Effect of Recombinant Matrix Metalloproteinase Type II (MMP-2) On Aortas of Adult Mice After Systemic Administration

  • Autor
  • Stefanne de Cássia Pereira da Silva
  • Co-autores
  • Pricila Rodrigues Gonçalves , Wictoria Farias Dias , Thayná Matos da Cunha Catete , David Silva da Costa , Marta Chagas Monteiro , Keuri Eleutério Rodrigues , Raquel Fernanda Gerlach , Alejandro Ferraz do Prado
  • Resumo
  •  

    Introduction: The increase in MMP-2, an extracellular matrix metalloproteinase, is linked to the pathophysiology of several cardiovascular diseases. In the arteries of aging animals, this effect is associated with increased fibrosis by TGF-?1 cytokine. We hypothesize that treatment with recombinant MMP-2 in mice for four weeks promotes morphological changes, such as increased collagen and elastin in the aortas. Objective:  This study aimed to evaluate the morphological changes in mice's aorta after four weeks of treatment with recombinant MMP-2. Methods: MMP-2 was expressed and purified in E. coli bacteria stem from the pET5a_rhMMP-2 clone. Quantification of MMP-2 was performed using a BCA kit assay. The MMP-2 activity and purity assessments were determined by gel zymography and silver staining. C57BL / 6 [Wild type (Wt)] male mice young adults (7 weeks) (CEUA n° 6175230518), with 20-25g, separated into two groups. MMP-2 group was treated with rhMMP-2 (150 ng/g/i.p);), and the control group was treated with control (0.9% saline solution). Elastin and collagen contents were evaluated using hematoxylin/eosin, orcein, and Picro Sirius red-stain sections. Results: Recombinant MMP-2 administration for four weeks did not change the thickness of the aortic medial layer, the elastin, and collagen content compared to the control animals. Conclusion: No morphological changes were observed in this study. Thus, we will carry out biochemical measurements to verify changes in the aortas' oxidative system due to the increase in MMP-2 levels.

  • Palavras-chave
  • Fibrosis; aorta remodeling; hypertrophy
  • Modalidade
  • Vídeos
  • Área Temática
  • Inflamação e doenças vasculares
Voltar
  • Estresse oxidativo
  • Disfunção endotelial
  • Produtos naturais
  • Inflamação e doenças vasculares
  • Sinalização celular
  • Tecido adiposo perivascular
  • Sistema endócrino e doenças vasculares
  • Revisões, projetos, revisões sistemáticas e metanálises em biologia vascular
  • Educação em saúde e doenças vasculares
  • COVID-19 e complicações vasculares

Comissão Organizadora

José Wilson do Nascimento Corrêa
Simone Potje
Gabriel Tavares do Vale
Stêfany Cau
Roger Lyrio
Simone R Potje
Alice Valença Araújo
Ruth Cristina Albuquerque Santos
Lara Caroline Amaro
Ana Dária Cassoli da Silva
Pollyana Peixoto
Izabela Moreira Bonfim
Jocimar José Pitol
Sunamita Vaz Martins
Izabela Moreira Bonfim
Palloma Emanuelle Dornelas de Melo
Daniella Bonaventura
Tagana Rosa
Sarah Victory Santana Gomes
Priscila Cruz
André Lucas Borges
Jéssyca Aparecida Soares Giesen
Leticia Tinoco Gonçalves
Silvia Maria Luna Alves
NAYANA YARED BATISTA
Wellington Francisco Pereira da Silva
Natália Ferreira de Araújo
Leandro de Carvalho Gomes

Comissão Científica