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An integrative multiscale view of early cardiac looping. 早期心脏循环的综合多尺度视角。
IF 3.1 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2022-01-01 Epub Date: 2021-08-13 DOI: 10.1002/wsbm.1535
Nazanin Ebrahimi, Christopher Bradley, Peter Hunter

The heart is the first organ to form and function during the development of an embryo. Heart development consists of a series of events believed to be highly conserved in vertebrates. Development of heart begins with the formation of the cardiac fields followed by a linear heart tube formation. The straight heart tube then undergoes a ventral bending prior to further bending and helical torsion to form a looped heart. The looping phase is then followed by ballooning, septation, and valve formation giving rise to a four-chambered heart in avians and mammals. The looping phase plays a central role in heart development. Successful looping is essential for proper alignment of the future cardiac chambers and tracts. As aberrant looping results in various congenital heart diseases, the mechanisms of cardiac looping have been studied for several decades by various disciplines. Many groups have studied anatomy, biology, genetics, and mechanical processes during heart looping, and have proposed multiple mechanisms. Computational modeling approaches have been utilized to examine the proposed mechanisms of the looping process. Still, the exact underlying mechanism(s) controlling the looping phase remain poorly understood. Although further experimental measurements are obviously still required, the need for more integrative computational modeling approaches is also apparent in order to make sense of the vast amount of experimental data and the complexity of multiscale developmental systems. Indeed, there needs to be an iterative interaction between experimentation and modeling in order to properly find the gap in the existing data and to validate proposed hypotheses. This article is categorized under: Cardiovascular Diseases > Genetics/Genomics/Epigenetics Cardiovascular Diseases > Computational Models Cardiovascular Diseases > Molecular and Cellular Physiology.

心脏是胚胎发育过程中最先形成并发挥作用的器官。心脏发育由一系列被认为在脊椎动物中高度保守的事件组成。心脏的发育始于心场的形成,随后是线性心管的形成。直心管在进一步弯曲和螺旋扭转之前经历腹侧弯曲,形成环状心脏。环状阶段之后是膨胀、分隔和瓣膜形成,最终形成鸟类和哺乳动物的四腔心脏。循环期在心脏发育中起着核心作用。成功的环袢对于未来的心腔和心束的正确排列至关重要。作为各种先天性心脏病的异常环,各学科对心脏环的机制已经进行了几十年的研究。许多研究小组研究了心脏循环的解剖学、生物学、遗传学和机械过程,并提出了多种机制。计算建模方法已被用来检查提出的机制的循环过程。然而,控制循环阶段的确切潜在机制仍然知之甚少。虽然显然还需要进一步的实验测量,但为了理解大量的实验数据和多尺度发育系统的复杂性,对更综合的计算建模方法的需求也很明显。事实上,为了正确地找到现有数据中的差距并验证提出的假设,在实验和建模之间需要进行迭代交互。本文分类如下:心血管疾病>遗传学/基因组学/表观遗传学心血管疾病>计算模型心血管疾病>分子和细胞生理学。
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引用次数: 0
Seven challenges in the multiscale modeling of multicellular tissues. 多细胞组织多尺度建模的七大挑战。
IF 4.6 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2022-01-01 Epub Date: 2021-05-04 DOI: 10.1002/wsbm.1527
Alexander G Fletcher, James M Osborne

The growth and dynamics of multicellular tissues involve tightly regulated and coordinated morphogenetic cell behaviors, such as shape changes, movement, and division, which are governed by subcellular machinery and involve coupling through short- and long-range signals. A key challenge in the fields of developmental biology, tissue engineering and regenerative medicine is to understand how relationships between scales produce emergent tissue-scale behaviors. Recent advances in molecular biology, live-imaging and ex vivo techniques have revolutionized our ability to study these processes experimentally. To fully leverage these techniques and obtain a more comprehensive understanding of the causal relationships underlying tissue dynamics, computational modeling approaches are increasingly spanning multiple spatial and temporal scales, and are coupling cell shape, growth, mechanics, and signaling. Yet such models remain challenging: modeling at each scale requires different areas of technical skills, while integration across scales necessitates the solution to novel mathematical and computational problems. This review aims to summarize recent progress in multiscale modeling of multicellular tissues and to highlight ongoing challenges associated with the construction, implementation, interrogation, and validation of such models. This article is categorized under: Reproductive System Diseases > Computational Models Metabolic Diseases > Computational Models Cancer > Computational Models.

多细胞组织的生长和动态涉及严格调控和协调的形态发生细胞行为,如形状变化、运动和分裂,这些行为受亚细胞机制支配,并通过短程和远程信号耦合。发育生物学、组织工程学和再生医学领域面临的一个关键挑战是了解不同尺度之间的关系如何产生新的组织尺度行为。分子生物学、活体成像和体内外技术的最新进展彻底改变了我们通过实验研究这些过程的能力。为了充分利用这些技术,并更全面地了解组织动力学的因果关系,计算建模方法越来越多地跨越多个空间和时间尺度,并将细胞形状、生长、力学和信号传递结合起来。然而,这些模型仍然具有挑战性:每个尺度的建模需要不同领域的技术技能,而跨尺度的整合则需要解决新的数学和计算问题。这篇综述旨在总结多细胞组织多尺度建模的最新进展,并强调与此类模型的构建、实施、查询和验证相关的持续挑战。本文归类于生殖系统疾病 > 计算模型 代谢性疾病 > 计算模型 癌症 > 计算模型。
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引用次数: 0
Transferability of tigecycline resistance: Characterization of the expanding Tet(X) family. 替加环素耐药性的可转移性:扩展Tet(X)家族的表征。
IF 3.1 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2022-01-01 Epub Date: 2021-10-05 DOI: 10.1002/wsbm.1538
Chao-Yue Cui, Qiwei Chen, Qian He, Chong Chen, Rong-Min Zhang, Youjun Feng, Jian Sun

Tetracycline and its derivative tigecycline are clinical options against Gram-negative bacterial infections. The emergence of mobile Tet(X) enzymes that destruct tetracycline-type antibiotics is posing a big challenge to antibacterial therapy and food/environmental securities. Here, we present an update on a growing number of Tet(X) variants. We describe structure and action of Tet(X) enzyme, and discuss the evolutional origin. In addition, potential Tet(X) inhibitors are given. This mini-review might benefit better understanding of Tet(X)-mediated tigecycline resistance. This article is categorized under: Infectious Diseases > Genetics/Genomics/Epigenetics Infectious Diseases > Environmental Factors Infectious Diseases > Molecular and Cellular Physiology.

四环素及其衍生物替加环素是治疗革兰氏阴性细菌感染的临床选择。破坏四环素类抗生素的移动Tet(X)酶的出现对抗菌治疗和食品/环境安全提出了重大挑战。在这里,我们介绍了越来越多的Tet(X)变体的最新情况。介绍了Tet(X)酶的结构和作用,并讨论了其进化起源。此外,还给出了潜在的Tet(X)抑制剂。这项小型综述可能有助于更好地了解Tet(X)介导的替加环素耐药性。本文分类为:传染病>遗传学/基因组学/表观遗传学>环境因素传染病>分子与细胞生理学。
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引用次数: 5
Issue Information 问题信息
IF 3.1 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2022-01-01 DOI: 10.1002/wsbm.1528
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引用次数: 0
Immunohistochemical evidence for adult human neurogenesis in health and disease. 成人神经发生在健康和疾病中的免疫组织化学证据。
IF 3.1 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2021-11-01 Epub Date: 2021-04-01 DOI: 10.1002/wsbm.1526
Natalie Gault, Francis G Szele

Postnatal and adult neurogenesis in the subventricular zone and subgranular zone of animals such as rodents and non-human primates has been observed with many different technical approaches. Since most techniques used in animals cannot be used in humans, the majority of human neurogenesis studies rely on postmortem immunohistochemistry. This technique is difficult in human tissue, due to poor and variable preservation of antigens and samples. Nevertheless, a survey of the literature reveals that most published studies provide evidence for childhood and adult neurogenesis in the human brain stem cell niches. There are some conflicting results even when assessing the same markers and when using the same antibodies. Focusing on immunohistochemical studies on post-mortem human sections, we discuss the relative robustness of the literature on adult neurogenesis. We also discuss the response of the subventricular and subgranular zones to human disease, showing that the two niches can respond differently and that the stage of disease impacts neurogenesis levels. Thus, we highlight strong evidence for adult human neurogenesis, discuss other work that did not find it, describe obstacles in analysis, and offer other approaches to evaluate the neurogenic potential of the subventricular and subgranular zones of Homo sapiens. This article is categorized under: Neurological Diseases > Stem Cells and Development Reproductive System Diseases > Stem Cells and Development.

在动物如啮齿动物和非人灵长类动物的脑室下区和颗粒下区,已经用许多不同的技术方法观察到出生后和成年后的神经发生。由于大多数用于动物的技术不能用于人类,因此大多数人类神经发生研究依赖于死后免疫组织化学。这种技术在人体组织中是困难的,因为抗原和样本的保存很差,而且变化无常。然而,一项文献调查显示,大多数已发表的研究都提供了儿童和成人脑干细胞龛神经发生的证据。即使在评估相同的标记物和使用相同的抗体时,也会出现一些相互矛盾的结果。聚焦于死后人体切片的免疫组织化学研究,我们讨论了成人神经发生文献的相对稳健性。我们还讨论了脑室下区和颗粒下区对人类疾病的反应,表明这两个生态位可以有不同的反应,疾病的阶段影响神经发生水平。因此,我们强调了成年人神经发生的有力证据,讨论了其他没有发现它的工作,描述了分析中的障碍,并提供了其他方法来评估智人脑室下和亚颗粒带的神经发生潜力。本文分类如下:神经系统疾病>干细胞与发育生殖系统疾病>干细胞与发育。
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引用次数: 8
Computational anatomy and diffeomorphometry: A dynamical systems model of neuroanatomy in the soft condensed matter continuum. 计算解剖学和微分形态学:软凝聚态连续体中神经解剖学的动力系统模型。
IF 3.1 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2021-11-01 Epub Date: 2021-03-24 DOI: 10.1002/wsbm.1524
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引用次数: 1
Diversity of bet‐hedging strategies in microbial communities—Recent cases and insights 微生物群落下注对冲策略的多样性-最近的案例和见解
IF 3.1 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2021-11-01 DOI: 10.1002/wsbm.1544
L. Morawska, Jhonatan A. Hernandez-Valdes, O. Kuipers
Abstract Microbial communities are continuously exposed to unpredictable changes in their environment. To thrive in such dynamic habitats, microorganisms have developed the ability to readily switch phenotypes, resulting in a number of differently adapted subpopulations expressing various traits. In evolutionary biology, a particular case of phenotypic heterogeneity that evolved in an unpredictably changing environment has been defined as bet‐hedging. Bet‐hedging is a risk‐spreading strategy where isogenic populations stochastically (randomly) diversify their phenotypes, often resulting in maladapted individuals that suffer lower reproductive success. This fitness trade‐off in a specific environment may have a selective advantage upon the sudden environmental shift. Thus, a bet‐hedging strategy allows populations to persist in very dynamic habitats, but with a particular fitness cost. In recent years, numerous examples of phenotypic heterogeneity in different microorganisms have been observed, some suggesting bet‐hedging. Here, we highlight the latest reports concerning bet‐hedging phenomena in various microorganisms to show how versatile this strategy is within the microbial realms. This article is categorized under: Infectious Diseases > Molecular and Cellular Physiology
摘要微生物群落不断地暴露在环境中不可预测的变化中。为了在这种动态的栖息地中茁壮成长,微生物已经发展出了容易转换表型的能力,从而产生了许多不同适应的亚群,表达各种特征。在进化生物学中,在不可预测的变化环境中进化的表型异质性的特殊情况被定义为赌注对冲。赌注对冲是一种风险传播策略,同基因群体随机(随机)使其表型多样化,通常导致不适应的个体生殖成功率较低。这种在特定环境中的适应性权衡可能在环境突然变化时具有选择性优势。因此,赌注对冲策略允许种群在非常动态的栖息地中生存,但需要特定的适应成本。近年来,在不同的微生物中观察到了许多表型异质性的例子,其中一些表明了赌注对冲。在这里,我们重点介绍了有关各种微生物中赌注对冲现象的最新报告,以显示这种策略在微生物领域中的多功能性。这篇文章分类在:传染病>分子和细胞生理学
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引用次数: 15
Tumor models in various Drosophila tissues. 果蝇各种组织中的肿瘤模型。
IF 3.1 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2021-11-01 Epub Date: 2021-03-21 DOI: 10.1002/wsbm.1525
Shangyu Gong, Yichi Zhang, Aiguo Tian, Wu-Min Deng

The development of cancer is a complex multistage process. Over the past few decades, the model organism Drosophila melanogaster has been crucial in identifying cancer-related genes and pathways and elucidating mechanisms underlying growth regulation in development. Investigations using Drosophila has yielded new insights into the molecular mechanisms involved in tumor initiation and progression. In this review, we describe various tumor models that have been developed in recent years using different Drosophila tissues, such as the imaginal tissue, the neural tissue, the gut, the ovary, and hematopoietic cells. We discuss underlying genetic alterations, cancer-like characteristics, as well as similarities and key differences among these models. We also discuss how disruptions in stem cell division and differentiation result in tumor formation in diverse tissues, and highlight new concepts developed using the fly model to understand context-dependent tumorigenesis. We further discuss the progress made in Drosophila to explore tumor-host interactions that involve the innate immune response to tumor growth and the cachexia wasting phenotype. This article is categorized under: Cancer > Genetics/Genomics/Epigenetics Cancer > Stem Cells and Development Cancer > Molecular and Cellular Physiology.

癌症的发生发展是一个复杂的多阶段过程。过去几十年来,黑腹果蝇这一模式生物在鉴定癌症相关基因和途径以及阐明发育过程中的生长调控机制方面发挥了至关重要的作用。利用果蝇进行的研究对肿瘤发生和发展的分子机制有了新的认识。在这篇综述中,我们介绍了近年来利用果蝇的不同组织(如想象组织、神经组织、肠道、卵巢和造血细胞)建立的各种肿瘤模型。我们将讨论这些模型的潜在基因改变、类癌特征以及相似之处和主要差异。我们还讨论了干细胞分裂和分化紊乱如何导致肿瘤在不同组织中形成,并重点介绍了利用蝇类模型理解肿瘤发生的环境依赖性的新概念。我们进一步讨论了果蝇在探索肿瘤-宿主相互作用方面取得的进展,这种相互作用涉及对肿瘤生长的先天免疫反应和恶病质消瘦表型。本文归类于癌症 > 遗传学/基因组学/表观遗传学 癌症 > 干细胞与发育 癌症 > 分子与细胞生理学。
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引用次数: 0
Fluid mechanical modeling of the upper urinary tract. 上尿路的流体力学模型。
IF 3.1 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2021-11-01 Epub Date: 2021-03-14 DOI: 10.1002/wsbm.1523
Shaokai Zheng, Dario Carugo, Ali Mosayyebi, Ben Turney, Fiona Burkhard, Dirk Lange, Dominik Obrist, Sarah Waters, Francesco Clavica

The upper urinary tract (UUT) consists of kidneys and ureters, and is an integral part of the human urogenital system. Yet malfunctioning and complications of the UUT can happen at all stages of life, attributed to reasons such as congenital anomalies, urinary tract infections, urolithiasis and urothelial cancers, all of which require urological interventions and significantly compromise patients' quality of life. Therefore, many models have been developed to address the relevant scientific and clinical challenges of the UUT. Of all approaches, fluid mechanical modeling serves a pivotal role and various methods have been employed to develop physiologically meaningful models. In this article, we provide an overview on the historical evolution of fluid mechanical models of UUT that utilize theoretical, computational, and experimental approaches. Descriptions of the physiological functionality of each component are also given and the mechanical characterizations associated with the UUT are provided. As such, it is our aim to offer a brief summary of the current knowledge of the subject, and provide a comprehensive introduction for engineers, scientists, and clinicians who are interested in the field of fluid mechanical modeling of UUT. This article is categorized under: Cancer > Biomedical Engineering Infectious Diseases > Biomedical Engineering Reproductive System Diseases > Biomedical Engineering.

上尿路(UUT)由肾脏和输尿管组成,是人类泌尿生殖系统的一个组成部分。然而,由于先天性异常、尿路感染、尿石症和尿路上皮癌等原因,UUT的功能障碍和并发症可能发生在生命的各个阶段,所有这些都需要泌尿外科干预,并严重影响患者的生活质量。因此,已经开发了许多模型来解决UUT的相关科学和临床挑战。在所有方法中,流体力学建模起着关键作用,各种方法被用来开发有生理学意义的模型。在这篇文章中,我们概述了利用理论、计算和实验方法的UUT流体力学模型的历史演变。还给出了每个组件的生理功能的描述,并提供了与UUT相关的机械特性。因此,我们的目标是对该主题的当前知识进行简要总结,并为对UUT流体力学建模领域感兴趣的工程师,科学家和临床医生提供全面的介绍。本文分类如下:癌症>生物医学工程传染病>生物医学工程生殖系统疾病>生物医学工程。
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引用次数: 14
Trained immunity in the mucosal diseases. 在粘膜疾病中训练免疫力。
IF 3.1 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2021-10-27 DOI: 10.1002/wsbm.1543
Dou Yu, Jiaqi Zhang, Shuo Wang
Immune memory is well known as a signature of the adaptive immune system. Recently, enhanced responses to subsequent triggers are also observed in innate immune system, termed trained immunity (TI). Awakening of innate immune memory is required for host defense, such as anti-pathogen and anti-tumor responses. However, hyper-reactivation of trained innate immune cells also gives rise to undesirable inflammation. Mucosa immune system serves as the first defense line against pathogens. Trained immunity of mucosal immune system is tightly associated with the outcomes of mucosal diseases. In this review, we discuss the role of trained immunity in mucosal-associated diseases and the underlying mechanisms. We summarize the metabolic and epigenetic changes of trained immune cells and highlight their potential in clinical treatment. This article is categorized under: Infectious Diseases > Molecular and Cellular Physiology.
众所周知,免疫记忆是适应性免疫系统的特征。最近,在先天免疫系统中也观察到对随后触发的反应增强,称为训练免疫(TI)。宿主防御需要唤醒先天免疫记忆,如抗病原体和抗肿瘤反应。然而,经过训练的先天免疫细胞的过度再激活也会引起不良炎症。粘膜免疫系统是抵御病原体的第一道防线。粘膜免疫系统的训练免疫与粘膜疾病的结果密切相关。在这篇综述中,我们讨论了训练免疫在粘膜相关疾病中的作用及其潜在机制。我们总结了经过训练的免疫细胞的代谢和表观遗传学变化,并强调了它们在临床治疗中的潜力。这篇文章分类在:传染病>分子和细胞生理学。
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引用次数: 2
期刊
WIREs Mechanisms of Disease
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