Plasmin deficiency leads to fibrin accumulation and a compromised inflammatory response in the mouse brain. (May 2014)
- Record Type:
- Journal Article
- Title:
- Plasmin deficiency leads to fibrin accumulation and a compromised inflammatory response in the mouse brain. (May 2014)
- Main Title:
- Plasmin deficiency leads to fibrin accumulation and a compromised inflammatory response in the mouse brain
- Authors:
- Hultman, K.
Cortes‐Canteli, M.
Bounoutas, A.
Richards, A. T.
Strickland, S.
Norris, E. H. - Abstract:
- <abstract abstract-type="main" id="jth12553-abs-0001"> <title>Summary</title> <sec id="jth12553-sec-0001" sec-type="section"> <title>Background</title> <p>Excess fibrin in blood vessels is cleared by plasmin, the key proteolytic enzyme in fibrinolysis. Neurological disorders and head trauma can result in the disruption of the neurovasculature and the entry of fibrin and other blood components into the brain, which may contribute to further neurological dysfunction.</p> </sec> <sec id="jth12553-sec-0002" sec-type="section"> <title>Objectives</title> <p>While chronic fibrin deposition is often implicated in neurological disorders, the pathological contributions attributable specifically to fibrin have been difficult to ascertain. An animal model that spontaneously acquires fibrin deposits could allow researchers to better understand the impact of fibrin in neurological disorders.</p> </sec> <sec id="jth12553-sec-0003" sec-type="section"> <title>Methods</title> <p>Brains of plasminogen <italic>(plg)‐</italic> and tissue plasminogen activator (<italic>tPA)‐</italic>deficient mice were examined and characterized with regard to fibrin accumulation, vascular and neuronal health, and inflammation. Furthermore, the inflammatory response following intrahippocampal lipopolysaccharide (LPS) injection was compared between <italic>plg</italic><sup>−/−</sup> and wild type (WT) mice.</p> </sec> <sec id="jth12553-sec-0004" sec-type="section"> <title>Results and Conclusions</title> <p>Both<abstract abstract-type="main" id="jth12553-abs-0001"> <title>Summary</title> <sec id="jth12553-sec-0001" sec-type="section"> <title>Background</title> <p>Excess fibrin in blood vessels is cleared by plasmin, the key proteolytic enzyme in fibrinolysis. Neurological disorders and head trauma can result in the disruption of the neurovasculature and the entry of fibrin and other blood components into the brain, which may contribute to further neurological dysfunction.</p> </sec> <sec id="jth12553-sec-0002" sec-type="section"> <title>Objectives</title> <p>While chronic fibrin deposition is often implicated in neurological disorders, the pathological contributions attributable specifically to fibrin have been difficult to ascertain. An animal model that spontaneously acquires fibrin deposits could allow researchers to better understand the impact of fibrin in neurological disorders.</p> </sec> <sec id="jth12553-sec-0003" sec-type="section"> <title>Methods</title> <p>Brains of plasminogen <italic>(plg)‐</italic> and tissue plasminogen activator (<italic>tPA)‐</italic>deficient mice were examined and characterized with regard to fibrin accumulation, vascular and neuronal health, and inflammation. Furthermore, the inflammatory response following intrahippocampal lipopolysaccharide (LPS) injection was compared between <italic>plg</italic><sup>−/−</sup> and wild type (WT) mice.</p> </sec> <sec id="jth12553-sec-0004" sec-type="section"> <title>Results and Conclusions</title> <p>Both <italic>plg</italic><sup>−/−</sup> and <italic>tPA</italic><sup>−/−</sup> mice exhibited brain parenchymal fibrin deposits that appear to result from reduced neurovascular integrity. Markers of neuronal health and inflammation were not significantly affected by proximity to the vascular lesions. A compromised neuroinflammatory response was also observed in <italic>plg</italic><sup>−/−</sup> compared to WT mice following intrahippocampal LPS injection. These results demonstrate that fibrin does not affect neuronal health in the absence of inflammation and suggest that plasmin may be necessary for a normal neuroinflammatory response in the mouse CNS.</p> </sec> </abstract> … (more)
- Is Part Of:
- Journal of thrombosis and haemostasis. Volume 12:Number 5(2014:May)
- Journal:
- Journal of thrombosis and haemostasis
- Issue:
- Volume 12:Number 5(2014:May)
- Issue Display:
- Volume 12, Issue 5 (2014)
- Year:
- 2014
- Volume:
- 12
- Issue:
- 5
- Issue Sort Value:
- 2014-0012-0005-0000
- Page Start:
- 701
- Page End:
- 712
- Publication Date:
- 2014-05
- Subjects:
- Thrombosis -- Periodicals
Hemostasis -- Periodicals
Blood coagulation disorders -- Periodicals
616.1 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1538-7836 ↗
http://www.blackwellpublishing.com/journals/jth ↗
https://www.sciencedirect.com/journal/journal-of-thrombosis-and-haemostasis ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/jth.12553 ↗
- Languages:
- English
- ISSNs:
- 1538-7933
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5069.345000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3003.xml