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1.
Two formerly-uncharacterized subunits of 9 kDa and 14 kDa were found in spinach PSI complex. The 9 kDa subunit was released upon removal of antenna chlorophyll complex, whereas the 14 kDa subunit was tightly bound to the core complex. We determined the N-terminal amino acid sequence of the 9 kDa, and an internal sequence of the 14 kDa subunit after protease treatment, since the N-terminus of the latter protein was blocked. These partial sequences suggested that both subunits are new PSI components. 相似文献
2.
Tsuyoshi Uchiyama Shoichi Tomono Koichi Sato Tetsuya Nakamura Masahiko Kurabayashi Fumikazu Okajima 《PloS one》2015,10(10)
Metabolic syndrome is characterized by visceral adiposity, insulin resistance, high triglyceride (TG)- and low high-density lipoprotein cholesterol-levels, hypertension, and diabetes—all of which often cause cardiovascular and cerebrovascular diseases. It remains unclear, however, why visceral adiposity but not subcutaneous adiposity causes insulin resistance and other pathological situations. Lipoprotein lipase (LPL) catalyzes hydrolysis of TG in plasma lipoproteins. In the present study, we investigated whether the effects of angiotensin II (AngII) on TG metabolism are mediated through an effect on LPL expression. Adipose tissues were divided into visceral adipose tissue (VAT) and subcutaneous adipose tissue (SAT) for comparison. AngII accelerated LPL expression in SAT but, on the contrary, suppressed its expression in VAT. In both SAT and VAT, AngII signaled through the same type 1 receptor. In SAT, AngII increased LPL expression via c-Src and p38 MAPK signaling. In VAT, however, AngII reduced LPL expression via the Gq class of G proteins and the subsequent phospholipase C β4 (PLCβ4), protein kinase C β1, nuclear factor κB, and inducible nitric oxide synthase signaling pathways. PLCβ4 small interfering RNA experiments showed that PLCβ4 expression is important for the AngII-induced LPL reduction in VAT, in which PLCβ4 expression increases in the evening and falls at night. Interestingly, PLCβ4 expression in VAT decreased with fasting, while AngII did not decrease LPL expression in VAT in a fasting state. In conclusion, AngII reduces LPL expression through PLCβ4, the expression of which is regulated by feeding in VAT, whereas AngII increases LPL expression in SAT. The different effects of AngII on LPL expression and, hence, TG metabolism in VAT and SAT may partly explain their different contributions to the development of metabolic syndrome. 相似文献
3.
Hikaru Tsukazaki Shigenori Yaguchi Shusei Sato Hideki Hirakawa Yuichi Katayose Hiroyuki Kanamori Kanako Kurita Takeshi Itoh Masahiko Kumagai Satoshi Mizuno Masao Hamada Hiroyuki Fukuoka Ken-ichiro Yamashita John A. McCallum Masayoshi Shigyo Tadayuki Wako 《Molecular breeding : new strategies in plant improvement》2015,35(1):1-11
4.
Akira Makino Anna Miyazaki Ayaka Tomoike Hiroyuki Kimura Kenji Arimitsu Masahiko Hirata Yoshiro Ohmomo Ryuichi Nishii Hidehiko Okazawa Yasushi Kiyono Masahiro Ono Hideo Saji 《Bioorganic & medicinal chemistry》2018,26(8):1609-1613
Tyrosine kinase inhibitors for epidermal growth factor receptor (EGFR-TKIs) are used as molecular targeted therapy for non-small cell lung cancer (NSCLC) patients. The therapy is applied to the patients having EGFR-primary L858R mutation, but drug tolerance caused by EGFR-secondary mutation is occurred within one and half years. For the non-invasive detection of the EGFR-TKIs treatment positive patients by positron emission tomograpy (PET) imagaing, fluorine-18 labeled thienopyrimidine derivative, [18F]FTP2 was newly synthesized. EGFR inhibition assay, cell uptake study, and blocking study indicated [18F]FTP2 binds with high and selective affinity for EGFR with L858R mutation, and not with L858R/T790M dual mutations. On animal PET study using tumor bearing mice, H3255 cells expressing L858R mutated EGFR was more clearly visualized than H1975 cells expressing L858R/T790M dual mutated EGFR. [18F]FTP2 has potential for detecting NSCLC which is susceptible to EGFR-TKI treatment. 相似文献
5.
Shunsuke Takahashi Tomohiro Usui Shohei Kawasaki Hidefumi Miyata Hirofumi Kurita Shun-ichi Matsuura Akira Mizuno Masahiko Oshige Shinji Katsura 《Analytical biochemistry》2014
T7 Exonuclease (T7 Exo) DNA digestion reactions were studied using direct single-molecule observations in microflow channels. DNA digestion reactions were directly observed by staining template DNA double-stranded regions with SYTOX Orange and staining single-stranded (digested) regions with a fluorescently labeled ssDNA-recognizing peptide (ssBP-488). Sequentially acquired photographs demonstrated that a double-stranded region monotonously shortened as a single-stranded region monotonously increased from the free end during a DNA digestion reaction. Furthermore, DNA digestion reactions were directly observed both under pulse-chase conditions and under continuous buffer flow conditions with T7 Exo. Under pulse-chase conditions, the double-stranded regions of λDNA monotonously shortened by a DNA digestion reaction with a single T7 Exo molecule, with an estimated average DNA digestion rate of 5.7 bases/s and a processivity of 6692 bases. Under continuous buffer flow conditions with T7 Exo, some pauses were observed during a DNA digestion reaction and double-stranded regions shortened linearly except during these pauses. The average DNA digestion rate was estimated to be 5.3 bases/s with a processivity of 5072 bases. Thus, the use of our direct single-molecule observations using a fluorescently labeled ssDNA-recognizing peptide (ssBP-488) was an effective analytic method for investigating DNA metabolic processes. 相似文献
6.
Natsumushi is a free image analysis software that offers easy handling and quick measurement, designed especially for entomologists as the main users. The software enables measurement of: (i) color features of a specific region; (ii) area size; (iii) length of simple lines or polylines; and (iv) number of points or their x–y coordinates. Users can specify the region for measurement either manually or automatically by using image thresholding operations. The software is freely available at the website https://staff.aist.go.jp/t-fukatsu/Natsumushi.html . 相似文献
7.
8.
Masahiko Hirata Nobumi Hasegawa Maki Nomura Haruko Ito Kangoro Nogami Tatsunobu Sonoda 《Ecological Research》2009,24(1):119-125
This study monitored deposition and decomposition of cattle dung in a grazed young Chamaecyparis obtusa (an evergreen conifer) plantation in southwestern Japan, as a part of exploring the impacts of livestock in the forest grazing
system. Animals defecated 10–19 times hd−1 day−1, producing feces of 2.2–3.5 kg DM and 33–73 g N per animal per day. The DM and N concentrations of feces ranged from 157–207 g DM kg−1 and 14.8−23.1 g (kg DM)−1, respectively. Occurrence of defecation was spatially heterogeneous, with feces being concentrated mainly on areas for resting
(forest roads, ridges and valleys) and moving (forest roads and along fence lines). Decomposition of dung pats was considerably
slow, showing the rates of 1.37–3.05 mg DM (g DM)−1 day−1 as DM loss. Decomposition was further slower on the basis of N release, 0.51–1.63 mg N (g N)−1 day−1, resulting in steadily increased N concentrations of dung pats with time after deposition. The results show that introduction
of livestock into a forest (i.e., forest grazing) may limit nutrient availability to plants, by redistributing nutrients into
areas with no vegetation (bare land and streams) and by establishing a large N pool as feces due to an imbalance between deposition
and slow release, though further studies are necessary for investigating the occurrence of slow dung decomposition in other
forest situations. 相似文献
9.
Based on its proven anabolic effects on bone in osteoporosis patients, recombinant parathyroid hormone (PTH1-34) has been evaluated as a potential therapy for skeletal repair. In animals, the effect of PTH1-34 has been investigated in various skeletal repair models such as fractures, allografting, spinal arthrodesis and distraction
osteogenesis. These studies have demonstrated that intermittent PTH1-34 treatment enhances and accelerates the skeletal repair process via a number of mechanisms, which include effects on mesenchymal
stem cells, angiogenesis, chondrogenesis, bone formation and resorption. Furthermore, PTH1-34 has been shown to enhance bone repair in challenged animal models of aging, inflammatory arthritis and glucocorticoid-induced
bone loss. This pre-clinical success has led to off-label clinical use and a number of case reports documenting PTH1-34 treatment of delayed-unions and non-unions have been published. Although a recently completed phase 2 clinical trial of PTH1-34 treatment of patients with radius fracture has failed to achieve its primary outcome, largely because of effective healing
in the placebo group, several secondary outcomes are statistically significant, highlighting important issues concerning the
appropriate patient population for PTH1-34 therapy in skeletal repair. Here, we review our current knowledge of the effects of PTH1-34 therapy for bone healing, enumerate several critical unresolved issues (e.g., appropriate dosing regimen and indications)
and discuss the long-term potential of this drug as an adjuvant for endogenous tissue engineering. 相似文献
10.
Nakayama H Miyazaki T Kitamura K Hashimoto K Yanagawa Y Obata K Sakimura K Watanabe M Kano M 《Neuron》2012,74(2):384-396
Functional neural circuit formation during development involves massive elimination of redundant synapses. In the cerebellum, one-to-one connection from excitatory climbing fiber (CF) to Purkinje cell (PC) is established by elimination of early-formed surplus CFs. This process depends on glutamatergic excitatory inputs, but contribution of GABAergic transmission remains unclear. Here, we demonstrate impaired CF synapse elimination in mouse models with diminished GABAergic transmission by mutation of a single allele for the GABA synthesizing enzyme GAD67, by conditional deletion of GAD67 from PCs and GABAergic interneurons or by pharmacological inhibition of cerebellar GAD activity. The impaired CF synapse elimination was rescued by enhancing GABA(A) receptor sensitivity in the cerebellum by locally applied diazepam. Our electrophysiological and Ca2+ imaging data suggest that GABA(A) receptor-mediated inhibition onto the PC soma from molecular layer interneurons influences CF-induced Ca2+ transients in the soma and regulates CF synapse elimination from postnatal day 10 (P10) to around P16. 相似文献