Plasma fibronectin supports neuronal survival and reduces brain injury following transient focal cerebral ischemia but is not essential for skin-wound healing and hemostasis
(2001) In Nature Medicine 7(3). p.324-330- Abstract
- Fibronectin performs essential roles in embryonic development and is prominently expressed during tissue repair. Two forms of fibronectin have been Identified: plasma fibronectin (pFn), which Is expressed by hepatocytes and secreted In soluble form into plasma; and cellular fibronectin (cFn), an insoluble form expressed locally by fibroblasts and other cell types and deposited and assembled into the extracellular matrix. To investigate the role of pFn in vivo, we generated pfn-deficient adult mice using Cre-loxP conditional gene-knockout technology. Here we show that pfn-deficient mice show increased neuronal apoptosis and larger Infarction areas following transient focal cerebral ischemia. However, pFn is dispensable for skin-wound... (More)
- Fibronectin performs essential roles in embryonic development and is prominently expressed during tissue repair. Two forms of fibronectin have been Identified: plasma fibronectin (pFn), which Is expressed by hepatocytes and secreted In soluble form into plasma; and cellular fibronectin (cFn), an insoluble form expressed locally by fibroblasts and other cell types and deposited and assembled into the extracellular matrix. To investigate the role of pFn in vivo, we generated pfn-deficient adult mice using Cre-loxP conditional gene-knockout technology. Here we show that pfn-deficient mice show increased neuronal apoptosis and larger Infarction areas following transient focal cerebral ischemia. However, pFn is dispensable for skin-wound healing and hemostasis. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/1119495
- author
- Sakai, Takao LU ; Johnson, Kamin J. ; Murozono, Michihiro ; Sakai, Keiko LU ; Magnuson, Marc A. ; Wieloch, Tadeusz LU ; Cronberg, Tobias LU ; Isshiki, Atsushi ; Erickson, Harold P. and Fässler, Reinhard LU
- organization
- publishing date
- 2001
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Nature Medicine
- volume
- 7
- issue
- 3
- pages
- 324 - 330
- publisher
- Nature Publishing Group
- external identifiers
-
- wos:000167380400038
- scopus:0035099411
- ISSN
- 1546-170X
- DOI
- 10.1038/85471
- language
- English
- LU publication?
- yes
- additional info
- The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Laboratory for Experimental Brain Research (013041000), Department of Clinical Sciences, Lund (013230000)
- id
- 6ab34973-d933-4e4a-8f99-5f317477e471 (old id 1119495)
- date added to LUP
- 2016-04-01 15:25:58
- date last changed
- 2022-03-14 18:11:27
@article{6ab34973-d933-4e4a-8f99-5f317477e471, abstract = {{Fibronectin performs essential roles in embryonic development and is prominently expressed during tissue repair. Two forms of fibronectin have been Identified: plasma fibronectin (pFn), which Is expressed by hepatocytes and secreted In soluble form into plasma; and cellular fibronectin (cFn), an insoluble form expressed locally by fibroblasts and other cell types and deposited and assembled into the extracellular matrix. To investigate the role of pFn in vivo, we generated pfn-deficient adult mice using Cre-loxP conditional gene-knockout technology. Here we show that pfn-deficient mice show increased neuronal apoptosis and larger Infarction areas following transient focal cerebral ischemia. However, pFn is dispensable for skin-wound healing and hemostasis.}}, author = {{Sakai, Takao and Johnson, Kamin J. and Murozono, Michihiro and Sakai, Keiko and Magnuson, Marc A. and Wieloch, Tadeusz and Cronberg, Tobias and Isshiki, Atsushi and Erickson, Harold P. and Fässler, Reinhard}}, issn = {{1546-170X}}, language = {{eng}}, number = {{3}}, pages = {{324--330}}, publisher = {{Nature Publishing Group}}, series = {{Nature Medicine}}, title = {{Plasma fibronectin supports neuronal survival and reduces brain injury following transient focal cerebral ischemia but is not essential for skin-wound healing and hemostasis}}, url = {{http://dx.doi.org/10.1038/85471}}, doi = {{10.1038/85471}}, volume = {{7}}, year = {{2001}}, }