The effects of forest fragmentation on the population ecology and natural history of a funnel-web spider

Habitat fragmentation strongly affects the abundance, distribution, body size and population genetics of invertebrates. Urban growth in Brazil has led to severe fragmentation, especially in the Atlantic Forest and savannas. The effects of this fragmentation on the common funnel-web spider Aglaoctenus lagotis were examined in two forest fragments within the interior savanna: a smaller fragment within an urban environment and a larger fragment within a rural environment. The reproductive period occurred in October, coinciding with the beginning of the rainy season, when the species was aggregated in the two forest fragments. The smaller fragment contained a larger population, and the spiders had a larger average prosoma size and web area. The presence of a larger population in a smaller area within the urban centre may reflect a limited dispersal ability, reduced predator abundance or low interspecific competition. The larger prosoma length and web area in the smaller habitat fragment suggest greater resource availability and a higher probability of capturing prey in the urban environment. In both areas, a larger number of capture threads was positively correlated with the presence of inquiline spiders in the webs. The genetic data indicate close similarity between and within the two areas, indicating that the species has low genetic variability or that the areas studied, consistent with their proximity, have separated only recently. Most savannas and forests in midwestern Brazil have recently undergone severe fragmentation, and further studies of this nature are needed.     

Targeting mitochondria by α-tocopheryl succinate overcomes hypoxia-mediated tumor cell resistance to treatment

Rapidly proliferating tumor cells easily become hypoxic. This results in acquired stability towards treatment with anticancer drugs. Here, we show that cells grown at 0.1 % oxygen are more resistant towards treatment with the conventionally used anticancer drugs doxorubicin and cisplatin. The stimulation of apoptosis, as assessed by the number of cells in the SubG1 fraction of the cell cycle, release of cytochrome c into the cytosol, activation of caspase-3, and cleavage of PARP, was markedly suppressed under low oxygen content or when hypoxia was mimicked by deferoxamine. Hypoxia or deferoxamine treatment was accompanied by stabilization of the hypoxia-inducible factor (HIF-1). The downregulation of HIF-1 using siRNA technique restored cell sensitivity to treatment under hypoxic conditions to the levels detected under normoxic conditions. In contrast to cisplatin or doxorubicin, α-tocopheryl succinate (α-TOS), a compound that targets mitochondria, stimulated cell death irrespective of the oxygen concentration. Moreover, under hypoxic condition cell death induced by α-TOS was even enhanced. Thus, α-TOS can successfully overcome resistance to treatment caused by hypoxia, which makes α-TOS an attractive candidate for antitumor therapy via mitochondrial targeting.     

Regulation of male sex determination: genital ridge formation and Sry activation in mice

Sex determination is essential for the sexual reproduction to generate the next generation by the formation of functional male or female gametes. In mammals, primary sex determination is commenced by the presence or absence of the Y chromosome, which controls the fate of the gonadal primordium. The somatic precursor of gonads, the genital ridge is formed at the mid-gestation stage and gives rise to one of two organs, a testis or an ovary. The fate of the genital ridge, which is governed by the differentiation of somatic cells into Sertoli cells in the testes or granulosa cells in the ovaries, further determines the sex of an individual and their germ cells. Mutation studies in human patients with disorders of sex development and mouse models have revealed factors that are involved in mammalian sex determination. In most of mammals, a single genetic trigger, the Y-linked gene Sry (sex determination region on Y chromosome), regulates testicular differentiation. Despite identification of Sry in 1990, precise mechanisms underlying the sex determination of bipotential genital ridges are still largely unknown. Here, we review the recent progress that has provided new insights into the mechanisms underlying genital ridge formation as well as the regulation of Sry expression and its functions in male sex determination of mice.