Evolution of metabolic rates of multicellular organisms is hypothesized to reflect the evolution of their cell architecture. This is likely to stem from a tight link between the sizes of cells and nuclei, which are expected to be inversely related to cell metabolism. Here, we analysed basal metabolic rate (BMR), internal organ masses and the cell/nucleus size in different tissues of laboratory mice divergently selected for high/low mass-corrected BMR and four random-bred mouse lines. Random-bred lines had intermediate levels of BMR as compared to low-and high-BMR lines. Yet, this pattern was only partly consistent with the between-line differences in cell/nucleus sizes. Erythrocytes and skin epithelium cells were smaller in the high-BMR line than in other lines, but the cells of low-BMR and random-bred mice were similar in size. On the other hand, the size of hepatocytes, kidney proximal tubule cells and duodenum enterocytes were larger in high-BMR mice than other lines. All cell and nucleus sizes were positively correlated, which supports the role of the nucleus in cell size regulation. Our results suggest that the evolution of high BMR involves a reduction in cell size in specialized tissues, whose functions are primarily dictated by surface-to-volume ratios, such as erythrocytes. High BMR may, however, also incur an increase in cell size in tissues with an intense transcription and translation, such as hepatocytes.

Cell size plays a role in evolutionary and phenotypically plastic changes in body size. To examine this role, we measured the sizes of seven cell types of geckos (Paroedura picta) reared at three constant temperatures (24, 27, and 30°C). Our results show that the cell size varies according to the body size, sex and developmental temperature, but the pattern of this variance depends on the cell type. We identified three groups of cell types, and the cell sizes changed in a coordinated manner within each group. Larger geckos had larger erythrocytes, striated muscle cells and hepatocytes (our first cell group), but their renal proximal tubule cells and duodenal enterocytes (our second cell group), as well as tracheal chondrocytes and epithelial skin cells (our third cell group), were largely unrelated to the body size. For six cell types, we also measured the nuclei and found that larger cells had larger nuclei. The relative sizes of the nuclei were not invariant but varied in a complex manner with temperature and sex. In conclusion, we provide evidence suggesting that changes in cell size might be commonly involved in the origin of thermal and sexual differences in adult size. A recent theory predicts that smaller cells speed up metabolism but demand more energy for their maintenance; consequently, the cell size matches the metabolic demand and supply, which in ectotherms, largely depends on the thermal conditions. The complex thermal dependency of cell size in geckos suggests that further advancements in understanding the adaptive value of cell size requires the consideration of tissue-specific demand/supply conditions.

The objective of this study was to examine a relationship between cadmium (Cd) accumulation and histopathological changes in the kidneys and liver of magpies (Pica pica) from a zinc smelter area. The concentrations of metallothionein (MT) and glutathione (GSH) that are linked to a protective effect against Cd toxicity were also determined. There was a positive correlation between the concentration of Cd (2.2-17.9 microg/g) and histopathological changes (interstitial inflammation and tubular cell degeneration) in the kidneys (R (s) = 0.87, P = 0.0000). The renal Cd also positively correlated with apoptosis (R (s) = 0.72, P = 0.0005) but the metal did not affect lipid peroxidation. Notably, the average concentration of Cd in the kidneys exceeded MT capacity by about 7 microg/g which is thought to produce renal injury. Importantly, GSH level in the kidneys of magpies from the polluted area dropped to 38% of that observed in the reference birds, probably potentiating Cd toxicity. On the contrary, the liver accumulation of Cd was relatively small (0.88-3.38 microg/g), the hepatic MT capacity exceeded the total concentration of Cd and no association between the hepatic Cd and histopathology was found despite the fact that GSH level was only half that observed in the reference birds. The data suggest that Cd intoxication may be responsible for histopathological changes occurring in the kidneys of free-ranging magpies and that the pathology may be associated with inappropriate amount of renal MT and GSH.

The objective of this study was to examine relations between basal metabolic rate (BMR) and cadmium (Cd) accumulation in the liver, kidneys, and duodenum in mice. The 5-month-old mice selected for high (H) and low (L) BMR were exposed for 8 weeks to 0, 10, and 100 μg Cd/mL of drinking water. The H-BMR mice showed significantly higher concentrations of Cd in the liver (47-79%), kidneys (61-70%), and duodenum (74-100%) than L-BMR animals. The tissue Cd accumulation also positively correlated with the duodenal iron which, in turn, was positively associated with BMR (Spearman R (s) = 0.81, P = 0.0004). The data indicate that tissue accumulation of Cd in mice is linked to BMR; the correlation between tissue Cd and duodenal iron suggests an involvement of iron transport pathway in the accumulation of Cd.

Adult male bank voles undergo the body and organ regression before winter, and in early spring, they resume the growth and reproductive processes. The aim of the present study was to determine whether the seasonal changes of body and organ weight in these animals depend on changes in the number of cells or their size. To study an autumnal regression, wild adult males captured in August were exposed to short photoperiod for 0, 4, and 8 weeks, while to study a spring resumption, overwintered males caught in March were exposed to long photoperiod for 0, 1, and 4 weeks. Apoptosis, proliferation, and cell size in the skeletal muscles, liver, and testes were examined. The study revealed that the seasonal changes of testes weight were associated with changes in the number of testicular cells. On the contrary, the changes in size of skeletal myocytes and hepatocytes appeared to be responsible for the seasonal changes of body (muscle) and liver weights in these rodents.