Modeling specific aneuploidies: from karyotype manipulations to biological insights

An abnormal chromosome number, or aneuploidy, underlies developmental disorders and is a common feature of cancer, with different cancer types exhibiting distinct patterns of chromosomal gains and losses. To understand how specific aneuploidies emerge in certain tissues and how they contribute to disease development, various methods have been developed to alter the karyotype of mammalian cells and mice. In this review, we provide an overview of both classic and novel strategies for inducing or selecting specific chromosomal gains and losses in human and murine cell systems. We highlight how these customized aneuploidy models helped expanding our knowledge of the consequences of specific aneuploidies to (cancer) cell physiology

A kinesin-based approach for inducing chromosome-specific mis-segregation in human cells

Various cancer types exhibit characteristic and recurrent aneuploidy patterns. The origins of these cancer type-specific karyotypes are still unknown, partly because introducing or eliminating specific chromosomes in human cells still poses a challenge. Here, we describe a novel strategy to induce mis-segregation of specific chromosomes in different human cell types. We employed Tet repressor or nuclease-dead Cas9 to link a microtubule minus-end-directed kinesin (Kinesin14VIb) from Physcomitrella patens to integrated Tet operon repeats and chromosome-specific endogenous repeats, respectively. By live- and fixed-cell imaging, we observed poleward movement of the targeted loci during (pro)metaphase. Kinesin14VIb-mediated pulling forces on the targeted chromosome were counteracted by forces from kinetochore-attached microtubules. This tug-of-war resulted in chromosome-specific segregation errors during anaphase and revealed that spindle forces can heavily stretch chromosomal arms. By single-cell whole-genome sequencing, we established that kinesin-induced targeted mis-segregations predominantly result in chromosomal arm aneuploidies after a single cell division. Our kinesin-based strategy opens the possibility to investigate the immediate cellular responses to specific aneuploidies in different cell types; an important step toward understanding how tissue-specific aneuploidy patterns evolve.</p

HMU fluorinze mouthwash enhances enamel remineralization: An in vitro study

BACKGROUND: Fluoride therapy has long been used extensively to prevent dental caries. Fluoride appears in variety of dental care products such as mouthrinse, dentifrice, gel, etc. HMU fluorinze is the first mouthwash containing fluoride in Vietnam. AIM: This research was conducted to evaluate the efficacy of HMU Fluorinze mouthwash on remineralizing enamel in laboratory conditions. METHODS: 20 third molars teeth were cleaned and covered with nail polish , except for a 3x3 mm square on their buccal surfaces. These teeth went through two steps: demineralization using Coke and remineralization for 20 days: 1) using standard calcifying solution (control group) and 2) using standard calcifying solution + HMU Fluorinze mouthwash 2 times/day (experimental group). The mineralization index of enamel structure after demineralization and remineralization was assessed by DIAGNOdent pen 2190. RESULTS: The mineralization indexes of the control group and experimental group at baseline were 3.65 ± 0.76 and 3.35 ± 0.64, after demineralization were in turn of 21.78 ± 4.48 and 20.25 ± 2.26; and after remineralization were 6.30 ± 1.03 and 3.90 ± 1.24. The different figures &nbsp;between the two groups after remineralization shows statistical significance (p&lt;0.01). Group B using HMU fluorinze mouthwash after 20 days did not differ from the original results (p = 0.272), in contrast with the control group (p&lt;0.01). CONCLUSIONS: HMU fluorinze mouthwash has better mineralization effect than standard calcifying solution

ẢNH HƯỞNG CỦA CÔNG NGHỆ THỰC TẾ ẢO TĂNG CƯỜNG ĐẾN Ý ĐỊNH MUA HÀNG TRỰC TUYẾN CỦA NGƯỜI TIÊU DÙNG

The study shows the effects of factors affecting consumers' purchase intention after experiencing Virtual Try-on (VTO) in Vietnam. The study is carried out by quantitative method through data from 408 subjects of different ages in Hanoi and Northern provinces. The findings of the study demonstrate that perceived usefulness, perceived ease of use, perceived enjoyment, and perceived privacy risk, have a significant impact on users' attitudes toward Virtual Try-On (VTO). Consequently, these factors increase their influence on customers' purchase intentions. Based on these results, the research group recommends that, in practical settings, enterprises concentrate on providing high-quality services, promoting their products to augment the aforementioned factors, and simultaneously addressing users' attitudes to enhance the overall customer experience. Therefore, this study provides valuable insights into the factors that influence customers' attitudes toward VTO technology, thereby contributing to the existing literature on the topic.Nghiên cứu chỉ ra những tác động của các nhân tố ảnh hưởng tới ý định mua hàng của người tiêu dùng qua hành vi sử dụng công nghệ trải nghiệm sản phẩm trực tuyến (Virtual Try-on - VTO) tại Việt Nam. Phương pháp định lượng được sử dụng để phân tích dữ liệu từ 408 đối tượng trong nhiều độ tuổi khác nhau trên địa bàn thành phố Hà Nội và các tỉnh thành phố miền Bắc. Kết quả cho thấy rằng các nhân tố như cảm nhận tính hữu ích, cảm nhận tính dễ sử dụng, cảm nhận tính thích thú, và cảm nhận rủi ro về quyền riêng tư có tác động đến thái độ của người dùng với công nghệ VTO từ đó gia tăng ảnh hưởng tới ý định mua sắm của khách hàng. Nhóm nghiên cứu đề xuất rằng, trong bối cảnh thực tiễn, doanh nghiệp cần tập trung vào cung cấp dịch vụ chất lượng, quảng bá sản phẩm để nâng cao các yếu tố đã được đề cập, đồng thời quan tâm đến thái độ của người dùng để cải thiện trải nghiệm tích cực cho khách hàng

A kinesin-based approach for inducing chromosome-specific mis-segregation in human cells

Various cancer types exhibit characteristic and recurrent aneuploidy patterns. The origins of these cancer type-specific karyotypes are still unknown, partly because introducing or eliminating specific chromosomes in human cells still poses a challenge. Here, we describe a novel strategy to induce mis-segregation of specific chromosomes in different human cell types. We employed Tet repressor or nuclease-dead Cas9 to link a microtubule minus-end-directed kinesin (Kinesin14VIb) from Physcomitrella patens to integrated Tet operon repeats and chromosome-specific endogenous repeats, respectively. By live- and fixed-cell imaging, we observed poleward movement of the targeted loci during (pro)metaphase. Kinesin14VIb-mediated pulling forces on the targeted chromosome were counteracted by forces from kinetochore-attached microtubules. This tug-of-war resulted in chromosome-specific segregation errors during anaphase and revealed that spindle forces can heavily stretch chromosomal arms. By single-cell whole-genome sequencing, we established that kinesin-induced targeted mis-segregations predominantly result in chromosomal arm aneuploidies after a single cell division. Our kinesin-based strategy opens the possibility to investigate the immediate cellular responses to specific aneuploidies in different cell types; an important step toward understanding how tissue-specific aneuploidy patterns evolve

A kinesin-based approach for inducing chromosome-specific mis-segregation in human cells

Various cancer types exhibit characteristic and recurrent aneuploidy patterns. The origins of these cancer type-specific karyotypes are still unknown, partly because introducing or eliminating specific chromosomes in human cells still poses a challenge. Here, we describe a novel strategy to induce mis-segregation of specific chromosomes in different human cell types. We employed Tet repressor or nuclease-dead Cas9 to link a microtubule minus-end-directed kinesin (Kinesin14VIb) from Physcomitrella patens to integrated Tet operon repeats and chromosome-specific endogenous repeats, respectively. By live- and fixed-cell imaging, we observed poleward movement of the targeted loci during (pro)metaphase. Kinesin14VIb-mediated pulling forces on the targeted chromosome were counteracted by forces from kinetochore-attached microtubules. This tug-of-war resulted in chromosome-specific segregation errors during anaphase and revealed that spindle forces can heavily stretch chromosomal arms. By single-cell whole-genome sequencing, we established that kinesin-induced targeted mis-segregations predominantly result in chromosomal arm aneuploidies after a single cell division. Our kinesin-based strategy opens the possibility to investigate the immediate cellular responses to specific aneuploidies in different cell types; an important step toward understanding how tissue-specific aneuploidy patterns evolve

Challenges and conceptual framework to develop heavy-load manipulators for smart factories

Industry 4.0 has been one of the emerging topics in recent years, covering a wide range of concepts and applications as well as political, economic and technological views. Manufacturing is becoming smarter and smarter at all levels, moving toward the concept of Smart Factory (SF), based on the advancements of digital transformation technologies, including Artificial Intelligence (AI) and bigdata analytics, and abilities to learn, configure and execute with cognitive intelligence of smart machines and automation systems. However, the SF adoption in practice, especially in Small and Medium-sized Enterprises (SMEs), is still in the early stage. In addition, there are growing demands of product personalisation, mass-customisation and diversification. Therefore, the involvement of humans is still importantly required in many production processes in SF models, where smart machines, smart manipulators, collaborative robots and Automated guided vehicles (AGVs) are required to co-work with humans, leading to an important concern of safety, reliability, productivity and quality of smart manufacturing systems. In this paper, challenges and a proposed conceptual framework to develop smart heavy-load manipulators are presented, with the focus on the cost-effectiveness and applicability in industrial practices of SF for SMEs

Validation and utilization of an internally controlled multiplex Real-time RT-PCR assay for simultaneous detection of enteroviruses and enterovirus A71 associated with hand foot and mouth disease

Background: Hand foot and mouth disease (HFMD) is a disease of public health importance across the Asia-Pacific region. The disease is caused by enteroviruses (EVs), in particular enterovirus A71 (EV-A71). In EV-A71-associated HFMD, the infection is sometimes associated with severe manifestations including neurological involvement and fatal outcome. The availability of a robust diagnostic assay to distinguish EV-A71 from other EVs is important for patient management and outbreak response. Methods: We developed and validated an internally controlled one-step single-tube real-time RT-PCR in terms of sensitivity, linearity, precision, and specificity for simultaneous detection of EVs and EV-A71. Subsequently, the assay was then applied on throat and rectal swabs sampled from 434 HFMD patients. Results: The assay was evaluated using both plasmid DNA and viral RNA and has shown to be reproducible with a maximum assay variation of 4.41 % and sensitive with a limit of detection less than 10 copies of target template per reaction, while cross-reactivity with other EV serotypes was not observed. When compared against a published VP1 nested RT-PCR using 112 diagnostic throat and rectal swabs from 112 children with a clinical diagnosis of HFMD during 2014, the multiplex assay had a higher sensitivity and 100 % concordance with sequencing results which showed EVs in 77/112 (68.8 %) and EV-A71 in 7/112 (6.3 %). When applied to clinical diagnostics for 322 children, the assay detected EVs in throat swabs of 257/322 (79.8 %) of which EV-A71 was detected in 36/322 (11.2 %) children. The detection rate increased to 93.5 % (301/322) and 13.4 % (43/322) for EVs and EV-A71, respectively, when rectal swabs from 65 throat-negative children were further analyzed. Conclusion: We have successfully developed and validated a sensitive internally controlled multiplex assay for rapid detection of EVs and EV-A71, which is useful for clinical management and outbreak control of HFMD. Keywords: Hand foot and mouth disease, Enteroviruses, Enterovirus A71, Real-time RT-PCR, Diagnosi