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Background The mechanism of body growth in mammals is poorly understood. Here, we investigated the regulatory networks involved in body growth through transcriptomic analysis of pituitary and epiphyseal tissues of smaller sized Debao ponies and Mongolian horses at the juvenile and adult stages. Results We found that growth hormone receptor (GHR) was expressed at low levels in long bones, although growth hormone (GH) was highly expressed in Debao ponies compared with Mongolian horses. Moreover, significant downregulated of the GHR pathway components m-RAS and ATF3 was found in juvenile ponies, which slowed the proliferation of bone osteocytes. However, WNT2 and PLCβ2 were obviously upregulated in juvenile Debao ponies, which led to premature mineralization of the bone extracellular matrix. Furthermore, we found that the WNT/Ca2+ pathway may be responsible for regulating body growth. GHR was demonstrated by q-PCR and Western blot analyses to be expressed at low levels in long bones of Debao ponies. Treatment with WNT antagonistI decreased the expression of WNT pathway components (P GHR pathway components (P IGF-1 gene in the liver was lower in Debao ponies than in Mongolian horses at the juvenile and adult stages. Detection of plasma hormone concentrations showed that Debao ponies expressed higher levels of IGF-1 as juveniles and higher levels of GH as adults than Mongolian horses, indicating that the hormone regulation in Debao ponies differs from that in Mongolian horses. Conclusion Our work provides insights into the genetic regulation of short stature growth in mammals and can provide useful information for the development of therapeutic strategies for small size.

Background. TOSO, also named Fas inhibitory molecule 3 (FAIM3), has recently been identified as an immunoglobulin M (IgM) Fc receptor (FcμR). Previous studies have shown that TOSO is specifically over-expressed in chronic lymphocytic leukemia (CLL). However, the functions of TOSO in CLL remain unknown. The B-cell receptor (BCR) signaling pathway has been reported to be constitutively activated in CLL. Here, we aimed to investigate the functions of TOSO in the BCR signaling pathway and the pathogenesis of CLL. Methods. We over-expressed TOSO in B-cell lymphoma cell lines (Granta-519 and Z138) by lentiviral transduction and knocked down TOSO by siRNA in primary CLL cells. The over-expression and knockdown of TOSO were confirmed at the RNA level by polymerase chain reaction and protein level by Western blotting. Co-immunoprecipitation with TOSO antibody followed by liquid chromatography coupled with tandem mass spectrometry (IP/LCMS) was used to identify TOSO interacting proteins. Western blotting was performed to detect the activation status of BCR signaling pathways as well as B-cell lymphoma 2 (BCL-2). Flow cytometry was used to examine the apoptosis of TOSO-over-expressing B lymphoma cell lines and TOSO-down-regulated CLL cells via the staining of Annexin V and 7-AAD. One-way analyses of variance were used for intergroup comparisons, while independent samples t tests were used for two-sample comparisons. Results. From IP/LCMS, we identified spleen tyrosine kinase (SYK) as a crucial candidate of TOSO-interacting protein and confirmed it by co-immunoprecipitation. After stimulation with anti-IgM, TOSO over-expression increased the phosphorylation of SYK, and subsequently activated the BCR signaling pathway, which could be reversed by a SYK inhibitor. TOSO knockdown in primary CLL cells resulted in reduced SYK phosphorylation as well as attenuated BCR signaling pathway. The apoptosis rates of the Granta-519 and Z138 cells expressing TOSO were (8.46 ± 2.90)% and (4.20 ± 1.21)%, respectively, significantly lower than the rates of the control groups, which were (25.20 ± 4.60)% and (19.72 ± 1.10)%, respectively (P

This report described sample preparation methods that scanning and transmission electron microscope observations, demonstrated by preparing appendages of the woodboring beetle, Chlorophorus caragana Xie & Wang (2012), for both types of electron microscopy. The scanning electron microscopy (SEM) sample preparation protocol was based on sample chemical fixation, dehydration in a series of ethanol baths, drying, and sputter-coating. By adding Tween 20 (Polyoxyethylene sorbitan laurate) to the fixative and the wash solution, the insect body surface of woodboring beetle was washed more cleanly in SEM. This study's transmission electron microscopy (TEM) sample preparation involved a series of steps including fixation, ethanol dehydration, embedding in resin, positioning using fluorescence microscopy, sectioning, and staining. Fixative with Tween 20 enabled penetrate the insect body wall of woodboring beetle more easily than it would had been without Tween 20, and subsequently better fixed tissues and organs in the body, thus yielded clear transmission electron microscope observations of insect sensilla ultrastructures. The next step of this preparation was determining the positions of insect sensilla in the sample embedded in the resin block by using fluorescence microscopy to increase the precision of target sensilla positioning. This improved slicing accuracy.

Three new chlorophenolic glucosides, Curculigine M (1), Curculigine N (2) and Curculigine O (3) were isolated from the dried rhizomes of Curculigo orchioides Gaertn. Their structures were identified by means of spectroscopic methods such as 1D, 2D NMR and MS. These chlorophenolic glycosides were evaluated for effect on osteoblast proliferation against MC3T3-E1 cell line by using MTT assays. Compounds 1, 2 and 3 showed moderate effect on osteoblast proliferation with the proliferation rate of 11.2–15.9%.

Studies showed that the intravascular pH of neutrophils fell to 4.5–5.0 with stimulation for a few minutes. Under this condition, myeloperoxidase was activated to catalyze H2O2 and Cl− to form hypochlorous acid (HOCl). Therefore, it is of significance to develop fluorescence probes for sensing HOCl in acid conditions. In this work, we reported a ratiometric probe CRSH based on a fluorescence resonance energy transfer (FRET) platform for detecting HOCl under acid conditions. Probe CRSH exhibited excellent sensitivity, high selectivity and a rapid response toward HOCl and is suitable for imaging endogenous HOCl in living cells.

Three new labdane-type diterpenoids, callicapene M3-M5 (1–3) were isolated from the Callicarpa macrophylla Vahl. Their structures were identified by spectroscopic method. The isolated compounds were evaluated for inhibitory activity on NO production in LPS-activated RAW 264.7 macrophage cells by using MTT assays. Compounds 1–3 showed potent inhibitory activity, with IC50 value of 48.15, 46.31 and 38.72 μM respectively.

Eucommia ulmoides is a small tree that has evolved strong pest resistance. This study investigated the mechanism of this resistance by evaluating pest damage and antifeedant activity of the seconda...

Chlorophorus caragana (Coleoptera: Cerambycidae) is a trunk borer that feeds on Caragana shrubs in the desert. There are five species of Caragana plant in the distribution area of Ch. caragana. We investigated damaged Caragana plants in the field. Olfactory responses of female Ch. caragana to plants and identified volatile compounds from Caragana plants were further evaluated. Caragana davazamcii was severely damaged in the field, followed by Caragana microphylla. No damage was found to the other three species. Behavioral experiments showed that C. davazamcii, C. microphylla, and Caragana korshinskii were attractive to female insects. Caragana ordosica could repel and avoid female insects. Caragana brachypoda had no effect on the orientation behavior of female insects. Seventy volatile components were identified from the Caragana plants, and (Z)-β-ocimene, 1,3-pentadiene, (Z)-3-hexenyl acetate, perillene, chrysanthenone, and limonene were the most abundant volatiles identified from the Caragana plants. Th...

Chlorophorus caragana is a species of long-horned beetle that damages Caragana davazamcii Sancz. (Fabales: Papilionaceae) bushes in desert areas in China. The beetles cause substantial damage to local forestry plantations and the environment. Sensilla on the maxillary and labial palps of coleopterans a allow the insects to recognize their host plants. We used scanning and transmission electron microscopy to study the ultrastructure, distribution, and abundance of various sensilla on the maxillary and labial palps of C. caragana. We found four types of sensilla including ten subtypes: one of Bohm's bristles, three of sensilla chaetica, one of digitiform sensilla, and five of sensilla twig basiconica. The types and distribution of the sensilla on the maxillary and labial palps were highly similar between males and females. Finally, this article discusses the functions of the sensilla of related species in recognizing hosts and the significance of gustation studies in the context of the control of C. caragana.

A novel compound, 2-(1,5-diphenyl-4,5-dihydro-1H-pyrazol-3-yl)phenyl acrylate (probe L), was designed and synthesized as a highly sensitive and selective fluorescent probe for recognizing and detecting glutathione among cysteine, homocysteine and other amino acids. The structures of related compounds were characterized using IR, NMR and HRMS spectroscopy analysis. The probe is a non-fluorescent compound. On being mixed with glutathione in buffered EtOH:PBS=3:7 solution at pH 7.4, the probe exhibited the blue emission of the pyrazoline at 474 nm and a 83-fold enhancement in fluorescence intensity. This probe is very sensitive and displayed a linear fluorescence off-on response to glutathione with fluorometric detection limit of 8.2 × 10(-8)M. The emission of the probe is pH independent in the physiological pH range. Live-cell imaging of HeLa cells confirmed the cell permeability of the probe and its ability to selectively discriminate GSH from Cys and Hcy in cells. The toxicity of the probe was low in cultured HeLa cells.

Sensory neuron membrane proteins (SNMPs), which are located on the dendritic membrane of olfactory neurons, were considered as important components involved in pheromone reception in insects. In Drosophila melanogaster, mutants without SNMP are unable to evoke neuronal activities in the presence of pheromone cis-vaccenyl acetate (cVA). So deeply understanding the SNMPs functions may help to develop pheromone-mediated insect pest management tactics. The present study reports the identification and characterization of CmedSNMP1 and CmedSNMP2, two candidate SNMPs in the rice leaffolder, Cnaphalocrocis medinalis, one of the serious rice insect pests in Asia. The comparison of amino acid sequences shows that CmedSNMP1 and CmedSNMP2 are very similar to the previously reported SNMPs isolated from moths such as Ostrinia nubilalis and O. furnacalis, respectively, but the two CmedSNMPs share low identity with each other. The distribution patterns of two CmedSNMPs in different tissues of adult moths were examined using RT-PCR and quantitative real-time PCR. Although the two genes are expressed not only in antennae but also in nonolfactory tissues such as wings, legs, and body; the relative transcription level shows both CmedSNMP1 and CmedSNMP2 are highly enriched in antennae. The dN/dS ratios of the two CmedSNMPs indicate that the two genes are all subject to purifying selection and evolved to be functional genes. This work presents for the first time a study on the SNMPs of C. medinalis, which may help in providing guidance to future functional research of moth SNMPs.

Ceramidase plays an important role in regulating the metabolism of sphingolipids, such as ceramide, sphingosine (SPH), and sphingosine-1-phosphate (S1P), by controlling the hydrolysis of ceramide. Here we report the cloning and biochemical characterization of a neutral ceramidase from the red flour beetle Tribolium castaneum which is an important storage pest. The Tribolium castaneum neutral ceramidase (Tncer) is a protein of 696 amino acids. It shares a high degree of similarity in protein sequence to neutral ceramidases from various species. Tncer mRNA levels are higher in the adult stage than in pre-adult stages, and they are higher in the reproductive organs than in head, thorax, and midgut. The mature ovary has higher mRNA levels than the immature ovary. Tncer is localized to the plasma membrane. It uses various ceramides (D-erythro-C(6), C(12), C(16), C(18:1), and C(24:1)-ceramide) as substrates and has an abroad pH optimum for its in vitro activity. Tncer has an optimal temperature of 37 °C for its in vitro activity. Its activity is inhibited by Fe(2+). These results suggest that Tncer has distinct biochemical properties from neutral ceramidases from other species.

Chlorophorus caragana Xie & Wang is a destructive wood-boring beetle that damages Caragana spp. bushes and is distributed in desert areas in north-west China. Using scanning electron microscopy and transmission electron microscopy, we observed the morphology and ultrastructure of antennal and posterior abdominal sensilla in C. caragana females, to discuss the putative functions of these sensilla in host location and oviposition behaviors. In total, seven types (24 subtypes) of sensilla were located on the antenna and posterior abdomen. On the antenna, there were Bohm's bristles (BB.); four subtypes of sensilla chaetica (Ch.1-Ch.4) characterized by non-porous surfaces and sensillum-lymph cavities without dendrites; two subtypes of sensilla trichodea (Tr.1 and Tr.2) with a tip pore and dendrites surrounded by dendritic sheaths; dome-shaped sensilla (Dom.) emerging from a deep cavity with one tip pore; four subtypes of sensilla basiconica (Ba.1-Ba.4) and one type of sensilla auricillica (Au.) with a porous cuticular surface and dendrites in the sensillum-lymph cavity; and one type of sensilla styloconica (Sty.) with grooves on the cuticular wall. On the posterior abdomen, there were four subtypes of sensilla chaetica (Ch.5-Ch.8); three subtypes of sensilla trichodea (Tr.3-Tr.5); and three subtypes of sensilla basiconica (Ba.5-Ba.7; Ba.5 had no groove in the cuticular wall, Ba.6 had one tip pore, and Ba.7 was located in a cuticular cavity). The antennal sensilla were believed to be mechanosensitive, chemosensitive, and sensitive to humidity and temperature, and to play roles in mating, host location and oviposition. The abdominal sensilla are believed to be related to oviposition behaviors.