MGT

  • 文章类型: Journal Article
    Mg-K稳态对于植物对非生物胁迫的反应至关重要,但它的规定在很大程度上仍然未知。从苜蓿中克隆的MsWRKY44在叶片和叶柄中高表达。它的过度表达抑制了苜蓿的生长,并促进叶片衰老和苜蓿对酸和铝胁迫的敏感性。叶尖,在pH4.5和pH4.5Al条件下,MsWRKY44-OE植物的边缘和叶间出现黄色斑点。同时,随着MsWRKY44-OE植物枝条中K积累的减少和Mg和Al积累的增加,Mg-K稳态发生了实质性变化。Further,发现MsWRKY44直接结合MsMGT7和MsCIPK23的启动子,并正激活它们的表达。烟草叶片中瞬时过表达的MsMGT7和MsCIPK23增加了Mg和Al的积累,但降低了K的积累。这些结果揭示了一个新的调控模块MsWRKY44-MsMGT7/MsCIPK23,它影响Mg和K在芽中的运输和积累,并促进苜蓿对酸和铝胁迫的敏感性。
    Mg-K homeostasis is essential for plant response to abiotic stress, but its regulation remains largely unknown. MsWRKY44 cloned from alfalfa was highly expressed in leaves and petioles. Overexpression of it inhibited alfalfa growth, and promoted leaf senescence and alfalfa sensitivities to acid and Al stresses. The leaf tips, margins and interveins of old leaves occurred yellow spots in MsWRKY44-OE plants under pH4.5 and pH4.5 +Al conditions. Meanwhile, Mg-K homeostasis was substantially changed with reduction of K accumulation and increases of Mg as well as Al accumulation in shoots of MsWRKY44-OE plants. Further, MsWRKY44 was found to directly bind to the promoters of MsMGT7 and MsCIPK23, and positively activated their expression. Transiently overexpressed MsMGT7 and MsCIPK23 in tobacco leaves increased the Mg and Al accumulations but decreased K accumulation. These results revealed a novel regulatory module MsWRKY44-MsMGT7/MsCIPK23, which affects the transport and accumulation of Mg and K in shoots, and promotes alfalfa sensitivities to acid and Al stresses.
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  • 文章类型: Journal Article
    乳腺肿瘤(MGT)是雌性犬中常见的肿瘤。然而,多年来一直有报道雄性犬中罕见的MGT病例。由于与雌性狗相比,雄性狗的MGT发病率较低,兽医肿瘤学主要集中在母犬中诊断的乳腺肿瘤,并在该科学领域进行了广泛的研究。因此,没有足够的关于雄性犬的流行病学数据,其肿瘤发展的病因仍然知之甚少。这篇文献综述的目的是介绍雄性狗的MGT病例,以更好地了解多年来问题的严重程度。对74只受影响的雄性犬的92例肿瘤的分析表明,雄性犬的大多数MGT是良性肿瘤(54.3%),尤其是腺瘤的形式,常发育于犬乳腺后部(58.1%)。注意到7-13岁的雄性狗中犬MGT的数量增加,年龄峰值在11岁。受影响动物的年龄与品种无关。乳腺肿瘤主要在杂交品种(20.2%)中被诊断出来,其次是可卡犬(18.9%)和德国牧羊犬(10.8%)。多年来一直在讨论雄性狗的MGT发育与睾丸肿瘤(TT)的共同发生之间的关联。因此,本研究包括两种肿瘤发展的病例.因此,仅在12.7%的MGT病例中还描述了TT的病史。因此,不应假定这些肿瘤之间存在一般关联.
    Mammary gland tumours (MGTs) are commonly occurring neoplasms in female dogs. However, rare cases of MGTs in male dogs have been reported for years. Due to the low incidence of MGTs in male dogs in comparison to female dogs, veterinary oncology is mainly focused on mammary neoplasms diagnosed in female dogs and extensive research is conducted in this scientific area. Therefore, there are no sufficient epidemiological data on male dogs and the aetiology of their tumour development is still poorly understood.The aim of this literature review was to present cases of MGTs in male dogs for better understanding the scale of the problem over the years. The analyses of 74 affected male dogs with 92 tumours showed that the majority of MGTs in male dogs were benign tumours (54.3%), especially in form of adenomas, often developed in posterior canine mammary glands (58.1%).The increased number of canine MGTs in male dogs aged 7 -13 years with an age peak at 11 years was noted. The age of affected animals was not related to breed. Mammary gland neoplasms were diagnosed predominately in Crossbreeds (20.2%) followed by Cocker Spaniels (18.9%) and German Shepherds (10.8%).The association between MGT development in male dogs and co-occurrence of testicular tumours (TTs) has been discussed for years. Thus, cases of development of both tumours were included in this study. As a result, only in 12.7% cases of MGTs also history of TTs was described. Therefore, no general association between these tumours should be assumed.
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  • 文章类型: Journal Article
    颗粒细胞瘤(GCT)占所有软组织肉瘤(STS)的0.5%,当转移时,他们表现出攻击性行为并决定有限的生存。转移性GCT相对耐药;然而,越来越多的证据表明,在本组织学研究中使用帕唑帕尼和其他靶向治疗有益处.本文就帕唑帕尼及其他靶向治疗在GCTs治疗中的作用作一综述,以及GCT中描述的病理学和分子生物学的一些见解。在我们的搜索中找到的256篇文章中,10篇病例报告文章符合纳入标准。帕唑帕尼是最常用的全身疗法。帕唑帕尼治疗的中位报告时间为7个月。十分之八的患者(80%)经历了帕唑帕尼的疾病控制,而十分之四(40%)的患者实现了客观的RECIST反应。分子研究表明,帕唑帕尼在GCT中的抗肿瘤作用可能是由于ATP6AP1/2基因的功能丧失,从而通过几种分子途径增强信号传导,如SFKs,STAT5a/b,和PDGFR-β。其他报道的恶性GCTs靶向治疗包括帕唑帕尼联合克唑替尼,显示一名患者的疾病控制了四个月,和PI3K抑制剂,在另一名患者中实现了9个月的疾病控制。达沙替尼和甲地孕酮在另外两个不同的患者中无效。帕唑帕尼已被证明在晚期GCTs中具有活性,可被视为优选的治疗选择。
    Granular cell tumors (GCT) represent 0.5% of all soft tissue sarcomas (STS), and when metastatic, they exhibit aggressive behavior and determine limited survival. Metastatic GCTs are relatively chemo-resistant; however, there is growing evidence of the benefit of using pazopanib and other targeted therapies in this histology. This is a review of the role of pazopanib and other targeted therapies in the treatment of GCTs, along with some insights on pathology and molecular biology described in GCTs. From 256 articles found in our search, 10 case-report articles met the inclusion criteria. Pazopanib was the most employed systemic therapy. The median reported time on therapy with pazopanib was seven months. Eight out of ten patients (80%) experienced disease control with pazopanib, while four out of ten (40%) patients achieved an objective RECIST response. Molecular studies suggested that antitumoral effects of pazopanib in GCT might be due to a loss-of-function of ATP6AP1/2 genes which consequently enhance signaling through several molecular pathways, such as SFKs, STAT5a/b, and PDGFR-β. Other reported targeted therapies for malignant GCTs included pazopanib in combination with crizotinib, which showed disease control for four months in one patient, and a PI3K inhibitor which achieved disease control for nine months in another patient. Dasatinib and megestrol were ineffective in two other different patients. Pazopanib has been demonstrated to be active in advanced GCTs and may be considered as a preferable treatment option.
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  • 文章类型: Journal Article
    肠炎沙门氏菌是人类食源性沙门氏菌感染和暴发的主要原因。有效监测和及时发现疫情对于公共卫生控制至关重要。具有多级分辨率的多级基因组分型(MGT)先前已被证明是用于此目的的有希望的工具。在这项研究中,我们为肠炎S.开发了9个水平的MGT,并详细描述了肠炎S.的基因组流行病学特征.我们检查了来自86个国家101年的分离株的26670个公开可用的肠炎沙门氏菌基因组序列,以揭示其时空分布。使用较低分辨率的MGT级别,确定了全球流行和区域限制的序列类型(STs);发现了在美国人类病例中常见的鸟类相关MGT4-STs;从2014年至2018年,在英国观察到MGT5-STs的时间趋势,揭示了长寿的地方性STs和新STs的快速扩展。使用MGT3到MGT6,我们在各种MGT水平上鉴定了多药耐药(MDR)相关的STs,这提高了MDR克隆的检测和全局跟踪的精度。我们还发现,全球大多数肠炎沙门氏菌种群属于两个主要谱系,导致大规模爆发的倾向明显不同。已建立了在线开放的MGT数据库,以对肠炎S.进行统一的国际监测。我们证明了MGT为肠炎沙门氏菌监测和暴发检测提供了灵活且高分辨率的基因组分型工具。
    Salmonella enterica serovar Enteritidis is a major cause of foodborne Salmonella infections and outbreaks in humans. Effective surveillance and timely outbreak detection are essential for public health control. Multilevel genome typing (MGT) with multiple levels of resolution has been previously demonstrated as a promising tool for this purpose. In this study, we developed MGT with nine levels for S. Enteritidis and characterised the genomic epidemiology of S. Enteritidis in detail. We examined 26 670 publicly available S. Enteritidis genome sequences from isolates spanning 101 years from 86 countries to reveal their spatial and temporal distributions. Using the lower resolution MGT levels, globally prevalent and regionally restricted sequence types (STs) were identified; avian associated MGT4-STs were found that were common in human cases in the USA; temporal trends were observed in the UK with MGT5-STs from 2014 to 2018 revealing both long lived endemic STs and the rapid expansion of new STs. Using MGT3 to MGT6, we identified multidrug resistance (MDR) associated STs at various MGT levels, which improves precision of detection and global tracking of MDR clones. We also found that the majority of the global S. Enteritidis population fell within two predominant lineages, which had significantly different propensity of causing large scale outbreaks. An online open MGT database has been established for unified international surveillance of S. Enteritidis. We demonstrated that MGT provides a flexible and high-resolution genome typing tool for S. Enteritidis surveillance and outbreak detection.
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  • 文章类型: Journal Article
    将成纤维细胞直接重编程为诱导心肌细胞(iCM)有望成为心血管疾病的潜在治疗方法。其中许多与功能性心肌细胞的巨大损失和瘢痕组织的同时形成有关。新兴的研究表明,引入三个最小的转录因子,Gata4,Mef2c,和Tbx5(G/M/T),可以将鼠成纤维细胞转化为在体外和体内与内源性CM非常相似的iCM。最近对iCM细胞命运决定的研究表明,去除遗传和表观遗传障碍可以促进iCM重编程。然而,研究小组之间不同的重编程效率阻碍了其进一步的研究和潜在的适用性。这里,我们提供了新的更新和详细的方案,用于使用编码G/M/T因子最佳表达的逆转录病毒多顺反子构建体从小鼠胚胎成纤维细胞和新生儿心脏成纤维细胞体外生成和评估功能性iCM。我们希望这个优化的协议将为未来小鼠iCM的机理研究和iCM生成的进一步改进奠定基础。
    Direct reprogramming of fibroblasts into induced cardiomyocytes (iCMs) holds great promise as a potential treatment for cardiovascular disease, many of which are associated with tremendous loss of functional cardiomyocytes and simultaneous formation of scar tissue. Burgeoning studies have shown that the introduction of three minimal transcriptional factors, Gata4, Mef2c, and Tbx5 (G/M/T), could convert murine fibroblasts into iCMs that closely resemble endogenous CMs both in vitro and in vivo. Recent studies on iCM cell fate determination have demonstrated that the removal of genetic and epigenetic barriers could facilitate iCM reprogramming. However, varied reprogramming efficiency among research groups hinders its further study and potential applicability. Here, we provide a newly updated and detailed protocol for in vitro generation and evaluation of functional iCMs from mouse embryonic fibroblasts and neonatal cardiac fibroblasts using retroviral polycistronic construct encoding optimal expression of G/M/T factors. We hope that this optimized protocol will lay the foundation for future mechanistic studies of murine iCMs and further improvement of iCM generation.
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  • 文章类型: Journal Article
    UNASSIGNED: At least eight MGT genes were identified in citrus and PtrMGT5 plays important role in maintaining Mg homeostasis in citrus by getting involved in the Mg absorption and transport. Magnesium (Mg) is an essential macronutrient for plant growth and development, and the magnesium transporter (MGT) genes participate in mediate Mg2+ uptake, translocation and sequestration into cellular storage compartments. Although several MGT genes have been characterized in various plant species, a comprehensive analysis of the MGT gene family in citrus is still uncharacterized. In this study, eight PtrMGT genes were identified through genome-wide analyses. Phylogenetic analyses revealed that PtrMGT genes were classified into five distinct subfamilies. A quantitative RT-PCR analysis showed that eight PtrMGT genes were expressed in all of the detected tissues and they mainly expressed in the vegetative organs. Expression analyses revealed the PtrMGT genes responded to various Mg deficiency stresses, including absolute Mg deficiency and antagonistic Mg deficiency which caused by low pH or Al toxicity. PtrMGT5, which localizes to the plasma membrane and was transcriptionally active, was functionally characterized. PtrMGT5 overexpression considerably enhanced absolute Mg deficiency and antagonistic Mg deficiency tolerance in transgenic Arabidopsis plants, which was accompanied by increased fresh weight and Mg content, whereas opposite changes were observed when PtrMGT5 homolog in Valencia Orange callus was knocked down. Taken together, PtrMGT5 plays important role in maintaining Mg homeostasis in citrus by getting involved in the Mg absorption and transport.
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  • 文章类型: Journal Article
    Direct reprogramming of fibroblasts into induced cardiomyocytes (iCMs) through forced expression of cardiac-lineage specific transcription factors holds promise as an alternative strategy for cardiac regeneration. To facilitate research in iCM reprogramming, we generated a suite of new tools. We developed a transformed cell line derived from mouse embryonic fibroblasts (MEF). This fibroblast cell line (MEF-T) harbors an αMHC-eGFP reporter transgene for rapid detection of newly derived iCMs. The MEF-T cell line is highly proliferative and easily transfected and transduced, making it an ideal tool for transgene expression and genetic manipulation. Additionally, we generated a Tet-On inducible polycistronic iCM reprogramming construct for the temporal regulation of reprogramming factor expression. Furthermore, we introduced this construct into MEF-T and created an inducible reprogrammable fibroblast cell line. These tools will facilitate future research in cell fate reprogramming by enabling the temporal control of reprogramming factor expression as well as high-throughput screening using libraries of small molecules, noncoding RNAs, and siRNAs. genesis 54:398-406, 2016. © 2016 Wiley Periodicals, Inc.
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  • 文章类型: Journal Article
    Chlamydia trachomatis (CT) is the most prevalent cause of sexually transmitted diseases. Although the prevalence of chlamydial infection is similar in men and women, current research and screening are still focused on women, who develop the most severe complications, leaving the study of male genital tract (MGT) infection underrated. Herein, we reviewed the literature on genital CT infection with special focus on the MGT. Data indicate that CT certainly infects different parts of the MGT such as the urethra, seminal vesicles, prostate, epididymis and testis. However, whether or not CT infection has detrimental effects on male fertility is still controversial. The most important features of CT infection are its chronic nature and the presence of a mild inflammation that remains subclinical in most individuals. Chlamydia antigens and pathogen recognition receptors (PRR), expressed on epithelial cells and immune cells from the MGT, have been studied in the last years. Toll-like receptor (TLR) expression has been observed in the testis, epididymis, prostate and vas deferens. It has been demonstrated that recognition of chlamydial antigens is associated with TLR2, TLR4, and possibly, other PRRs. CT recognition by PRRs induces a local production of cytokines/chemokines, which, in turn, provoke chronic inflammation that might evolve in the onset of an autoimmune process in genetically susceptible individuals. Understanding local immune response along the MGT, as well as the crosstalk between resident leukocytes, epithelial, and stromal cells, would be crucial in inducing a protective immunity, thus adding to the design of new therapeutic approaches to a Chlamydia vaccine.
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  • 文章类型: Journal Article
    BACKGROUND: The MediGuide technology (MGT) represents a novel sensor-based electromagnetic 4-dimensional (4D) navigation system allowing real-time catheter tracking in the environment of prerecorded X-ray loops.
    OBJECTIVE: To report on our clinical experience in atrial fibrillation (AF) ablation with recently available MGT-enabled ablation catheters.
    METHODS: The MGT was used in addition to a conventional 3D mapping system in 80 patients with AF (age 61 ± 10 years; 47 men; 40 with persistent AF), who underwent circumferential pulmonary vein isolation and voltage mapping with and without substrate modification. Short native right anterior oblique/left anterior oblique loops were used as background movies for the nonfluoroscopic placement of sensor-equipped diagnostic catheters into the coronary sinus and the right ventricle. After single transseptal puncture, selective angiograms of the pulmonary veins were used as background movies for near nonfluoroscopic left atrial reconstruction. Computed tomography registration as well as mapping/ablation was performed by using the new open-irrigated MGT-enabled ablation catheter.
    RESULTS: MGT application was not associated with a change in established workflow. Large parts of the procedure (mean entire duration 167 ± 47 minutes) could be done without additional fluoroscopy, whereas median residual fluoroscopy duration of 4.6 (interquartile range: 2.9, 7.1) minutes was mainly used for the acquisition of background loops, transseptal puncture, occasional verification of transseptal sheath position, and manipulation of the circular mapping catheter. Three (4%) minor complications occurred.
    CONCLUSIONS: The MGT integrates easily into the workflow of standard AF ablation and allows for high-quality nonfluoroscopic 4D catheter tracking. This results in low radiation exposure for patients and staff without complicating the workflow of the procedure.
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