Filip Braet

Dr. Filip Braet

School of Medical Sciences, The University of Sydney, Sydney, New South Wales, Australia
orcid

Research Focus & Metrics

Academic Career Length

33Years (1994-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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10 March 2010 in Angewandte Chemie International Edition
Verified
Journal Article
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WYWenrong Yang
Wenrong Yang
KRKyle R. Ratinac
Kyle R. Ratinac
SRSimon P. Ringer
Simon P. Ringer
PTPall Thordarson
Pall Thordarson
J. GoodingJ. Gooding
J. Gooding
Filip BraetFilip Braet
Filip Braet

23 August 2002 in Comparative Hepatology
Verified
Journal Article
Open access
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Filip BraetFilip Braet
Filip Braet
EWEddie Wisse
Eddie Wisse
This review provides a detailed overview of the current state of knowledge about the ultrastructure and dynamics of liver sinusoidal endothelial fenestrae. Various aspects of liver sinusoidal endothelial fenestrae regarding their structure, origin, species specificity, dynamics and formation will be explored. In addition, the role of liver sinusoidal endothelial fenestrae in relation to lipoprotein metabolism, fibrosis and cancer will be approached.

12 September 2007 in Nanotechnology
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Journal Article
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WYWenrong Yang
Wenrong Yang
PTPall Thordarson
Pall Thordarson
J. GoodingJ. Gooding
J. Gooding
SRSimon P Ringer
Simon P Ringer
Filip BraetFilip Braet
Filip Braet

1 May 2009 in American Journal of Physiology-Renal Physiology
Verified
Journal Article
Open access
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SSSimon C. Satchell
Simon C. Satchell
Filip BraetFilip Braet
Filip Braet
Glomerular endothelial cell (GEnC) fenestrations are analogous to podocyte filtration slits, but their important contribution to the glomerular filtration barrier has not received corresponding attention. GEnC fenestrations are transcytoplasmic holes, specialized for their unique role as a prerequisite for filtration across the glomerular capillary wall. Glomerular filtration rate is dependent on the fractional area of the fenestrations and, through the glycocalyx they contain, GEnC fenestrations are important in restriction of protein passage. Hence, dysregulation of GEnC fenestrations may be associated with both renal failure and proteinuria, and the pathophysiological importance of GEnC fenestrations is well characterized in conditions such as preeclampsia. Recent evidence suggests a wider significance in repair of glomerular injury and in common, yet serious, conditions, including diabetic nephropathy. Study of endothelial cell fenestrations is challenging because of limited availability of suitable in vitro models and by the requirement for electron microscopy to image these sub-100-nm structures. However, extensive evidence, from glomerular development in rodents to in vitro studies in human GEnC, points to vascular endothelial growth factor (VEGF) as a key inducer of fenestrations. In systemic endothelial fenestrations, the intracellular pathways through which VEGF acts to induce fenestrations include a key role for the fenestral diaphragm protein plasmalemmal vesicle-associated protein-1 (PV-1). The role of PV-1 in GEnC is less clear, not least because of controversy over existence of GEnC fenestral diaphragms. In this article, the structure-function relationships of GEnC fenestrations will be evaluated in depth, their role in health and disease explored, and the outlook for future study and therapeutic implications of these peculiar structures will be approached.

30 September 1999 in Microscopy Research and Technique
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Journal Article
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ISIlan Spector
Ilan Spector
Filip BraetFilip Braet
Filip Braet
NSNava R. Shochet
Nava R. Shochet
MBMichael R. Bubb
Michael R. Bubb

1 April 1997 in Journal of Microscopy
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Journal Article
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Filip BraetFilip Braet
Filip Braet
RZR. De Zanger
R. De Zanger
EWE. Wisse
E. Wisse