Blast‐Overpressure Induced Modulation of PARP‐SIRT‐NRF2 Axis in Stress Signaling of Astrocytes and Microglia
ABSTRACT Background The pathomechanism of blast traumatic brain injury (TBI) and blunt TBI is different. In blast injury, evidence indicates that a single blast exposure can often manifest long‐term neurological impairments. However, its pathomechanism is still elusive, and treatments have been symp...
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Wiley
2025-01-01
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| Series: | Immunity, Inflammation and Disease |
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| Online Access: | https://doi.org/10.1002/iid3.70106 |
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| author | Vijaya Prakash Krishnan Muthaiah Kathiravan Kaliyappan Ramkumar Thiayagarajan Supriya Mahajan Krishnamoorthy Gunasekaran |
| author_facet | Vijaya Prakash Krishnan Muthaiah Kathiravan Kaliyappan Ramkumar Thiayagarajan Supriya Mahajan Krishnamoorthy Gunasekaran |
| author_sort | Vijaya Prakash Krishnan Muthaiah |
| collection | DOAJ |
| description | ABSTRACT Background The pathomechanism of blast traumatic brain injury (TBI) and blunt TBI is different. In blast injury, evidence indicates that a single blast exposure can often manifest long‐term neurological impairments. However, its pathomechanism is still elusive, and treatments have been symptomatic. Poly adenosine diphosphate (ADP) ribose polymerase‐1 (PARP1) is implicated in the parthanatos and secondary neuroinflammation. Animal studies indicate the over‐activation of PARP1 as a significant downstream event underlying the neurological sequelae of several traumatic and neurodegenerative disorders, irrespective of the mode of cell death. PARP over‐activation forms ADP polymers on several nuclear proteins, known as trans‐PARylation, by consuming nicotinamide adenine dinucleotide (NAD+) and ATP. As NAD+ is a substrate for sirtuins, ithas also been implicated in the oxidative stress underlying TBI pathology. Hypothesis We recently established the implication of PARP1 following blast overpressure (BOP) and its differential response on astrocytes and microglial cells. We found that the inhibition of PARP is proven beneficial by attenuating oxidative stress. In this study, we hypothesized the involvement of the PARP1‐SIRT‐NRF2 axis following induced blast‐induced PARP over‐activation in glial cells for the manifestation of oxidative stress in BOP insults. Objective The objective is to determine the downstream modulation of the PARP‐SIRT‐NRF2 axis and changes in ATP levels following blast exposure in astrocytes and microglia cell lines. Results As a result of NAD+ being a common substrate for PARP1 and Sirtuins, we found the decreased expression of SIRT1, SIRT3, and NRF2, a central transcriptional regulator for the expression of antioxidant genes. We found that ATP levels were elevated post‐BOP from both glycolysis and oxidative phosphorylation (OXPHOS), an increase of ATP by glycolysis more significant than OXPHOS source, indicating the proinflammation post‐BOP. Conclusion This result shows that blast‐induced PARP1 over‐activation impacts the deacetylation activity of sirtuins and consequently impacts the regulation of antioxidant levels in astrocytes and microglia. |
| format | Article |
| id | doaj-art-4c890df81b9b4ba995081e08d73d2f7f |
| institution | Kabale University |
| issn | 2050-4527 |
| language | English |
| publishDate | 2025-01-01 |
| publisher | Wiley |
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| series | Immunity, Inflammation and Disease |
| spelling | doaj-art-4c890df81b9b4ba995081e08d73d2f7f2025-02-06T07:50:38ZengWileyImmunity, Inflammation and Disease2050-45272025-01-01131n/an/a10.1002/iid3.70106Blast‐Overpressure Induced Modulation of PARP‐SIRT‐NRF2 Axis in Stress Signaling of Astrocytes and MicrogliaVijaya Prakash Krishnan Muthaiah0Kathiravan Kaliyappan1Ramkumar Thiayagarajan2Supriya Mahajan3Krishnamoorthy Gunasekaran4Department of Rehabilitation Sciences, School of Public Health and Health Professions University at Buffalo Buffalo New York USADepartment of Rehabilitation Sciences, School of Public Health and Health Professions University at Buffalo Buffalo New York USADepartment of Geriatric Medicine, Kansas University Medical Center The University of Kansas Kansas City Kansas USADepartment of Medicine, Division of Allergy, Immunology & Rheumatology SUNY University at Buffalo Buffalo New York USADepartment of Medical Biochemistry, Institute of Health Dambi Dollo University Dambi Dolo EthiopiaABSTRACT Background The pathomechanism of blast traumatic brain injury (TBI) and blunt TBI is different. In blast injury, evidence indicates that a single blast exposure can often manifest long‐term neurological impairments. However, its pathomechanism is still elusive, and treatments have been symptomatic. Poly adenosine diphosphate (ADP) ribose polymerase‐1 (PARP1) is implicated in the parthanatos and secondary neuroinflammation. Animal studies indicate the over‐activation of PARP1 as a significant downstream event underlying the neurological sequelae of several traumatic and neurodegenerative disorders, irrespective of the mode of cell death. PARP over‐activation forms ADP polymers on several nuclear proteins, known as trans‐PARylation, by consuming nicotinamide adenine dinucleotide (NAD+) and ATP. As NAD+ is a substrate for sirtuins, ithas also been implicated in the oxidative stress underlying TBI pathology. Hypothesis We recently established the implication of PARP1 following blast overpressure (BOP) and its differential response on astrocytes and microglial cells. We found that the inhibition of PARP is proven beneficial by attenuating oxidative stress. In this study, we hypothesized the involvement of the PARP1‐SIRT‐NRF2 axis following induced blast‐induced PARP over‐activation in glial cells for the manifestation of oxidative stress in BOP insults. Objective The objective is to determine the downstream modulation of the PARP‐SIRT‐NRF2 axis and changes in ATP levels following blast exposure in astrocytes and microglia cell lines. Results As a result of NAD+ being a common substrate for PARP1 and Sirtuins, we found the decreased expression of SIRT1, SIRT3, and NRF2, a central transcriptional regulator for the expression of antioxidant genes. We found that ATP levels were elevated post‐BOP from both glycolysis and oxidative phosphorylation (OXPHOS), an increase of ATP by glycolysis more significant than OXPHOS source, indicating the proinflammation post‐BOP. Conclusion This result shows that blast‐induced PARP1 over‐activation impacts the deacetylation activity of sirtuins and consequently impacts the regulation of antioxidant levels in astrocytes and microglia.https://doi.org/10.1002/iid3.70106ATPblast‐overpressureGliapoly ADP‐ribose polymerasesirtuins |
| spellingShingle | Vijaya Prakash Krishnan Muthaiah Kathiravan Kaliyappan Ramkumar Thiayagarajan Supriya Mahajan Krishnamoorthy Gunasekaran Blast‐Overpressure Induced Modulation of PARP‐SIRT‐NRF2 Axis in Stress Signaling of Astrocytes and Microglia Immunity, Inflammation and Disease ATP blast‐overpressure Glia poly ADP‐ribose polymerase sirtuins |
| title | Blast‐Overpressure Induced Modulation of PARP‐SIRT‐NRF2 Axis in Stress Signaling of Astrocytes and Microglia |
| title_full | Blast‐Overpressure Induced Modulation of PARP‐SIRT‐NRF2 Axis in Stress Signaling of Astrocytes and Microglia |
| title_fullStr | Blast‐Overpressure Induced Modulation of PARP‐SIRT‐NRF2 Axis in Stress Signaling of Astrocytes and Microglia |
| title_full_unstemmed | Blast‐Overpressure Induced Modulation of PARP‐SIRT‐NRF2 Axis in Stress Signaling of Astrocytes and Microglia |
| title_short | Blast‐Overpressure Induced Modulation of PARP‐SIRT‐NRF2 Axis in Stress Signaling of Astrocytes and Microglia |
| title_sort | blast overpressure induced modulation of parp sirt nrf2 axis in stress signaling of astrocytes and microglia |
| topic | ATP blast‐overpressure Glia poly ADP‐ribose polymerase sirtuins |
| url | https://doi.org/10.1002/iid3.70106 |
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