We have described culture methods for normal salivary gland cells, using 3 T 3 cells as a feeder layer. These cultured salivary gland cells are morphologically and biologically similar to normal salivary gland cells. However, the properties of cells cultured
in vivo are unknown. In this paper, the second passage of cultured salivary gland cells was applied to atelocollagen sponges, which were then transplanted to the back of nude mice.
The mice with transplanted cells showed liquid accumulation on the back, whereas the control animals did not.
The liquid was viscous, faint brown in color, and contained amylase (mean, 2175 IU/
l).
Immunohistochemical staining showed that approximately 50 percent of transplanted cells were amylase positive 24 to 48 hours after transplantation. Four weeks after transplantation, the atelo collagen sponge was completely absorbed, and epithelial cells were distributed in a band-like fashion. The transplanted cells did not show ductal or acinar formation. Our results show that salivary gland cells cultured by our method retain the characteristics of salivary gland cells
in vivo.
It may be necessary to establish a novel
in vivo model of salivary glands by using key growth factors.
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