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Naoki Tokuhara Kana Namiki Mai Uesugi Chihiro Miyamoto Makoto Ohgoh Katsutoshi Ido Takashi Yoshinaga Toshihiko Yamauchi Junro Kuromitsu Sadao Kimura Norimasa Miyamoto Yoshitoshi Kasuya 《The Journal of biological chemistry》2010,285(43):33294-33306
One of the family of voltage-gated calcium channels (VGCC), the N-type Ca2+ channel, is located predominantly in neurons and is associated with a variety of neuronal responses, including neurodegeneration. A precise mechanism for how the N-type Ca2+ channel plays a role in neurodegenerative disease, however, is unknown. In this study, we immunized N-type Ca2+ channel α1B-deficient (α1B−/−) mice and their wild type (WT) littermates with myelin oligodendrocyte glycoprotein 35–55 and analyzed the progression of experimental autoimmune encephalomyelitis (EAE). The neurological symptoms of EAE in the α1B−/− mice were less severe than in the WT mice. In conjunction with these results, sections of the spinal cord (SC) from α1B−/− mice revealed a reduction in both leukocytic infiltration and demyelination compared with WT mice. No differences were observed in the delayed-type hypersensitivity response, spleen cell proliferation, or cytokine production from splenocytes between the two genotypes. On the other hand, Western blot array analysis and RT-PCR revealed that a typical increase in the expression of MCP-1 in the SC showed a good correlation with the infiltration of leukocytes into the SC. Likewise, immunohistochemical analysis showed that the predominant source of MCP-1 was activated microglia. The cytokine-induced production of MCP-1 in primary cultured microglia from WT mice was significantly higher than that from α1B−/− mice and was significantly inhibited by a selective N-type Ca2+ channel antagonist, ω-conotoxin GVIA or a withdrawal of extracellular Ca2+. These results suggest that the N-type Ca2+ channel is involved in the pathogenesis of EAE at least in part by regulating MCP-1 production by microglia. 相似文献
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Eiiti Kasuya 《Population Ecology》1993,35(2):251-255
An index of intensity of sexual selection proposed by Nishida (1992: Res. Popul. Ecol. 34: 373–382) was examined. Two examples were presented to show that Nishida's index was not free from confounding effect of mortality schedule. Importance of removing the phylogenetic effects in comparative analyses was also discussed. 相似文献
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Recent studies have documented male traits that cause physical harm to their mates during copulation. However, whether or not males sustain injuries during copulation has not been investigated except in sexually cannibalistic species. We found that males were injured by females during copulation in the polygynous cricket Meloimorpha japonica . More than half of the males sustained injuries to their forewings and/or genitalia during copulation. The probability of injury increased with the duration of copulation. The remating rate of females was high when the copulation duration in the first mating was short. These results suggest that copulation duration will be affected by the compromise between the risk of injury for males and paternity assurance. 相似文献
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Takayoshi Suzuki Yuki Kasuya Yukihiro Itoh Yosuke Ota Peng Zhan Kaori Asamitsu Hidehiko Nakagawa Takashi Okamoto Naoki Miyata 《PloS one》2013,8(7)
To find histone deacetylase 3 (HDAC3)-selective inhibitors, a series of 504 candidates was assembled using “click chemistry”, by reacting nine alkynes bearing a zinc-binding group with 56 azide building blocks in the presence of Cu(I) catalyst. Screening of the 504-member triazole library against HDAC3 and other HDAC isozymes led to the identification of potent and selective HDAC3 inhibitors T247 and T326. These compounds showed potent HDAC3 inhibition with submicromolar IC50s, whereas they did not strongly inhibit other isozymes. Compounds T247 and T326 also induced a dose-dependent selective increase of NF-κB acetylation in human colon cancer HCT116 cells, indicating selective inhibition of HDAC3 in the cells. In addition, these HDAC3-selective inhibitors induced growth inhibition of cancer cells, and activated HIV gene expression in latent HIV-infected cells. These findings indicate that HDAC3-selective inhibitors are promising candidates for anticancer drugs and antiviral agents. This work also suggests the usefulness of the click chemistry approach to find isozyme-selective HDAC inhibitors. 相似文献
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Motoyuki Iemitsu Seiji Maeda Subrina Jesmin Takeshi Otsuki Yoshitoshi Kasuya Takashi Miyauchi 《Journal of applied physiology》2006,101(1):151-163
Since exercise training causes cardiac hypertrophy and a single bout induces mechanical stress to the heart, the present study aimed to characterize the activation patterns of multiple MAPK signaling pathways in the heart after a single bout of exercise or chronic exercises. The hearts of untrained rats received 5, 15, and 30 min of treadmill running exercise (Ex5 to Ex30) and rested for 0.5, 1, 3, 6, 12, and 24 h (PostEx0.5 to PostEx24) before subjecting them to the following different experiments. Activation of MAPKs (ERK, JNK, and p38) and MAPKKs (MEK1/2, SEK, and MKK3/6) increased immediately after acute exercise in a time-dependent manner, with ERK, JNK, and p38 peaking at Ex15, Ex15, and Ex30, respectively. Expression of immediate early genes (c-fos, c-jun, and c-myc) was augmented and activator protein-1 DNA binding activity was enhanced in untrained rats immediately after a single bout of exercise. The elevated levels of MAPKs declined to the resting levels within 24 h after exercise. In another set of experiments, following 4, 8, and 12 wk of exercise training, the rats exhibited significant cardiac hypertrophy by week 12. Activation of MAPKs in the 4-wk-trained rats increased after a 30-min single bout of exercise but decreased in the 8-wk group. Finally, the activity of MAPKs signaling in the 12-wk-trained rats exposed to an acute bout of exercise was unaltered. We conclude that exercise induces the activation of multiple MAPK (ERK, JNK, and p38) pathways in the heart, an effect that gradually declines with the development of exercise-induced cardiac hypertrophy. 相似文献
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Hiroyuki Hirayama Eiiti Kasuya 《Ethology : formerly Zeitschrift fur Tierpsychologie》2014,120(12):1228-1236
Many studies have shown the benefits of selecting suitable sites for offspring survival and growth. However, costs of selecting suitable sites have been little covered. If the female's costs associated with selecting suitable sites exceed the benefit from improvement of offspring performance, selecting such sites can have a negative effect on the ongoing reproductive success for ovipositing females. We investigate the potential costs of selecting suitable sites in the water strider Aquarius paludum insularis. Where there exists a risk of egg parasitism, the female A. paludum will submerge and select a deep site, more suitable for offspring survival, for oviposition. By forcing A. paludum underwater once a day for 10 d, we investigated the potential costs associated with oviposition at deep sites, firstly relating to the performance of submergence (latency to asphyxiation or proportion of buoyancy loss) and, secondly, in the number of eggs laid. Buoyancy became weaker and the latency to asphyxiation became shorter with the number of submergences. The number of eggs laid in the period of forced submergence was smaller than both before and after the period. Selecting deep sites can therefore increase the mortality risk of ovipositing females and also decrease the number of eggs laid in their lives. Selecting suitable sites in all the oviposition bouts can decrease ovipositing females' reproductive success. Costs, not only benefits, should be taken into consideration for understanding oviposition site selection during the lifespan of an ovipositing female. 相似文献