Although progress has been made with respect to the growth and transcription factors implicated in pancreatic development, many questions remain unsolved. It has been established that during embryonic life, both endocrine and acinar cells are derived from pancreatic epithelial precursor cells. Growth factors control the proliferation of precursor cells and their ability to differentiate into mature cells, both in pre-natal and in early post-natal life. Pancreatic development during the early post-natal period is an area of great interest for many scientists. In this study we have examined the structure characteristics, functional and proliferative activity of control and diabetic hamster pancreatic ductal, exocrine and beta cells, following treatment with FGFs 1, 2 and 7 in vitro. Light and electron microscopic studies indicated active synthetic processes in these cells under the influence of the investigated FGFs. In our experimental model of diabetes, the labelling index of the cells was significantly higher than in corresponding control groups of hamsters. We established that FGF2 at a concentration of 10 ng/l was responsible for the most prominent effect on ductal cells and beta cells in the diabetic groups. FGF1 at a concentration of 10 ng/l displayed the highest stimulatory effect on exocrine cells in the diabetic groups at post-natal day 10. Taken together these data strongly suggest that FGF1 and FGF2 induce proliferation of pancreatic epithelial cells during the early post-natal period whereas FGF7 is not strictly specific for pancreatic cell proliferation.

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Copper interferes with numerous physiological processes and can be toxic at low concentrations. We examined the effect of a 2‐week exposure to various concentrations of copper on the structure of the nucleus in maize root meristem cells by transmission electron microscopy. Copper uptake and distribution in the plants, as well as DNA synthesis were also investigated. Treatment with Cu induced alterations in the structure of the nucleus, resulting mainly in a greater density of chromatin. Morphometric analysis showed that the part of the condensed chromatin in the nucleus might be increased by Cu, an observation that was correlated with decreased DNA synthesis as measured by incorporation of 3H‐thymidine. Copper may therefore play a role in chromatin structure and one of the manifestations of Cu toxicity is an alteration in the structure of the nucleus, leading to decreased DNA synthesis.

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