RIT2 Gene’s Promise in Halting Parkinson’s Disease Progression Neuroscience News ... read more
Source: Google NewsPublished on 2023-05-25
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- The road ahead: 2022 January 20, 2022 # # # # The first post at the start of each year on the SoPD website tries to provide an overview of where things are in the search for ‘disease modifying’ therapies for Parkinson’s. It is an exercise in managing expectations as well as discussing what research events are scheduled for the next year so that we can keep…
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- The road ahead: 2020 January 5, 2020 Here at the SoPD, we are primarily interested in disease modification for Parkinson’s. While there is a great deal of interesting research exploring the causes of the condition, novel symptomatic therapies, and other aspects of Parkinson’s, my focus is generally on the science seeking to slow, stop or reverse the condition. At the start of each year, it is a…
- Rit2 silencing in dopamine neurons drives a progressive Parkinsonian phenotype May 10, 2023 bioRxiv. 2023 Apr 28:2023.04.26.538430. doi: 10.1101/2023.04.26.538430. Preprint.ABSTRACTParkinson's disease (PD) is the second most prevalent neurodegenerative disease and arises from dopamine (DA) neuron death selectively in the substantia nigra pars compacta (SNc) . Rit2 is a reported PD risk allele, and recent single cell transcriptomic studies identified a major RIT2 cluster in PD DA neurons, potentially linking Rit2 expression anomalies to…
- Rit2 silencing in dopamine neurons drives a progressive Parkinsonian phenotype May 10, 2023 bioRxiv. 2023 Apr 28:2023.04.26.538430. doi: 10.1101/2023.04.26.538430. Preprint.ABSTRACTParkinson's disease (PD) is the second most prevalent neurodegenerative disease and arises from dopamine (DA) neuron death selectively in the substantia nigra pars compacta (SNc) . Rit2 is a reported PD risk allele, and recent single cell transcriptomic studies identified a major RIT2 cluster in PD DA neurons, potentially linking Rit2 expression anomalies to…
- Rit2 silencing in dopamine neurons drives a progressive Parkinsonian phenotype May 10, 2023 bioRxiv. 2023 Apr 28:2023.04.26.538430. doi: 10.1101/2023.04.26.538430. Preprint.ABSTRACTParkinson's disease (PD) is the second most prevalent neurodegenerative disease and arises from dopamine (DA) neuron death selectively in the substantia nigra pars compacta (SNc) . Rit2 is a reported PD risk allele, and recent single cell transcriptomic studies identified a major RIT2 cluster in PD DA neurons, potentially linking Rit2 expression anomalies to…
- Rit2 silencing in dopamine neurons drives a progressive Parkinsonian phenotype May 10, 2023 bioRxiv. 2023 Apr 28:2023.04.26.538430. doi: 10.1101/2023.04.26.538430. Preprint.ABSTRACTParkinson's disease (PD) is the second most prevalent neurodegenerative disease and arises from dopamine (DA) neuron death selectively in the substantia nigra pars compacta (SNc) . Rit2 is a reported PD risk allele, and recent single cell transcriptomic studies identified a major RIT2 cluster in PD DA neurons, potentially linking Rit2 expression anomalies to…
- Rit2 silencing in dopamine neurons drives a progressive Parkinsonian phenotype May 10, 2023 bioRxiv. 2023 Apr 28:2023.04.26.538430. doi: 10.1101/2023.04.26.538430. Preprint.ABSTRACTParkinson's disease (PD) is the second most prevalent neurodegenerative disease and arises from dopamine (DA) neuron death selectively in the substantia nigra pars compacta (SNc) . Rit2 is a reported PD risk allele, and recent single cell transcriptomic studies identified a major RIT2 cluster in PD DA neurons, potentially linking Rit2 expression anomalies to…
- The small GTPase Rit2 modulates LRRK2 kinase activity, is required for lysosomal function and protects against alpha-synuclein neuropathology March 27, 2023 NPJ Parkinsons Dis. 2023 Mar 27;9(1):44. doi: 10.1038/s41531-023-00484-2.ABSTRACTIn Parkinson's disease (PD) misfolded alpha-synuclein (aSyn) accumulates in the substantia nigra, where dopaminergic neurons are progressively lost. The mechanisms underlying aSyn pathology are still unclear, but they are hypothesized to involve the autophagy-lysosome pathway (ALP). LRRK2 mutations are a major cause of familial and sporadic PD, and LRRK2 kinase activity has been…
- The small GTPase Rit2 modulates LRRK2 kinase activity, is required for lysosomal function and protects against alpha-synuclein neuropathology March 27, 2023 NPJ Parkinsons Dis. 2023 Mar 27;9(1):44. doi: 10.1038/s41531-023-00484-2.ABSTRACTIn Parkinson's disease (PD) misfolded alpha-synuclein (aSyn) accumulates in the substantia nigra, where dopaminergic neurons are progressively lost. The mechanisms underlying aSyn pathology are still unclear, but they are hypothesized to involve the autophagy-lysosome pathway (ALP). LRRK2 mutations are a major cause of familial and sporadic PD, and LRRK2 kinase activity has been…
- The small GTPase Rit2 modulates LRRK2 kinase activity, is required for lysosomal function and protects against alpha-synuclein neuropathology March 27, 2023 NPJ Parkinsons Dis. 2023 Mar 27;9(1):44. doi: 10.1038/s41531-023-00484-2.ABSTRACTIn Parkinson's disease (PD) misfolded alpha-synuclein (aSyn) accumulates in the substantia nigra, where dopaminergic neurons are progressively lost. The mechanisms underlying aSyn pathology are still unclear, but they are hypothesized to involve the autophagy-lysosome pathway (ALP). LRRK2 mutations are a major cause of familial and sporadic PD, and LRRK2 kinase activity has been…
- RIT2 Gene’s Promise in Halting Parkinson’s Disease Progression May 25, 2023 Researchers identified a protein that could play a significant role in preventing Parkinson's disease. The protein, linked to the RIT2 gene, is believed to control the accumulation of alpha-synuclein, which destroys neuronal cells and is a known indicator of the disease. Experiments conducted in cell models and on mice showed that increasing the expression of the RIT2 gene helped protect…
- A pH-eQTL Interaction at the RIT2-SYT4 Parkinson's Disease Risk Locus in the Substantia Nigra July 26, 2021 Front Aging Neurosci. 2021 Jul 9;13:690632. doi: 10.3389/fnagi.2021.690632. eCollection 2021.ABSTRACTParkinson's disease causes severe motor and cognitive disabilities that result from the progressive loss of dopamine neurons in the substantia nigra. The rs12456492 variant in the RIT2 gene has been repeatedly associated with increased risk for Parkinson's disease. From a transcriptomic perspective, a meta-analysis found that RIT2 gene expression is correlated…
- A pH-eQTL Interaction at the RIT2-SYT4 Parkinson's Disease Risk Locus in the Substantia Nigra July 26, 2021 Front Aging Neurosci. 2021 Jul 9;13:690632. doi: 10.3389/fnagi.2021.690632. eCollection 2021.ABSTRACTParkinson's disease causes severe motor and cognitive disabilities that result from the progressive loss of dopamine neurons in the substantia nigra. The rs12456492 variant in the RIT2 gene has been repeatedly associated with increased risk for Parkinson's disease. From a transcriptomic perspective, a meta-analysis found that RIT2 gene expression is correlated…
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