HISTOLOGY AND HISTOPATHOLOGY

From Cell Biology to Tissue Engineering

 

Gastrospheres of human gastric mucosa cells: an in vitro model of stromal and epithelial stem cell niche reconstruction

Carlos A.N. Santos1, Leonardo R. Andrade2, Márcia H.M. Costa3, Heitor S.P. Souza3, José M. Granjeiro1, Christina M. Takiya2, Radovan Borojevic1 and Luiz E. Nasciutti2

1Institute National of Metrology, Quality and Technology - INMETRO, Xerém, 2Institute of Biomedical Sciences, Federal University of Rio de Janeiro, Ilha do Fundão and 3Multidisciplinar Laboratory, Clementino Fraga Filho University Hospital, Federal University of Rio de Janeiro, Ilha do Fundão, Rio de Janeiro, Brazil

Offprint requests to: Luiz Eurico Nasciutti, Laboratório de Interações Celulares, Programa de Pesquisa em Biologia Celular e do Desenvolvimento, Instituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, Cidade Universitária - Ilha do Fundão, 21941-590, Rio de Janeiro, Brazil. e-mail: luiz.nasciutti@histo.ufrj.br or luiz.nasciutti@icb.ufrj.br


Summary. The molecular characterization of mechanisms involved in the gastrointestinal tract disorders needs an in vitro 3D culture model able to mimic the in vivo gastric microenvironment. Herein, we propose a 3D coculture system where gastric epithelial and stromal cells are grown together building spherical and solid structures using the NASA bioreactor - cell culture system (RCCS), a bioreactor. Epithelial and stromal cells from human antral gastric mucosa were isolated from endoscopic gastric biopsies. Thereafter, these cells were mechanically and enzymatically dispersed by treatment with dispase and collagenase, respectively. Using specific culture procedures, these cells formed 3D structures by using a RCCS, named "gastrospheres". Briefly, gastrospheres were obtained by initial seeding of 2.5x104 cells/well in 96 well culture plates. At 24 h after their formation, they were transferred into RCCS, and maintained for 7, 14, 21, and 28 days. The gastrospheres were morphologically characterized by immunocytochemisty to evaluate extracellular matrix (ECM), and by electron microscopy. These analysis of gastrospheres revealed that the epithelial cells were cytokeratin (CK) and lectin reactive and were arranged in the outer layer; stromal cells presented long cytoplasmic processes and were localized inside the gastrosphere. They were vimentin (VIM) and α-smooth muscle actin (α-SMA) positive and expressed ECM components such as laminin (LN), fibronectin (FN), and type IV collagen (CIV). Electron microscopy revealed groups of cohesive gastric cells surrounded by complex stromal structures, with multiple microvilli, and tight cellular junctions interspersed with extracellular matrix fibrils and fibers. The presence of some nestin-positive cells was observed in the inner region of the gastrospheres, suggesting an intermediary localization between epithelial and stromal cells. Altogether, our data suggest that in vitro gastrospheres recapitulate the in vivo gastric niche microenvironment. Histol Histopathol 31, 879-895 (2016)

Key words: Gastrospheres, Human gastric stromal and epithelial cells, Nestin-positive epithelial cells

DOI: 10.14670/HH-11-726