Freeman John A, Chronister Robert B
Department of Biology (JAF), University of South Alabama, 36688, Mobile, AL, USA.
Department of Anatomy and Cell Biology (RBC), University of South Alabama, 36688, Mobile, AL, USA.
Rouxs Arch Dev Biol. 1988 Jan;197(8):490-495. doi: 10.1007/BF00385682.
Cells in developing Artemia franciscana SFB demonstrated tissue-specific differences in DNA content, as determined by fluorescence intensity of bisbenzimide-stained nuclei and by nuclear area. The general epidermis comprised proliferating diploid (2C) cells. The setal cells had 4C-8C DNA content and did not divide during the first two instars. Salt gland cells were polyploid (>8C) and also did not undergo mitosis. Neural cells in the brain were diploid and were replicating. Cells in the thorax region of the gut had a 4C-8C DNA content and were proliferating. The muscle cells in the cephalic appendages contained 2C non-replicating nuclei. Only diploid epidermal cells were involved in segment morphogenesis. There was no difference in number of chromosomes (n=42) in the epidermal cells and the gut cells, indicating that the tissue-specific endopolyploidy was due to endoreduplication.