Eryptosis as a marker of Parkinson's disease
A major trend in recent Parkinson's disease (PD) research is the investigation of biological markers that could help in identifying at-risk individuals or to track disease progression and response to therapies. Central to this is the knowledge that inflammation is a known hallmark of PD and of...
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Veröffentlicht in: | Aging (Albany, NY.) NY.), 2014-10, Vol.6 (10), p.788-819 |
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creator | Pretorius, Etheresia Swanepoel, Albe C Buys, Antoinette V Vermeulen, Natasha Duim, Wiebren Kell, Douglas B |
description | A major trend in recent Parkinson's disease (PD) research is the investigation of biological markers that could help in identifying at-risk individuals or to track disease progression and response to therapies. Central to this is the knowledge that inflammation is a known hallmark of PD and of many other degenerative diseases. In the current work, we focus on inflammatory signalling in PD, using a systems approach that allows us to look at the disease in a more holistic way. We discuss cyclooxygenases, prostaglandins, thromboxanes and also iron in PD. These particular signalling molecules are involved in PD pathophysiology, but are also very important in an aberrant coagulation/hematology system. We present and discuss a hypothesis regarding the possible interaction of these aberrant signalling molecules implicated in PD, and suggest that these molecules may affect the erythrocytes of PD patients. This would be observable as changes in the morphology of the RBCs and of PD patients relative to healthy controls. We then show that the RBCs of PD patients are indeed rather dramatically deranged in their morphology, exhibiting eryptosis (a kind of programmed cell death). This morphological indicator may have useful diagnostic and prognostic significance. |
doi_str_mv | 10.18632/aging.100695 |
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This morphological indicator may have useful diagnostic and prognostic significance.</description><identifier>ISSN: 1945-4589</identifier><identifier>EISSN: 1945-4589</identifier><identifier>DOI: 10.18632/aging.100695</identifier><identifier>PMID: 25411230</identifier><language>eng</language><publisher>United States: Impact Journals LLC</publisher><subject>Aged ; Aged, 80 and over ; Biomarkers - blood ; Erythrocytes - pathology ; Female ; Ferritins - blood ; Humans ; Male ; Microscopy, Atomic Force ; Microscopy, Electron, Scanning ; Middle Aged ; Parkinson Disease - blood ; Parkinson Disease - pathology ; Research Paper</subject><ispartof>Aging (Albany, NY.), 2014-10, Vol.6 (10), p.788-819</ispartof><rights>Copyright: © 2014 Pretorius et al. 2014</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c387t-1e193b05e1f3c5d8055563d4a068e108ff67e9a99122cab9a3df1153107f9c63</citedby><cites>FETCH-LOGICAL-c387t-1e193b05e1f3c5d8055563d4a068e108ff67e9a99122cab9a3df1153107f9c63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4247384/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4247384/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25411230$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pretorius, Etheresia</creatorcontrib><creatorcontrib>Swanepoel, Albe C</creatorcontrib><creatorcontrib>Buys, Antoinette V</creatorcontrib><creatorcontrib>Vermeulen, Natasha</creatorcontrib><creatorcontrib>Duim, Wiebren</creatorcontrib><creatorcontrib>Kell, Douglas B</creatorcontrib><title>Eryptosis as a marker of Parkinson's disease</title><title>Aging (Albany, NY.)</title><addtitle>Aging (Albany NY)</addtitle><description>A major trend in recent Parkinson's disease (PD) research is the investigation of biological markers that could help in identifying at-risk individuals or to track disease progression and response to therapies. 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Central to this is the knowledge that inflammation is a known hallmark of PD and of many other degenerative diseases. In the current work, we focus on inflammatory signalling in PD, using a systems approach that allows us to look at the disease in a more holistic way. We discuss cyclooxygenases, prostaglandins, thromboxanes and also iron in PD. These particular signalling molecules are involved in PD pathophysiology, but are also very important in an aberrant coagulation/hematology system. We present and discuss a hypothesis regarding the possible interaction of these aberrant signalling molecules implicated in PD, and suggest that these molecules may affect the erythrocytes of PD patients. This would be observable as changes in the morphology of the RBCs and of PD patients relative to healthy controls. We then show that the RBCs of PD patients are indeed rather dramatically deranged in their morphology, exhibiting eryptosis (a kind of programmed cell death). This morphological indicator may have useful diagnostic and prognostic significance.</abstract><cop>United States</cop><pub>Impact Journals LLC</pub><pmid>25411230</pmid><doi>10.18632/aging.100695</doi><tpages>32</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Aged, 80 and over Biomarkers - blood Erythrocytes - pathology Female Ferritins - blood Humans Male Microscopy, Atomic Force Microscopy, Electron, Scanning Middle Aged Parkinson Disease - blood Parkinson Disease - pathology Research Paper |
title | Eryptosis as a marker of Parkinson's disease |
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