دورية أكاديمية

Does plasminogen activator inhibitor-1 drive lymphangiogenesis?

التفاصيل البيبلوغرافية
العنوان: Does plasminogen activator inhibitor-1 drive lymphangiogenesis?
المؤلفون: Bruyere, Francoise, Melen-Lamalle, Laurence, Blacher, Silvia, Detry, Benoît, Masset, Anne, Lecomte, Julie, Lambert, Vincent, Maillard, Catherine, Hoyer-Hansen, Gunilla, Lund, Leif R, Foidart, Jean-Michel, Noël, Agnès
المصدر: PLoS ONE, 5 (3), e9653 (2010)
بيانات النشر: Public Library of Science, 2010.
سنة النشر: 2010
مصطلحات موضوعية: Life sciences, Biochemistry, biophysics & molecular biology, Sciences du vivant, Biochimie, biophysique & biologie moléculaire
الوصف: The purpose of this study is to explore the function of plasminogen activator inhibitor-1 (PAI-1) during pathological lymphangiogenesis. PAI-1, the main physiological inhibitor of plasminogen activators is involved in pathological angiogenesis at least by controlling extracellular proteolysis and by regulating endothelial cell survival and migration. Protease system's role in lymphangiogenesis is unknown yet. Thus, based on its important pro-angiogenic effect, we hypothesized that PAI-1 may regulate lymphangiogenesis associated at least with metastatic dissemination of cancer cells. To address this issue, we studied the impact of PAI-1 deficiency in various murine models of tumoral lymphangiogenesis. Wild-type PAI-1 proficient mice were used as controls. We provide for the first time evidence that PAI-1 is dispensable for tumoral lymphangiogenesis associated with breast cancers either induced by mammary carcinoma cell injection or spontaneously appearing in transgenic mice expressing the polyomavirus middle T antigen (PymT) under the control of a mouse mammary tumor virus long-terminal repeat promoter (MMTV-LTR). We also investigated inflammation-related lymphatic vessel recruitment by using two inflammatory models. PAI-1 deficiency did neither affect the development of lymphangioma nor burn-induced corneal lymphangiogenesis. These novel data suggest that vascular remodelling associated with lymphangiogenesis and angiogenesis involve different molecular determinants. PAI-1 does not appear as a potential therapeutic target to counteract pathological lymphangiogenesis.
نوع الوثيقة: journal article
http://purl.org/coar/resource_type/c_6501
article
اللغة: English
Relation: info:eu-repo/grantAgreement/EC/FP7/201279; urn:issn:1932-6203
DOI: 10.1371/journal.pone.0009653
URL الوصول: https://orbi.uliege.be/handle/2268/29627
حقوق: open access
http://purl.org/coar/access_right/c_abf2
info:eu-repo/semantics/openAccess
رقم الأكسشن: edsorb.29627
قاعدة البيانات: ORBi
الوصف
DOI:10.1371/journal.pone.0009653