ÿþ<HTML><HEAD><TITLE>25º Congresso Brasileiro de Microbiologia </TITLE><link rel=STYLESHEET type=text/css href=css.css></HEAD><BODY aLink=#ff0000 bgColor=#FFFFFF leftMargin=0 link=#000000 text=#000000 topMargin=0 vLink=#000000 marginheight=0 marginwidth=0><table align=center width=700 cellpadding=0 cellspacing=0><tr><td align=left bgcolor=#cccccc valign=top width=550><font face=arial size=2><strong><font face=Verdana, Arial, Helvetica, sans-serif size=3><font size=1>25º Congresso Brasileiro de Microbiologia </font></font></strong><font face=Verdana size=1><b><br></b></font><font face=Verdana, Arial,Helvetica, sans-serif size=1><strong> </strong></font></font></td><td align=right bgcolor=#cccccc valign=top width=150><font face=arial size=2><strong><font face=Verdana, Arial, Helvetica, sans-serif size=1><font size=1>ResumoID:1120-1</font></em></font></strong></font></td></tr><tr><td colspan=2><br><br><table align=center width=700><tr><td>Área: <b>Imunologia ( Divisão E )</b><p align=justify><strong><P>MYCOBACTERIUM LEPRAE INDUCES MMP9 EXPRESSION AND ACTIVITY IN PBMC FROM LEPROSY PATIENTS</P></strong></p><p align=justify><b>Rosane Teles </b> (<i>FIOCRUZ</i>); <b>Rose Teles </b> (<i>FIOCRUZ</i>); <b><u>Thaís Amadeu </u></b> (<i>FIOCRUZ</i>); <b>Danielle Moura </b> (<i>FIOCRUZ</i>); <b>Leila Mendonça-lima </b> (<i>FIOCRUZ</i>); <b>José Nery </b> (<i>FIOCRUZ</i>); <b>Euzenir Sarno </b> (<i>FIOCRUZ</i>); <b>Elizabeth Sampaio </b> (<i>NIAID</i>)<br><br></p><b><font size=2>Resumo</font></b><p align=justify class=tres><font size=2><P class=MsoNormal style="MARGIN: 0cm 0cm 0pt; TEXT-ALIGN: justify; mso-layout-grid-align: none"><SPAN lang=EN-US style="mso-ansi-language: EN-US">Gelatinases A and B (MMP-2 and MMP-9) </SPAN><SPAN lang=EN-US style="mso-ansi-language: EN-US; mso-fareast-font-family: Arial">can induce basal membrane breakdown and leukocyte migration, but t</SPAN><SPAN lang=EN-US style="mso-ansi-language: EN-US">heir role in leprosy skin inflammation remains unclear. Considering the participation of MMPs in the disease</SPAN><SPAN lang=EN-US style="FONT-FAMILY: Times-Roman; mso-ansi-language: EN-US; mso-bidi-font-family: Times-Roman">, t</SPAN><SPAN lang=EN-US style="mso-ansi-language: EN-US">he aims of this study were: 1) to determine whether <I style="mso-bidi-font-style: normal">Mycobaterium leprae</I> (ML) is able to induce the production MMP-9; 2) to determine whether both pro- and active MMP-9 proteins can be detected in the <I style="mso-bidi-font-style: normal">M. leprae</I>-stimulated cultures; and 3) to investigate whether <I style="mso-bidi-font-style: normal">M. leprae</I> and TNF</SPAN><FONT face=Symbol>a</FONT><SPAN lang=EN-US style="mso-ansi-language: EN-US"> could drive MMP production <I style="mso-bidi-font-style: normal">in vitro</I>. For that, PBMCs from leprosy patients were stimulated <I style="mso-bidi-font-style: normal">in vitro</I> with ML<I style="mso-bidi-font-style: normal">,</I> TNF</SPAN><SPAN style="FONT-FAMILY: Symbol; mso-ascii-font-family: 'Times New Roman'; mso-hansi-font-family: 'Times New Roman'; mso-char-type: symbol; mso-symbol-font-family: Symbol"><SPAN style="mso-char-type: symbol; mso-symbol-font-family: Symbol">a</SPAN></SPAN><SPAN style="mso-ansi-language: EN-US"> <SPAN lang=EN-US>or ML + TNF</SPAN></SPAN><SPAN style="FONT-FAMILY: Symbol; mso-ascii-font-family: 'Times New Roman'; mso-hansi-font-family: 'Times New Roman'; mso-char-type: symbol; mso-symbol-font-family: Symbol"><SPAN style="mso-char-type: symbol; mso-symbol-font-family: Symbol">a</SPAN></SPAN><SPAN style="mso-ansi-language: EN-US"> <SPAN lang=EN-US>after different culture periods, and mRNA, protein expression and zymography were performed. By <I style="mso-bidi-font-style: normal">in vitro</I> stimulation of PBMCs, ML induced the expression of MMP-9 (mRNA and protein) from the cultured cells.</SPAN></SPAN><SPAN lang=EN-US style="mso-ansi-language: EN-US; mso-fareast-font-family: Arial"> </SPAN><SPAN lang=EN-US style="mso-ansi-language: EN-US">Data confirm the ability of ML to induce the expression of the active forms of MMP-9. Since TNF</SPAN><FONT face=Symbol>a</FONT><SPAN style="mso-ansi-language: EN-US"> <SPAN lang=EN-US>has been shown to promote MMP secretion, we&nbsp;investigated whether <I>M. leprae </I>and TNF</SPAN></SPAN><FONT face=Symbol>a</FONT><SPAN style="mso-ansi-language: EN-US"> <SPAN lang=EN-US>could drive MMP production <I style="mso-bidi-font-style: normal">in vitro</I>. MMP-9 mRNA was increased in the presence of TNF</SPAN></SPAN><SPAN style="FONT-FAMILY: Symbol; mso-ascii-font-family: 'Times New Roman'; mso-hansi-font-family: 'Times New Roman'; mso-char-type: symbol; mso-symbol-font-family: Symbol"><SPAN style="mso-char-type: symbol; mso-symbol-font-family: Symbol">a</SPAN></SPAN><SPAN lang=EN-US style="mso-ansi-language: EN-US"> (<I style="mso-bidi-font-style: normal">p</I>&lt;0.05) or ML (<I style="mso-bidi-font-style: normal">p</I>&lt;0.05), and ML+TNF</SPAN><SPAN style="FONT-FAMILY: Symbol; mso-ascii-font-family: 'Times New Roman'; mso-hansi-font-family: 'Times New Roman'; mso-char-type: symbol; mso-symbol-font-family: Symbol"><SPAN style="mso-char-type: symbol; mso-symbol-font-family: Symbol">a</SPAN></SPAN><SPAN lang=EN-US style="mso-ansi-language: EN-US"> (<I style="mso-bidi-font-style: normal">p</I>&lt;0.001) in comparison to control cells. In addition, the increase of MMP-9 mRNA was detected when ML+TNF</SPAN><SPAN style="FONT-FAMILY: Symbol; mso-ascii-font-family: 'Times New Roman'; mso-hansi-font-family: 'Times New Roman'; mso-char-type: symbol; mso-symbol-font-family: Symbol"><SPAN style="mso-char-type: symbol; mso-symbol-font-family: Symbol">a</SPAN></SPAN><SPAN lang=EN-US style="mso-ansi-language: EN-US"> stimulated cells were compared with<I style="mso-bidi-font-style: normal"> </I>ML- or TNF</SPAN><SPAN style="FONT-FAMILY: Symbol; mso-ascii-font-family: 'Times New Roman'; mso-hansi-font-family: 'Times New Roman'; mso-char-type: symbol; mso-symbol-font-family: Symbol"><SPAN style="mso-char-type: symbol; mso-symbol-font-family: Symbol">a</SPAN></SPAN><SPAN lang=EN-US style="mso-ansi-language: EN-US">-stimulated cultures (<I style="mso-bidi-font-style: normal">p&lt;</I>0.05). MMP-9 levels in culture supernatants induced by ML+TNF (mean = 64.5 ± 7.3ng/ml) were higher than those induced by ML (45 ± 8ng/ml). mRNA expression induced by ML+TNF, although slightly elevated in comparison to ML alone (<I style="mso-bidi-font-style: normal">p</I>&gt;0.05); protein levels were not altered by <I style="mso-bidi-font-style: normal">M. leprae</I> or TNF. </SPAN><SPAN lang=EN-US style="mso-ansi-language: EN-US; mso-fareast-font-family: Arial">Our results demonstrate that </SPAN><SPAN lang=EN-US style="mso-ansi-language: EN-US">ML induces MMP-9 expression and activity in PBMCs from leprosy patients and that <SPAN style="mso-bidi-font-weight: bold; mso-bidi-font-style: italic">TNF synergizes with <I>M. leprae</I> in the induction of MMP-<?xml:namespace prefix = st1 ns = "urn:schemas-microsoft-com:office:smarttags" /><st1:metricconverter ProductID="9 in" w:st="on">9 in</st1:metricconverter> PBMC cultures. These results </SPAN></SPAN><SPAN lang=EN-US style="mso-ansi-language: EN-US; mso-fareast-font-family: Arial">pave the way to new therapeutic interventions to be applied in leprosy patients. Supported by FIOCRUZ, CNPq.</SPAN><SPAN lang=EN-US style="mso-ansi-language: EN-US"><?xml:namespace prefix = o ns = "urn:schemas-microsoft-com:office:office" /><o:p></o:p></SPAN></P></font></p><br><b>Palavras-chave: </b>&nbsp;Leprosy, MMP9, M. leprae, TNF</td></tr></table></tr></td></table></body></html>