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Retroviral expression of human arginine decarboxylase reduces oxidative stress injury in mouse cortical astrocytes.

Hong S, Son MR, Yun K, Lee WT, Park KA, Lee JE - BMC Neurosci (2014)

Bottom Line: The neuroprotective effects of ADC seemed to be related to its ability to attenuate expression of iNOS and MMPs.Our findings imply that astrocytes can be reinforced against oxidative stress by endogenous agmatine production through ADC gene transduction.The results of this study provide new insights that may lead to novel therapeutic approaches to reduce cerebral ischemic injuries.

View Article: PubMed Central - PubMed

Affiliation: Brain Korea 21 Project for Medical Science, and Brain Research Institute, Department of Anatomy, Yonsei University College of Medicine, 50 Yonsei-ro, Seodaemun-gu, Seoul 120-752, Republic of Korea. jelee@yuhs.ac.

ABSTRACT

Background: In physiologic and pathologic conditions of the central nervous system (CNS), astrocytes are a double-edged sword. They not only support neuronal homeostasis but also contribute to increases in neuronal demise. A large body of experimental evidence has shown that impaired astrocytes play crucial roles in the pathologic process of cerebral ischemia; therefore, astrocytes may represent a breakthrough target for neuroprotective therapeutic strategies. Agmatine, an endogenous polyamine catalyzed from L-arginine by arginine decarboxylase (ADC), is a neuromodulator and it protects neurons/glia against various injuries.

Results: In this investigation, agmatine-producing mouse cortical astrocytes were developed through transduction of the human ADC gene. Cells were exposed to oxygen-glucose deprivation (OGD) and restored to a normoxic glucose-supplied condition. Intracellular levels of agmatine were measured by high performance liquid chromatography. Cell viability was evaluated by Hoechest/propidium iodide nuclear staining and lactate dehydrogenase assay. Expression of inducible nitric oxide synthase (iNOS) and matrix metalloproteinase s (MMPs) were assessed by a reverse transcription polymerase chain reaction, Western immunoblots, and immunofluorescence. We confirmed that ADC gene-expressed astrocytes produce a great amount of agmatine. These cells were highly resistant to not only OGD but also restoration, which mimicked ischemia-reperfusion injury in vivo. The neuroprotective effects of ADC seemed to be related to its ability to attenuate expression of iNOS and MMPs.

Conclusion: Our findings imply that astrocytes can be reinforced against oxidative stress by endogenous agmatine production through ADC gene transduction. The results of this study provide new insights that may lead to novel therapeutic approaches to reduce cerebral ischemic injuries.

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Related in: MedlinePlus

Immunofluorescence staining of human arginine decarboxylase (hADC)-introduced astrocytes after oxygen-glucose deprivation (OGD).(A, D, G) No treatment control astrocytes; (B, E, H) astrocytes after 4 hrs OGD; (C, F, I) hADC-astrocytes after 4 hrs OGD. Cells reacted to inducible nitric oxide synthase (iNOS) (A-C), matrix metalloproteinase (MMP) 2 (D-F), and MMP 9 (G-I) showed green fluorescence. Cells were counter-stained with astrocyte marker glial fibrillary acidic protein (GFAP; red fluorescence) and nuclear marker 4',6-diamidino-2-phenylindole (DAPI; blue fluorescence). Scale bar = 50 μm.
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Fig6: Immunofluorescence staining of human arginine decarboxylase (hADC)-introduced astrocytes after oxygen-glucose deprivation (OGD).(A, D, G) No treatment control astrocytes; (B, E, H) astrocytes after 4 hrs OGD; (C, F, I) hADC-astrocytes after 4 hrs OGD. Cells reacted to inducible nitric oxide synthase (iNOS) (A-C), matrix metalloproteinase (MMP) 2 (D-F), and MMP 9 (G-I) showed green fluorescence. Cells were counter-stained with astrocyte marker glial fibrillary acidic protein (GFAP; red fluorescence) and nuclear marker 4',6-diamidino-2-phenylindole (DAPI; blue fluorescence). Scale bar = 50 μm.

Mentions: Naive astrocytes seldom expressed iNOS and MMP-2/9 (Figure 6A,D,G). After 4 hrs of OGD, control astrocytes exhibited expression of iNOS and MMP-2/9 (Figure 6B, E, H); however, hADC-astrocytes did not show immunoreactivity to either iNOS or MMP-2/9 (Figure 6C, F, I).Figure 6


Retroviral expression of human arginine decarboxylase reduces oxidative stress injury in mouse cortical astrocytes.

Hong S, Son MR, Yun K, Lee WT, Park KA, Lee JE - BMC Neurosci (2014)

Immunofluorescence staining of human arginine decarboxylase (hADC)-introduced astrocytes after oxygen-glucose deprivation (OGD).(A, D, G) No treatment control astrocytes; (B, E, H) astrocytes after 4 hrs OGD; (C, F, I) hADC-astrocytes after 4 hrs OGD. Cells reacted to inducible nitric oxide synthase (iNOS) (A-C), matrix metalloproteinase (MMP) 2 (D-F), and MMP 9 (G-I) showed green fluorescence. Cells were counter-stained with astrocyte marker glial fibrillary acidic protein (GFAP; red fluorescence) and nuclear marker 4',6-diamidino-2-phenylindole (DAPI; blue fluorescence). Scale bar = 50 μm.
© Copyright Policy - open-access
Related In: Results  -  Collection

License 1 - License 2
Show All Figures
getmorefigures.php?uid=PMC4150973&req=5

Fig6: Immunofluorescence staining of human arginine decarboxylase (hADC)-introduced astrocytes after oxygen-glucose deprivation (OGD).(A, D, G) No treatment control astrocytes; (B, E, H) astrocytes after 4 hrs OGD; (C, F, I) hADC-astrocytes after 4 hrs OGD. Cells reacted to inducible nitric oxide synthase (iNOS) (A-C), matrix metalloproteinase (MMP) 2 (D-F), and MMP 9 (G-I) showed green fluorescence. Cells were counter-stained with astrocyte marker glial fibrillary acidic protein (GFAP; red fluorescence) and nuclear marker 4',6-diamidino-2-phenylindole (DAPI; blue fluorescence). Scale bar = 50 μm.
Mentions: Naive astrocytes seldom expressed iNOS and MMP-2/9 (Figure 6A,D,G). After 4 hrs of OGD, control astrocytes exhibited expression of iNOS and MMP-2/9 (Figure 6B, E, H); however, hADC-astrocytes did not show immunoreactivity to either iNOS or MMP-2/9 (Figure 6C, F, I).Figure 6

Bottom Line: The neuroprotective effects of ADC seemed to be related to its ability to attenuate expression of iNOS and MMPs.Our findings imply that astrocytes can be reinforced against oxidative stress by endogenous agmatine production through ADC gene transduction.The results of this study provide new insights that may lead to novel therapeutic approaches to reduce cerebral ischemic injuries.

View Article: PubMed Central - PubMed

Affiliation: Brain Korea 21 Project for Medical Science, and Brain Research Institute, Department of Anatomy, Yonsei University College of Medicine, 50 Yonsei-ro, Seodaemun-gu, Seoul 120-752, Republic of Korea. jelee@yuhs.ac.

ABSTRACT

Background: In physiologic and pathologic conditions of the central nervous system (CNS), astrocytes are a double-edged sword. They not only support neuronal homeostasis but also contribute to increases in neuronal demise. A large body of experimental evidence has shown that impaired astrocytes play crucial roles in the pathologic process of cerebral ischemia; therefore, astrocytes may represent a breakthrough target for neuroprotective therapeutic strategies. Agmatine, an endogenous polyamine catalyzed from L-arginine by arginine decarboxylase (ADC), is a neuromodulator and it protects neurons/glia against various injuries.

Results: In this investigation, agmatine-producing mouse cortical astrocytes were developed through transduction of the human ADC gene. Cells were exposed to oxygen-glucose deprivation (OGD) and restored to a normoxic glucose-supplied condition. Intracellular levels of agmatine were measured by high performance liquid chromatography. Cell viability was evaluated by Hoechest/propidium iodide nuclear staining and lactate dehydrogenase assay. Expression of inducible nitric oxide synthase (iNOS) and matrix metalloproteinase s (MMPs) were assessed by a reverse transcription polymerase chain reaction, Western immunoblots, and immunofluorescence. We confirmed that ADC gene-expressed astrocytes produce a great amount of agmatine. These cells were highly resistant to not only OGD but also restoration, which mimicked ischemia-reperfusion injury in vivo. The neuroprotective effects of ADC seemed to be related to its ability to attenuate expression of iNOS and MMPs.

Conclusion: Our findings imply that astrocytes can be reinforced against oxidative stress by endogenous agmatine production through ADC gene transduction. The results of this study provide new insights that may lead to novel therapeutic approaches to reduce cerebral ischemic injuries.

Show MeSH
Related in: MedlinePlus