Role of MMP9 on Invadopodia Formation in Cells From Adenoid Cystic Carcinoma. Study by Laser Scanning Confocal Microscopy


Autoria(s): NASCIMENTO, Camila F.; GAMA-DE-SOUZA, Leticia N.; FREITAS, Vanessa M.; JAEGER, Ruy G.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2010

Resumo

Migration, invasion and protease activity are essential for tumor progression and metastasis. Metastatic cells rely on invadopodia to degrade and invade extracellular matrix (ECM). Invadopodia are membrane protrusions with enzymes required for ECM degradation. These protrusions contain cortactin and membrane type I matrix metalloproteinase (MT1-MMP) superimposed to areas of digested matrix. Here we characterized invadopodia in a cell line (CAC2) derived from human adenoid cystic carcinoma. We carried out fluorescent-substrate degradation assay to assess in situ protease activity of CAC2 cells. Digestion spots in fluorescent substrate appear as black areas in green background. Cells were cultured on Matrigel-gelatin-FITC and fixed after 1 h and 3 h. CAC2 cells were double labeled to actin and cortactin. Cells were also double stained to actin and MT1-MMR Samples were studied by laser scanning confocal microscopy. In all time points CAC2 cells showed actin, cortactin, and MT1-MMP colocalized with digestion spots in fluorescent substrate. We searched for other proteases involved in invadopodia activity. We have previously demonstrated that MMP9 influences adenoid cystic carcinoma behavior. This prompted us to investigate role played by MMP9 on invadopodia formation. CAC2 cells had MMP9 silenced by siRNA. After I h in fluorescent substrate, cells with silenced MMP9 showed clear decrease in matrix digestion compared with controls. No differences were found in cells with silenced MMP9 grown for 3 h on fluorescent substrate. Our results showed that CAC2 cells exhibit functional invadopodia containing cortactin and MT1-MMR Furthermore, MMP9 would be required in the initial steps of invadopodia formation. Microsc. Res. Tech. 73:99-108, 2010. (C) 2009 Wiley-Liss, Inc.

State of Sao Paulo Research Foundation (FAPESP)[2006/57079-4]

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

State of Sao Paulo Research Foundation (FAPESP)[2008/571.03-8]

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

State of Sao Paulo Research Foundation (FAPESP)[2007/05447-2]

State of Sao Paulo Research Foundation (FAPESP)[2008/55848-6]

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

State of Sao Paulo Research Foundation (FAPESP)[2006/54963-0]

Brazilian Research Council (CNPq)[304868/2006-0]

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Brazilian Research Council (CNPq)[470622/2007-5]

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

FNPESP

FNPESP[2005/55602-9]

Identificador

MICROSCOPY RESEARCH AND TECHNIQUE, v.73, n.2, p.99-108, 2010

1059-910X

http://producao.usp.br/handle/BDPI/28698

10.1002/jemt.20761

http://dx.doi.org/10.1002/jemt.20761

Idioma(s)

eng

Publicador

WILEY-LISS

Relação

Microscopy Research and Technique

Direitos

restrictedAccess

Copyright WILEY-LISS

Palavras-Chave #salivary gland neoplasms #adenoid cystic carcinoma #extracellular matrix #invadopodia #matrix metalloproteinases #cortactin #EXTRACELLULAR-MATRIX DEGRADATION #SALIVARY-GLAND TUMORS #PROTEASE ACTIVITY #CANCER-CELLS #CORTACTIN #INVASION #PEPTIDE #PODOSOMES #LAMININ #SIKVAV #Anatomy & Morphology #Biology #Microscopy
Tipo

article

original article

publishedVersion