章节大纲

    • We have developed a technology to coat cell culture dishes with the collagen fibrils of sturgeons swim bladders.


      Scanning electron micrographs of a culture dish coated with (B) collagen molecules(C) thin fibrilsand (D) thick fibrils


      E, H, and K are polarized light micrographs of mouse osteoblast progenitor cells cultured in each dish. Each shows a characteristic cell morphology, and the cells, especially in K, extend in one direction along the traveling direction of the fibrils (arrow in K). Although not shown in the figure, cell proliferation and differentiation also differ greatly depending on the type of coating. Such coating is not possible with porcine collagen. This technology has made it possible to develop inventive research, such as investigating the reaction of cells to collagen in detail.




      We will further develop this technology, aiming to synthesize three-dimensional cell scaffold materials in the future.