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Association of growth performance and body conformational traits with BMP4 gene variation in Barki lambs Barki羔羊生长性能和身体构象特征与BMP4基因变异的关系
IF 1.8 4区 生物学 Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2019-07-04 DOI: 10.1080/08977194.2019.1662417
A. Ibrahim
Abstract The objective of this study was to test the association of the variation in a 360 bp region in exon 2 of the ovine bone morphogenetic protein 4 (BMP4) gene with growth performance (birth weight, pre-weaning average daily gain, weaning weight, post-weaning average daily gain and marketing weight) and body conformational traits (height at withers, height at hips, body length, heart girth, thigh circumference, body mass index, skeletal muscle index, body index and relative body index) in 242 Barki lambs using polymerase chain reaction-single strand conformational polymorphism (PCR-SSCP). Two variants (A and B) and three genotypes (AA, AB and BB) were detected. The BMP4 genotype significantly affected (p < .05 or p < .01) post-weaning daily gain, marketing weight, height at hips, thigh circumference, body mass index and skeletal muscle index. The results provided valuable information indicating selection for the BMP4 genotype might increase growth and muscularity in Barki lambs.
摘要本研究的目的是测试360 绵羊骨形态发生蛋白4(BMP4)基因外显子2的bp区与生长性能(出生体重、断奶前平均日增重、断奶体重、断奶后平均日增重和出栏体重)和身体构象特征采用聚合酶链反应-单链构象多态性(PCR-SSCP)对242只Barki羔羊进行了体长、腰围、大腿围、体重指数、骨骼肌指数、体指数和相对体指数的测定。检测到两种变体(A和B)和三种基因型(AA、AB和BB)。BMP4基因型显著影响(p<0.05或p<0.01)断奶后的日增重、上市体重、臀部高度、大腿周长、体重指数和骨骼肌指数。该结果提供了有价值的信息,表明BMP4基因型的选择可能会增加Barki羔羊的生长和肌肉发达程度。
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引用次数: 6
Plasma CCN2 is independently related to subsequent need for abdominal aorta aneurysm repair 血浆CCN2与随后腹主动脉动脉瘤修复的需要独立相关
IF 1.8 4区 生物学 Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2019-07-04 DOI: 10.1080/08977194.2019.1662416
J.H. Larsen, L. Rasmussen, J. Lindholt, L. Steffensen
Abstract The objective of this study was to determine if plasma CCN2 is associated with abdominal aorta aneurysm (AAA), and future need for AAA repair, and further to assess the potential clinical value of CCN2 in predicting disease outcome. CCN2 was quantified in plasma samples obtained from a cohort of 679 men aged 65–74 at initial ultrasound screening for AAA in the Viborg Vascular (VIVA) screening trial. Plasma CCN2 was correlated with need for future surgical repair in the whole study population (HR = 1.457 (1.081–1.962), p = .013) and in the AAA group alone (HR = 1.431 (1.064–1.926), p = .018), yet the predictive value (CCN2 > 0 and <0 of 0.52 and 0.55, respectively) disqualified its use in clinically relevant AAA repair prediction. In conclusion, CCN2 is independently related to subsequent need for AAA repair, but has negligible predictive power for clinical use.
摘要本研究的目的是确定血浆CCN2是否与腹主动脉瘤(AAA)有关,以及未来对AAA修复的需求,并进一步评估CCN2在预测疾病预后方面的潜在临床价值。在Viborg Vascular(VIVA)筛查试验中,从679名年龄在65-74岁之间的男性队列中获得的血浆样本中量化了CCN2。在整个研究人群中,血浆CCN2与未来手术修复的需求相关(HR=1.457(1.081–1.962),p = .013)和单纯AAA组(HR=1.431(1.064–1.926),p = .018),但是预测值(CCN2 > 分别为0.52和0.55的0和<0)不符合其在临床相关AAA修复预测中的应用。总之,CCN2与随后的AAA修复需求独立相关,但对临床应用的预测能力可忽略不计。
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引用次数: 0
Lowe syndrome with extremely short stature: growth hormone deficiency may be the pathogeny 身材极矮的洛氏综合征:生长激素缺乏可能是病因
IF 1.8 4区 生物学 Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2019-07-04 DOI: 10.1080/08977194.2019.1669589
C. Dai, Liying Wang, Youli Li, Zhichao Zheng, Jieqi Qian, Chaoban Wang, Zishuo Liu, Xiaoou Shan
Abstract Lowe syndrome is an x-linked disorder characterized by congenital cataracts, nervous system abnormalities and renal tubular dysfunction. With the rising number of reported cases, more patients are found to suffer from endocrine abnormalities. Hereby, three Chinese patients with typical symptoms and extremely short stature were described. The OCRL gene was analyzed. A combination of blood biochemistry and radiological examinations were performed. Growth hormone provocation test was taken in one patient. Nucleotide sequence analysis revealed a de novo novel hemizygous mutation (c.2290_2291delinsCT) in exon 21 in an adolescent boy. As indicated by the growth hormone provocation test, the boy had growth hormone deficiency. The other two patients were brothers with extremely short stature, and manifested the same hemizygous mutation (c.2581G > A) in exon 23. It was speculated that the mutation of OCRL gene could lead to deficiency of growth hormone, for which an early growth hormone intervention may be beneficial.
摘要Lowe综合征是一种以先天性白内障、神经系统异常和肾小管功能障碍为特征的x连锁疾病。随着报告病例数量的增加,越来越多的患者被发现患有内分泌异常。在此,对三名症状典型、身材矮小的中国患者进行了描述。对OCRL基因进行了分析。结合血液生化和放射学检查。对一名患者进行了生长激素激发试验。核苷酸序列分析显示,在一名青春期男孩的外显子21中出现了一个新的半合子突变(c.2290_2291DelisCT)。生长激素激发试验表明,男孩生长激素缺乏。另外两名患者是身材极短的兄弟,表现出相同的半合子突变(约2581G > A) 在外显子23中。推测OCRL基因突变可能导致生长激素缺乏,早期生长激素干预可能是有益的。
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引用次数: 2
Dose optimisation of PTEN inhibitor, bpV (HOpic), and SCF for the in-vitro activation of sheep primordial follicles PTEN抑制剂bpV(HOpic)和SCF体外激活绵羊原始卵泡的剂量优化
IF 1.8 4区 生物学 Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2019-07-04 DOI: 10.1080/08977194.2019.1680661
S. Adib, M. R. Valojerdi, M. Alikhani
Abstract The in-vitro development of primordial follicles is critical for improving mammalian fertility and wildlife conservation. This study aimed to optimise the effective doses of bpV (HOpic) and stem cell factor (SCF) for the in-vitro activation of sheep primordial follicles. To do this, sheep ovarian cortex was treated with bpV (1.5, 15, and 150 μM) and SCF (50 and 100 ng/ml). Follicular count indicated that 15 μM bpV and 100 ng/ml SCF significantly increased normal primary follicles compared to other groups (p < 0.05). Also, a significant downregulation of P53 and PTEN, as well as the increased expression of PI3K was observed. The in-vitro maturation was more pronounced when the fragmented tissues were co-treated with selected doses of bpV and SCF. In conclusion, the combination of 15 μM bpV and 100 ng/ml SCF was the most effective treatment strategy for the activation and survival of primordial follicles in sheep ovarian fragments.
摘要原始卵泡的体外发育对提高哺乳动物的生育能力和野生动物保护至关重要。本研究旨在优化体外激活绵羊原始卵泡的bpV(HOpic)和干细胞因子(SCF)的有效剂量。为此,绵羊卵巢皮质接受bpV(1.5、15和150 μM)和SCF(50和100 ng/ml)。卵泡计数显示15 μM bpV和100 与其他组相比,ng/ml SCF显著增加了正常初级卵泡(p < 0.05)。此外,观察到P53和PTEN的显著下调以及PI3K的表达增加。当用选定剂量的bpV和SCF共同处理碎片组织时,体外成熟更加明显。总之,15 μM bpV和100 ng/ml SCF是绵羊卵巢碎片中原始卵泡活化和存活最有效的治疗策略。
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引用次数: 13
Recombinant protein CCN5/WISP2 promotes islet cell proliferation and survival in vitro 重组蛋白CCN5/WISP2促进胰岛细胞体外增殖和存活
IF 1.8 4区 生物学 Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2019-07-04 DOI: 10.1080/08977194.2019.1652400
Nancy Kaddour, Di Zhang, Zu-hua Gao, Jun-li Liu
Abstract Pancreatic ß cell proliferation, survival and function are key elements that need to be considered in developing novel antidiabetic therapies. We recently identified CCN5/WISP2 to have potential growth promoting properties when overexpressed in ß cells; however, further investigations are needed to validate those properties. In this study, we demonstrated that exogenous treatment of insulinoma cells and primary islets with recombinant CCN5 (rh-CCN5) protein enhanced the proliferative capacity which was correlated with activation of cell-cycle regulators CDK4 and cyclin D1. Furthermore, pre-incubation of these cells with rh-CCN5 enhanced their survival rate after being exposed to harsh treatments such as streptozotocin and high concentrations of glucose and free fatty acids. CCN5 as well caused an upregulation in the expression of key genes associated with ß cell identity and function such as GLUT-2 and GCK. Finally, CCN5 activated FAK and downstream ERK kinases which are known to stimulate cell proliferation and survival. Hence, our results validate the growth promoting activities of rh-CCN5 in ß cells and open the door for further investigations in vivo.
胰腺细胞的增殖、存活和功能是开发新型降糖疗法需要考虑的关键因素。我们最近发现CCN5/WISP2在ß细胞中过表达时具有潜在的促进生长的特性;然而,需要进一步的调查来验证这些特性。在这项研究中,我们证明了用重组CCN5 (rh-CCN5)蛋白外源性处理胰岛素瘤细胞和原代胰岛增强了增殖能力,这与细胞周期调节因子CDK4和细胞周期蛋白D1的激活有关。此外,用rh-CCN5对这些细胞进行预孵育,可以提高它们在暴露于链脲佐菌素和高浓度葡萄糖和游离脂肪酸等严酷处理后的存活率。CCN5还引起与ß细胞身份和功能相关的关键基因如GLUT-2和GCK的表达上调。最后,CCN5激活FAK和下游ERK激酶,已知它们能刺激细胞增殖和存活。因此,我们的研究结果验证了rh-CCN5在ß细胞中的促生长活性,并为进一步的体内研究打开了大门。
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引用次数: 6
Growth factor signaling pathways in vascular development and disease. 血管发育和疾病中的生长因子信号通路。
IF 1.8 4区 生物学 Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2019-04-01 Epub Date: 2019-07-08 DOI: 10.1080/08977194.2019.1635591
Zoe L Grant, Leigh Coultas

Angiogenic blood vessel growth is essential to ensure organs receive adequate blood supply to support normal organ function and homeostasis. Angiogenesis involves a complex series of cellular events through which new vessels grow out from existing vasculature. Growth factor signaling, layered over a range of other signaling inputs, orchestrates this process. The response of endothelial cells (ECs) to growth factor signals must be carefully controlled through feedback mechanisms to prevent excessive vessel growth, remodeling or destabilization. In this article, we summarize recent findings describing how ECs respond to growth factor signals during blood vessel development and homeostasis and how perturbation of these responses can lead to disease.

血管生成的血管生长对于确保器官获得足够的血液供应以支持正常的器官功能和体内平衡至关重要。血管生成涉及一系列复杂的细胞事件,通过这些事件,新的血管从现有的血管系统中生长出来。生长因子信号在一系列其他信号输入上分层,协调了这一过程。内皮细胞(ECs)对生长因子信号的反应必须通过反馈机制仔细控制,以防止过度的血管生长、重塑或不稳定。在本文中,我们总结了最近的研究结果,描述了内皮细胞在血管发育和体内平衡过程中如何响应生长因子信号,以及这些反应的扰动如何导致疾病。
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引用次数: 8
Emerging roles for Interleukin-11 in disease. 白细胞介素-11在疾病中的新作用。
IF 1.8 4区 生物学 Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2019-04-01 Epub Date: 2019-06-04 DOI: 10.1080/08977194.2019.1620227
Paul M Nguyen, Suad M Abdirahman, Tracy L Putoczki

Interleukin (IL)-11 belongs to the IL-6 family of cytokines, discovered over 30 years ago. While early studies focused on the ability of IL-11 to stimulate megakaryocytopoiesis, the importance of this cytokine to inflammatory disease and cancers is only just beginning to be uncovered. This review outlines recent advances in our understanding of IL-11 biology, and highlights the development of novel therapeutics with the potential for clinical targeting of signaling by this cytokine in multiple diseases.

白细胞介素(IL)-11属于IL-6细胞因子家族,发现于30多年前。虽然早期的研究集中在IL-11刺激巨核细胞生成的能力上,但这种细胞因子对炎症性疾病和癌症的重要性才刚刚开始被发现。本文概述了我们对IL-11生物学的最新理解,并强调了在多种疾病中具有临床靶向这种细胞因子信号传导潜力的新治疗方法的发展。
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引用次数: 26
Bone morphogenetic protein signaling in breast cancer progression. 乳腺癌进展中的骨形态发生蛋白信号。
IF 1.8 4区 生物学 Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2019-04-01 Epub Date: 2019-07-05 DOI: 10.1080/08977194.2019.1626378
Lap Hing Chi, Allan D Burrows, Robin L Anderson

Breast cancer is the most prevalent type of cancer amongst women worldwide. The mortality rate for patients with early-stage breast cancer has been decreasing, however, the 5-year survival rate for patients with metastatic disease remains poor, currently at 27%. Here, we have reviewed the current understanding of the role of bone morphogenetic protein (BMP) signaling in breast cancer progression, and have highlighted the discordant results that are reported in different studies. We propose that some of these contradictory outcomes may result from signaling through either the canonical or non-canonical pathways in different cell lines and tumors, or from different tumor-stromal interactions that occur in vivo.

乳腺癌是全世界女性中最常见的癌症类型。早期乳腺癌患者的死亡率一直在下降,然而,转移性疾病患者的5年生存率仍然很低,目前为27%。在这里,我们回顾了目前对骨形态发生蛋白(BMP)信号在乳腺癌进展中的作用的理解,并强调了不同研究中报道的不一致结果。我们认为,这些相互矛盾的结果可能是由于信号通过不同细胞系和肿瘤的典型或非典型途径,或者来自体内发生的不同肿瘤-基质相互作用。
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引用次数: 9
Hepatocyte growth factor levels in livers and serum at Kasai-portoenterostomy are not predictive of clinical outcome in infants with biliary atresia. kasai门肠造口术患者肝脏和血清中的肝细胞生长因子水平不能预测胆道闭锁婴儿的临床结果。
IF 1.8 4区 生物学 Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2019-04-01 Epub Date: 2019-06-11 DOI: 10.1080/08977194.2019.1626379
Omid Madadi-Sanjani, Joachim F Kuebler, Stephanie Dippel, Anna Gigina, Christine S Falk, Gertrud Vieten, Claus Petersen, Christian Klemann

Biliary atresia (BA) is characterized by progressive destruction of the biliary system leading to liver fibrosis and deterioration of liver function. Serum hepatocyte growth factor (HGF) has been shown to be increased in cirrhotic diseases including BA. The aim of this study was to investigate the prognostic value of HGF levels in sera and liver tissue for the further disease course. A total of 49 serum and liver samples from infants with BA were acquired during Kasai-portoenterostomy (KPE) and analyzed by multiplex immunoassay including HGF, as marker of liver regeneration, and Interleukin 6 (IL-6) as a marker of inflammation. Both mediators showed no correlation with the outcome defined as favorable (survival with native liver (SNL)) or, in contrast, rapid deterioration of liver function requiring transplantation. Our data suggest that the degree of liver regeneration indicated by high levels of HGF within the liver is a dismissible factor in the post-KPE disease course.

胆道闭锁(BA)的特点是胆道系统的进行性破坏,导致肝纤维化和肝功能恶化。血清肝细胞生长因子(HGF)已被证明在包括BA在内的肝硬化疾病中升高。本研究的目的是探讨血清和肝组织中HGF水平对进一步病程的预后价值。在kasai门肠造口术(KPE)中采集了49份BA婴儿的血清和肝脏样本,并进行了多重免疫分析,包括肝再生标志物HGF和炎症标志物白细胞介素6 (IL-6)。两种介质均未显示出与预后(原生肝存活(SNL))或肝功能快速恶化(需要移植)相关。我们的数据表明,肝脏内高水平HGF所表明的肝脏再生程度是kpe后疾病过程中不可忽视的因素。
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引用次数: 2
Structure, function and disease relevance of Wnt inhibitory factor 1, a secreted protein controlling the Wnt and hedgehog pathways. Wnt抑制因子1(一种控制Wnt和hedgehog通路的分泌蛋白)的结构、功能和疾病相关性
IF 1.8 4区 生物学 Q4 Biochemistry, Genetics and Molecular Biology Pub Date : 2019-04-01 Epub Date: 2019-06-18 DOI: 10.1080/08977194.2019.1626380
Krisztina Kerekes, László Bányai, Mária Trexler, László Patthy

Wnts and Hedgehogs (Hh) are large, lipid-modified extracellular morphogens that play key roles in embryonic development and stem cell proliferation of Metazoa. Both morphogens signal through heptahelical Frizzled-type receptors of the G-Protein Coupled Receptor family and there are several other similarities that suggest a common evolutionary origin of the Hh and Wnt pathways. There is evidence that the secreted protein, Wnt inhibitory factor 1 (WIF1) modulates the activity of both Wnts and Hhs and may thus contribute to the intertwining of these pathways. In this article, we review the structure, evolution, molecular interactions and functions of WIF1 with major emphasis on its role in carcinogenesis.

wnt和刺猬(Hh)是大的、脂质修饰的细胞外形态因子,在后生动物的胚胎发育和干细胞增殖中起关键作用。这两种形态因子都通过g蛋白偶联受体家族的七螺旋卷曲型受体发出信号,还有其他一些相似之处表明Hh和Wnt途径具有共同的进化起源。有证据表明,分泌蛋白Wnt抑制因子1 (WIF1)调节Wnt和Hhs的活性,从而可能促进这些途径的交织。在本文中,我们综述了WIF1的结构、进化、分子相互作用和功能,重点介绍了它在致癌中的作用。
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引用次数: 13
期刊
Growth factors
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