytes (Figure 4C). Carnosine treatment did not affect the multiple parameters of mitochondrial respiration (Figure 4C), whereas it markedly reversed the increase in ECARs induced by OGD/R in cultured astrocytes (Figure 4D). In addition, we found that carnosine treatment significantly reversed the increase in ATP production induced by OGD/R in cultured astrocytes (Figure 4E).
Carnosine suppressed migration of astrocytes exposed OGD/R in vitro
A cell migration assay was used to ascertain the effect of carnosine on the migration of cultured astrocytes. Compared with the control group, the number of astrocytes migrating through the film increased significantly (274% of control) after OGD/R. However, when 5 mmol/L carnosine was added to the culture medium, the increased migration could partly be inhibited (53% of OGD/R group, Figure 5A, 5B). These results suggested that carnosine is probably involved in regulating migration of astrocytes exposed to OGD/R. Then, we used Western blotting technology to test the expression level of matrix metalloproteinases-9 (MMP-9), which is closely related to cell migration24. The results showed that the expression level of MMP-9 in astrocytes after OGD/R increased significantly when compared with control group, while carnosine treatment could cut high levels of MMP-9 in cells after OGD/R (Figure 5C, 5D). Thus, the effect of carnosine on migration levels of reactive astrocytes may be related to its modulation effect on MMP-9.
Carnosine improved neurite growth in neuron-astrocyte co-cultures
To study the effect of carnosine on neurite growth, we also detected the neurite length by immunofluorescence staining of class III β-tubulin in control, OGD/R and carnosine-treated cells. We found that the mean length of neurites was prominently shorter than the controls following 2-h OGD and 24-h recovery, whereas carnosine treatment significantly improved the inhibited growth of neurites (Control group: 223.87±59.06, OGD/R group: 78.92±43.41, OGD/R+Carnosine group: 163.75±59.47, P<0.01, Figure 6).
Glial scar formation in the later stage of cerebral ischemia is an important factor affecting the nervous function recovery of patients. In the current study, we demonstrated for the first time that carnosine can inhibit the proliferation and migration of reactive astrocytes induced by OGD/R in vitro. Moreover, we also found a direct effect of carnosine on axonal regeneration in neuron/astrocyte co-cultures exposed to OGD/R.
Cerebral ischemia-induced widespread progressive alterations of astrocytes, which include cell hypertrophy, up-regulation of GFAP expression, and increased proliferation capability, are commonly known as reactive astrogliosis25. Here, we found that after 2 h OGD and 24 h reperfusion, the percentage of BrdU+ astrocytes significantly increased, and the expression of GFAP and the release of IL-1β were also markedly up-regulated, indicating that OGD/R can induce astrocytes to present glial scar characteristics. Therefore, an OGD/R-induced in vitro model of glial scar that can be controlled easily and conveniently can be used to explore the mechanisms underlying glial scar formation and to find new ways to improve brain repair and functional recovery after stroke.
Recently, an inhibitory effect of carnosine on the proliferation of several transformed and neoplastic cells has been reported by our group and others13,26,27,28. In the present study, we found that carnosine treatment significantly reduced the number of BrdU+ astrocytes 24 h after OGD. Simultaneously, the enhanced expression of GFAP protein induced by OGD/R was also partly reversed by carnosine, indicating that carnosine treatment also inhibited the proliferation of reactive astrocytes induced by OGD/R. It has been reported that carnosine acts as a regulator of cell cycle in cancer cells. Iovine et al showed that carnosine induces G1 arrest in human HCT116 colon cancer cells by inhibiting the G1/S phase transition28. Interestingly, we also found that carnosine was capable of suppressing the transformation of reactive astrocytes from G1 phase to S phase and decreasing the cyclin D1 protein level. Thus, besides cancer cells, carnosine may also inhibit the proliferation of normal cells with increased proliferative capacity, and the underlying mechanism may be at least partly due to its action on the cell cycle and cyclin-dependent kinases.
It was also reported that the anti-proliferation effect of carnosine on tumor and cancer cells is related to its ability to suppress glycolytic activity and/or mitochondrial energy of the cells13,26. Our recent study also revealed that carnosine exerts biphasic modulation on energy metabolism of cultured cortical astrocytes under normal and ischemic conditions18. Thus, it seems that cellular energy metabolism is considered a target of carnosine. Data from the Seahorse XF96 Extracellular Flux Analyzer demonstrated that OGD/R-induced reactive astrocytes had higher ATP-linked oxygen consumption rates and basal ECARs, indicating that both mitochondrial bioenergetics and glycolysis pathways are activated in reactive astrocytes for the increased energy demand to facilitate cell proliferation. Carnosine could not reverse the increase in mitochondrial respiration, but it significantly reversed the increase in ECARs in reactive astrocytes. Carnosine has been recognized as a pH buffer, and carnosine in the culture medium can affect monitoring for ECARs. Therefore, in this study, we washed the cells carefully to avoid residual carnosine before the cells were switched to unbuffered DMEM. In the current study, the data also showed that carnosine can partly reverse the increase in ATP production induced by OGD/R in reactive astrocytes. Thus, the data indicate that it is the glycolysis, but not the mitochondrial bioenergetics pathway, involved in the carnosine action on the proliferation of reactive astrocytes. Stephanie et al have reported that carnosine adversely affects fermentative growth of Saccharomyces cerevisiae in glucose, while aerobic growth on glycerol is not inhibited, suggesting that the metabolism-dependent effects of carnosine are mediated by different mechanisms29. In addition, it has been reported that during mid-to-late G1, a nutrient-sensitive cell growth checkpoint controls progression to S phase. The cell must prepare for division in G1 by synthesizing macromolecules needed for biomass duplication. Mitotically committed cells thus up-regulate the glycolytic activator fructose-2,6-bisphosphatase 3 (PFKFB3) at the nutrient-sensitive checkpoint and block glycolysis to impair the passage through this restriction point. Thus, the glycolysis pathway may be involved in carnosine's action on G1 arrest/decreased expression of cyclin D1 in reactive astrocytes.
Astrocyte migration is a key step in glial scar formation after cerebral ischemia30, and weaker astrocyte migratory activity contributes to neuroprotection31. In the current study, we found that the migratory activity of reactive astrocytes could be suppressed by carnosine. It has been reported that astrocyte migration is regulated by multiple factors, such as MMP-9, which degrades extracellular matrix components and plays important roles in a variety of biological and pathological processes32. Here, we found that OGD/R markedly up-regulated MMP-9 expression in astrocytes, whereas expression of MMP-9 was significantly suppressed by carnosine treatment. Our results are consistent with previous findings that carnosine inhibits metastasis of SK-Hep-1 cells via inhibition of MMP-9 expression33. Thus, our data suggest that in addition to cancer cells, carnosine may also inhibit the migration of normal cells by reducing MMP-9 expression in these cells.
Previously, it was demonstrated that the growth of neuronal axons is often arrested after stroke34,35. In the current study, following 24-h recovery after OGD, the neurons exposed to OGD with astrocytes showed abortive regeneration, as they attained much shorter mean neurite lengths, and their morphologies were also consistent with neurons responding to an inhibitory environment induced by other injuries6,34. Thus, these data suggest that astrocytes at 24-h recovery after 2-h OGD exhibit a glial scar-like action to inhibit neuron growth. However, Wang et al reported that astrocytes at 48-h recovery after OGD present a glial scar-like action36. The discrepant results from these two different experiments are probably due to the use of distinctly different neuron/astrocyte co-culture models. In the current study, we also found that the neurite growth inhibition was markedly reversed by carnosine. Boato et al reported that increased local levels of IL-1β exerted detrimental effects on lesion size and glial activation as well as on the plasticity of CNS axons in vivo after injury22. Thus, the positive action of carnosine on neurite growth was probably partly due to the inhibitory effect of carnosine on the release of IL-1β from the activated astrocytes, or other direct or indirect actions of carnosine on the proliferation and migration of the reactive astrocytes.
In conclusion, our results showed that carnosine reduced proliferation and migration of reactive astrocytes induced by OGD/R by arresting the cell cycle at the G1/S phase, suppressing glycolysis and ATP production and regulating MMP-9 expression. Also, carnosine treatment led to better axonal regrowth in neuron/astrocyte co-cultures under ischemic conditions. Taken together, these results suggest that carnosine may be a good candidate as a therapeutic agent for brain functional recovery following cerebral ischemia.
Yao SHEN and Jian-xin LYU conceived and designed the experiments; Li OU-YANG and Yao SHEN wrote the manuscript; Li OU-YANG, Yuan LIU and Bing-yu WANG performed experiments and analyzed the data; Pei CAO, Jing-jing ZHANG and Yu-yan HUANG performed the experiments.
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This work was supported by the National Natural Science Foundation of China (81571289).
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Ou-yang, L., Liu, Y., Wang, By. et al. Carnosine suppresses oxygen-glucose deprivation/recovery-induced proliferation and migration of reactive astrocytes of rats in vitro. Acta Pharmacol Sin 39, 24–34 (2018). https://doi.org/10.1038/aps.2017.126
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