The sub-cellular localization of annexin V in cultured chick-embryo fibroblasts.

Effect of Adenosine Agonists on the Proliferation and Differentiation of Chick Embryo Fibroblasts in Three Dimensional Reconstituted Tissue Constructs

Previous studies indicate that organ fibroblasts play an important role in wound healing, collagen production, remodeling processes and pathogenesis of progressive heart, lung, renal and hepatic fibrotic diseases. Several studies suggest a possible inhibitory role for adenosine in the regulation of fibroblast proliferation. The effect of adenosine A2 agonists on proliferation and differentiatio...

Evaluation and Optimization of Chick Embryo Fibroblasts for Production of a Fowl Pox Vaccine Based on Cell Culture

Abstract Background and Aims: For more than half a century, the production of fowl pox vaccine at Razi Vaccine and Serum Research Institute, has been carried out by injection method in the chick chorioallantoic membrane (CAM) and the vaccine has a favorable and effective in poultry flocks and has provided a complete satisfaction to the poultry flocks owner. Fowl pox vaccine is also manufactured...

Fowl Spirochaetosis in Iran with special reference to control the disease by immunization with a formolized chick-embryo vaccine.

Cellular Dynamics after Injection of Mesoderm-Derived Human Embryonic Kidney 293 Cells and Fibroblasts into Developing Chick Embryos

This study was conducted to compare localization of transformed or differentiated cells after injection into developing chick embryos. Mesoderm-derived chicken embryonic fibroblasts (CEFs), retrieved from normal tissues and artificially transformed human embryonic kidney (HEK) 293 cells, were injected into the dorsal aorta of stage 17 embryos, incubated for 60 h, and post-injection survival and...

Plaquing of Toxoplasma gondii in secondary cultures of chick embryo fibroblasts.

A tissue culture system that employed chick embryo fibroblasts was described for plaquing of the obligate intracellular parasite Toxoplasma gondii. High plaquing efficiency and reproducibility were accomplished by the use of secondary rather than primary cultures and the use of toxoplasma obtained from disrupted peritoneal cells of mice infected 48 hr earlier. The monolayers were cultured in a ...