Involvement of p38α in Kainate-Induced Seizure and Neuronal Cell Damage

We investigated how p38α mitogen-activated protein kinase (p38) is related to kainate-induced epilepsy and neuronal damages, by using the mice with a single copy disruption of the p38 α gene (p38α^+/?). Mortality rate and seizure score of p38α^+/? mice administered with kainate were significantly reduced compared with the case of wild-type (WT) mice. This was clearly supported by the electroencephalography data in which kainate-induced seizure duration and frequency in the brain of p38α^+/? mice were significantly suppressed compared to those of WT mice. As a consequence of seizure, kainate induced delayed neuronal damages in parallel with astrocytic growth in the hippocampus and ectopic innervation of the mossy fibers into the stratum oriens in the CA3 region of hippocampus in WT mice, whose changes were moderate in p38α^+/? mice. Likewise, kainate-induced phosphorylation of calcium/calmodulin-dependent kinase II in the hippocampus of p38α ^+/? mice was significantly decreased compared to that of WT mice. These results suggest that p38α signaling pathway plays an important role in epileptic seizure and excitotoxicity.     

Ontogeny of euthecal and metaseptal structures in colonial scleractinian corals

The ontogenetic development of two Recent scleractinian corals, Golaxea fascicularis (Linnaeus) and Acrhelia horrescens (Dana), has been studied in serial thin sections. The origin of the septotheca (a collective term including both eutheca and pseudotheca) is reconsidered. The eutheca is found to be a basic skeletal structure of corals and of primary origin, formed directly from the basal plate, not by the thickening of septa. The eutheca prepares the way for the formation of metasepta. The ontogenetic growth of the metasepta is illustrated. The pseudotheca is formed by fusion of neighbouring septa and is entirely of secondary origin. Its development is occasional. The essential mural structure of oculinid corals with pseudothecal walls is euthecal.     

Crystalline Ferredoxin from a Blue-Green Alga, Nostoc sp.

Ferredoxin isolated from a blue-green alga, Nostoc sp., was purified and crystallized. The absorption spectrum of Nostoc ferredoxin had, in the oxidized state, peaks at 276, 331, 423, and 470 nm, a pattern characteristic of chloroplast-type ferredoxin. The 423:276 absorption ratio was 0.57. The midpoint oxidation-reduction potential of Nostoc ferredoxin was found to be –406 mV, at pH 7.5. Nostoc ferredoxin mediated the photoreduction of NADP by isolated Nostoc chromato-phores and spinach chloroplasts from which the native ferredoxin was removed. The molar ratio of Nostoc ferredoxin to chlorophyll a was about 1:50, a ratio higher than usually found in photosynthetic cells. The possible evolutionary significance of the properties of Nostoc ferredoxin compared with those of ferredoxins from other photosynthetic organisms is discussed.     

Electron Microscopic Analysis of Phagocytic Activity of Chick Embryonic Retinal pigment cells in vitro

The phagocytosis of latex particles by retinal pigmented cells from chick embryos was studied in vitro. The pigment epithelial cells phagocytized latex particles within 2 hr without a latent period, as found in some mamalian species. The number of latex phagosomes increased with time, and the phagosomes eventually became distributed nearly uniformly in the cytoplasm. When cultures that had been exposed to latex particles for 24 hr were incubated without the particles for a further 7 days, numerous latex phagosomes remained inside the cells without any decrease in their number. This indicates that phagocytized particles are not ejected from the cells, presumably due to a defect in, or absence of, exocytotic activity.     

IMMUNOHISTOCHEMICAL DETECTION OF VITELLOGENIN IN THE OVARY AND FAT BODY DURING A REPRODUCTIVE CYCLE OF THE COCKROACH, BLATTELLA GERMANICA

Vitellogenin was immunohistochemically demonstrated in the ovary and fat body during a reproductive cycle. In terminal oocytes of 4-day adults, vitellogenin began to appear in yolk spherules at the cell periphery. The vitellogenin-containing spherules increased in size and number to occupy the whole cell 2 days later. In the female fat body, vitellogenin began to appear in 3-day adults. It was distributed diffusely in the cytoplasm, at a much lower concentration than in the oocytes, during the vitellogenic period. In 11-day adults whose vitellogenesis had terminated, a higher concentration of vitellogenin was found in the cytoplasmic inclusions of the fat body. Vitellogenin was not detected in the male fat body.     

Effects of photoperiod and temperature on the rhythm and free‐running of adult eclosion in the Indian meal moth Plodia interpunctella

The rhythm of adult eclosion in the Indian meal moth Plodia interpunctella Hübner (Lepidoptera: Pyralidae) is investigated under various photoperiods and temperatures aiming to determine the nature of the temperature compensation and the free‐running period. Insects that are committed to a nondiapause larval development show diel rhythms of adult eclosion at 30, 25 and 20 °C. At 30 °C, the eclosion peak (i.e. the mean time of eclosion) occurs approximately 20 h after lights off under an LD 4 : 20 h photocycle, and at approximately 15 h under an LD 20 : 4 h photocycle. At 25 °C, the peak of eclosion occurs approximately 19 h after lights off under an LD 2 : 20 h photocycle and at approximately 16 h under an LD 20 : 4 h photocycle. At 20 °C, the eclosion peak is significantly advanced under long days of >12 h (i.e. approximately 20 h after lights off under an LD 4 : 20 h photocycle and approximately 9 h under an LD 20 : 4 h photocycle), indicating an effect of both lights‐off and lights‐on signals on the timing of the adult eclosion. To determine the involvement of a self‐sustained oscillator, the rhythm of adult eclosion is examined under darkness at different temperatures (30 to 21 °C). The mean free‐running periods are 22.4, 22.8, 22.0 and 22.5 h at 30, 24, 23 and 22 °C, respectively, indicating that the eclosion rhythm is temperature‐compensated. However, this rhythm does not free‐run under constant darkness at 21 °C. Because a clear diel rhythm is observed under 24‐h photocycles at 20 °C, the oscillator might be damped out within 24 h at the lower temperature.     

Pollination Biology of Hosta sieboldiana (Lodd.) Engler and H. sieboldii (Paxton) J. Ingram (Liliaceae)

Abstract The pollination biology of Hosta sieboldiana and H. sieboldii is investigated comparatively in Central Japan. Both species have homogamous, one-day flowers pollinated by bumblebees. The abdomens of the bees touch the stigma on the extended style when they land on the anthers inside the herkogamous flower, and autogamy is effectively prevented. However, the flowers are fairly self-compatible, and geitonogamy may occur rather frequently because two or more flowers on a scape very often bloom at the same time and many ramets are contiguous. The pollen/ovule ratios suggest that these species are facultative outbreeders. The flower of H. sieboldii seems completely suited to bumblebee pollination. In H. sieboldiana the stigma of the flower, whose style strongly protrudes, is not always touched by bumblebees, but frequent visitation of bumblebees results in pollination of almost all the flowers. Both species have similar pollination systems but seem reproductively isolated by blooming times and habitats. Their common pollinators, however, may sometimes cause introgressive hybridization in contiguous populations.     

PURIFICATION AND PROPERTIES OF THE PROTHORACICOTROPIC HORMONE OF THE SILKWORM, BOMBYX MORI

A simple and highly reproducible procedure for partial purification of prothoracicotropic hormone (PTTH) was established starting with 96,000 male adult Bombyx heads. Approximately 28,500-fold purification of PTTH was accomplished with a yield of about 50% and 6 ng of the most purified preparation ("highly purified PTTH") caused adult development in a brainless Samia pupa. The peptidal nature of PTTH was reconfirmed through the effects of various enzymatic and chemical treatments on the biological activity of "highly purified PTTH". Gel-filtration indicated the molecular weight of PTTH to be 4,400.