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Altered expression of angiogenesis and lymphangiogenesis markers in the uninvolved skin of plaque‐type psoriasis

Identifieur interne : 006210 ( Istex/Corpus ); précédent : 006209; suivant : 006211

Altered expression of angiogenesis and lymphangiogenesis markers in the uninvolved skin of plaque‐type psoriasis

Auteurs : A. Henno ; S. Blacher ; C. Lambert ; A. Colige ; L. Seidel ; A. Noël ; C. Lapière ; M. De La Brassinne ; B. V. Nusgens

Source :

RBID : ISTEX:D0D5499369704D67EFC5B6C1BA570626DA2364CF

Abstract

Background  Vascular alterations are significant events in the pathomechanism of psoriasis. A disorder in the mechanisms regulating skin angiogenesis and lymphangiogenesis could participate in the pathogenesis of the disease.

Url:
DOI: 10.1111/j.1365-2133.2008.08889.x

Links to Exploration step

ISTEX:D0D5499369704D67EFC5B6C1BA570626DA2364CF

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<hi rend="bold">Background </hi>
Vascular alterations are significant events in the pathomechanism of psoriasis. A disorder in the mechanisms regulating skin angiogenesis and lymphangiogenesis could participate in the pathogenesis of the disease.</p>
<p>
<hi rend="bold">Objectives </hi>
To quantify differences in the expression of angiogenesis and lymphangiogenesis growth factors, receptors, coreceptors as well as their antagonists in the uninvolved skin of patients with psoriasis compared with the skin of nonpsoriatic volunteers.</p>
<p>
<hi rend="bold">Methods </hi>
Skin biopsies were collected from the involved skin of 13 patients with untreated plaque‐type psoriasis, from their nonlesional skin at distance from the lesions and from the skin of 16 healthy volunteers. The mRNA steady‐state level of keratins 10, 14 and 16, glyceraldehyde‐3‐phosphate dehydrogenase (GAPDH), vimentin, collagen I and IV, proliferating cell nuclear antigen, the various splice variants of vascular endothelial growth factor, VEGF‐A, VEGF‐C and VEGF‐D, their receptors VEGFR1, VEGFR2 and VEGFR3, neuropilin (NRP)‐1 and its soluble forms, NRP‐2, semaphorin 3A and prox‐1, was measured by reverse transcription–polymerase chain reaction. Immunohistochemistry was performed for Ki‐67, von Willebrand factor and D2‐40. Blood and lymphatic vessel density, area and distance from epidermis were estimated by morphological analysis coupled to an original computer‐assisted method of quantification.</p>
<p>
<hi rend="bold">Results </hi>
Skin from healthy volunteers and nonlesional skin from patients with psoriasis displayed similar histological, morphometric and proliferative features. However, a significant overexpression of VEGFR3, the VEGF‐A isoform VEGF121, soluble 12 NRP‐1 and GAPDH was observed in the nonlesional psoriatic skin as compared with that of normal volunteers.</p>
<p>
<hi rend="bold">Conclusions </hi>
These data point to significant differences in the blood and lymphatic vascular transcriptome between the clinically normal‐appearing skin of patients with psoriasis and the skin of volunteers without psoriasis.</p>
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<doi origin="wiley" registered="yes">10.1111/(ISSN)1365-2133</doi>
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<title type="main" sort="BRITISH JOURNAL OF DERMATOLOGY">British Journal of Dermatology</title>
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<doi origin="wiley">10.1111/bjd.2009.160.issue-3</doi>
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<numbering type="journalVolume" number="160">160</numbering>
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<coverDate startDate="2009-03">March 2009</coverDate>
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<doi origin="wiley">10.1111/j.1365-2133.2008.08889.x</doi>
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<title type="tocHeading1">Original articles</title>
<title type="tocHeading2">Dermatopathology</title>
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<copyright>© 2008 The Authors. Journal Compilation © 2008 British Association of Dermatologists</copyright>
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<correspondenceTo>Audrey Henno.
E‐mail:
<email>audrey.henno@student.ulg.ac.be</email>
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<title type="main">Altered expression of angiogenesis and lymphangiogenesis markers in the uninvolved skin of plaque‐type psoriasis</title>
<title type="shortAuthors">A. Henno
<i>et al.</i>
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<title type="short">Vascular markers in uninvolved psoriatic skin</title>
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<familyName>Noël</familyName>
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<personName>
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<familyName>Lapière</familyName>
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<familyName>De La Brassinne</familyName>
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<unparsedAffiliation>Department of Dermatology</unparsedAffiliation>
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<unparsedAffiliation>Laboratory of Connective Tissues Biology, GIGA‐R</unparsedAffiliation>
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<unparsedAffiliation>Department of Biostatistics, University Hospital of Liège, University of Liège, B23, 4000 Liège, Belgium</unparsedAffiliation>
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<keyword xml:id="k1">angiogenesis</keyword>
<keyword xml:id="k2">lymphangiogenesis</keyword>
<keyword xml:id="k3">psoriasis</keyword>
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<title type="main">Summary</title>
<p>
<b>Background </b>
Vascular alterations are significant events in the pathomechanism of psoriasis. A disorder in the mechanisms regulating skin angiogenesis and lymphangiogenesis could participate in the pathogenesis of the disease.</p>
<p>
<b>Objectives </b>
To quantify differences in the expression of angiogenesis and lymphangiogenesis growth factors, receptors, coreceptors as well as their antagonists in the uninvolved skin of patients with psoriasis compared with the skin of nonpsoriatic volunteers.</p>
<p>
<b>Methods </b>
Skin biopsies were collected from the involved skin of 13 patients with untreated plaque‐type psoriasis, from their nonlesional skin at distance from the lesions and from the skin of 16 healthy volunteers. The mRNA steady‐state level of keratins 10, 14 and 16, glyceraldehyde‐3‐phosphate dehydrogenase (GAPDH), vimentin, collagen I and IV, proliferating cell nuclear antigen, the various splice variants of vascular endothelial growth factor, VEGF‐A, VEGF‐C and VEGF‐D, their receptors VEGFR1, VEGFR2 and VEGFR3, neuropilin (NRP)‐1 and its soluble forms, NRP‐2, semaphorin 3A and prox‐1, was measured by reverse transcription–polymerase chain reaction. Immunohistochemistry was performed for Ki‐67, von Willebrand factor and D2‐40. Blood and lymphatic vessel density, area and distance from epidermis were estimated by morphological analysis coupled to an original computer‐assisted method of quantification.</p>
<p>
<b>Results </b>
Skin from healthy volunteers and nonlesional skin from patients with psoriasis displayed similar histological, morphometric and proliferative features. However, a significant overexpression of VEGFR3, the VEGF‐A isoform VEGF121, soluble 12 NRP‐1 and GAPDH was observed in the nonlesional psoriatic skin as compared with that of normal volunteers.</p>
<p>
<b>Conclusions </b>
These data point to significant differences in the blood and lymphatic vascular transcriptome between the clinically normal‐appearing skin of patients with psoriasis and the skin of volunteers without psoriasis.</p>
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<p>Conflicts of interest
None declared.</p>
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<p>Part of this work has been presented in abstract form at the 36th European Society of Dermatological Research meeting held in Paris, 7–9 September 2006.</p>
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<abstract>Background  Vascular alterations are significant events in the pathomechanism of psoriasis. A disorder in the mechanisms regulating skin angiogenesis and lymphangiogenesis could participate in the pathogenesis of the disease.</abstract>
<abstract>Objectives  To quantify differences in the expression of angiogenesis and lymphangiogenesis growth factors, receptors, coreceptors as well as their antagonists in the uninvolved skin of patients with psoriasis compared with the skin of nonpsoriatic volunteers.</abstract>
<abstract>Methods  Skin biopsies were collected from the involved skin of 13 patients with untreated plaque‐type psoriasis, from their nonlesional skin at distance from the lesions and from the skin of 16 healthy volunteers. The mRNA steady‐state level of keratins 10, 14 and 16, glyceraldehyde‐3‐phosphate dehydrogenase (GAPDH), vimentin, collagen I and IV, proliferating cell nuclear antigen, the various splice variants of vascular endothelial growth factor, VEGF‐A, VEGF‐C and VEGF‐D, their receptors VEGFR1, VEGFR2 and VEGFR3, neuropilin (NRP)‐1 and its soluble forms, NRP‐2, semaphorin 3A and prox‐1, was measured by reverse transcription–polymerase chain reaction. Immunohistochemistry was performed for Ki‐67, von Willebrand factor and D2‐40. Blood and lymphatic vessel density, area and distance from epidermis were estimated by morphological analysis coupled to an original computer‐assisted method of quantification.</abstract>
<abstract>Results  Skin from healthy volunteers and nonlesional skin from patients with psoriasis displayed similar histological, morphometric and proliferative features. However, a significant overexpression of VEGFR3, the VEGF‐A isoform VEGF121, soluble 12 NRP‐1 and GAPDH was observed in the nonlesional psoriatic skin as compared with that of normal volunteers.</abstract>
<abstract>Conclusions  These data point to significant differences in the blood and lymphatic vascular transcriptome between the clinically normal‐appearing skin of patients with psoriasis and the skin of volunteers without psoriasis.</abstract>
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