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Microfluidics is now extensively used for cellular analysis due to its merits of sensitivity, accuracy, and miniaturization. The push-pull probe is built on microfluidic principles but innovatively uses hydrodynamic forces instead of closed microchannels for liquid confinement. Although various microfluidic probes have been developed for cell manipulation and analysis, few have addressed the integration and optical challenges posed by vertically oriented probes, which are difficult to accommodate in compact experimental setups and often interfere with optical imaging pathways. In this work, we present an inclined push-pull (IPP) microfluidic probe designed with a 45° angle for precise cell staining and calcium channel activation in situ. Compared with conventional vertical push-pull probes, the inclined design not only enabled in situ cell manipulation with high-resolution bright-field imaging but also freed up vertical space for operations and device integration. The results indicated that the proposed IPP probe could provide an alternative tool for in situ cell manipulation and analysis, and it is expected to enable broader applications in research including cellular regulation, drug discovery, and efficacy assessment.
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http://dx.doi.org/10.1021/acs.analchem.5c02265 | DOI Listing |
Methods Cell Biol
September 2025
LR18ES03 Laboratory of Neurophysiology, Cellular Physiopathology and Valorisation of Biomolecules, Faculty of Science of Tunis, University Tunis El Manar, Tunis, Tunisia. Electronic address:
Breast cancer (BC) represents a major socio-economic challenge worldwide due to its high morbidity and mortality rates. Despite various therapeutic strategies, the heterogeneity of breast cancer and the resistance of tumour cells often lead to treatment failure. Consequently, the use of animal models of BC is crucial for understanding the cellular and molecular mechanisms involved in the different stages of carcinogenesis and for screening new drugs to assess their efficacy, potential safety and side effects.
View Article and Find Full Text PDFJ Thorac Cardiovasc Surg
September 2025
Department of Cardiovascular Surgery, Kanazawa University, Takaramachi 13-1 Kanazawa 920-8641, Japan.
Objective: To assess the production of nitric oxide and endothelin in off-pump coronary artery bypass grafting by comparing two techniques of internal thoracic artery preparation: skeletonized and pedicled without endothoracic fascia.
Methods: In this prospective, randomized clinical study, 40 patients undergoing off-pump coronary artery bypass grafting were randomized according to internal thoracic artery preparation technique into the skeletonized or pedicled (without endothoracic fascia) groups (n=20 each). Endothelial expression of CD31 was evaluated by means of immunohistochemistry and en-face immunofluorescence.
J Hazard Mater
September 2025
School of Ecology and Environment, Zhengzhou University, Zhengzhou 450001, China; Henan Key Laboratory of Environmental Chemistry and Low Carbon Technology, Zhengzhou 450001, China. Electronic address:
Solid electrolyte cell is a novel gas purification approach, which has unique superiority in simultaneous nitrogen oxides (NO) and volatile organic compounds (VOCs) removal. The development of effective electrode materials and the comprehensive understanding of reaction mechanisms are essential to advancing this technology. In this study, LaPrBaNiO (x = 0, 0.
View Article and Find Full Text PDFPathol Res Pract
September 2025
Department of Pathology, Xijing Hospital and School of Basic Medicine, Fourth Military Medical University, Xi'an, China. Electronic address:
Background: Dermal clear cell sarcoma (DCCS) is a rare malignant mesenchymal neoplasm. Owing to the overlaps in its morphological and immunophenotypic profiles with a broad spectrum of tumors exhibiting melanocytic differentiation, it is frequently misdiagnosed as other tumor entities in clinical practice. By systematically analyzing the clinicopathological characteristics, immunophenotypic features, and molecular biological properties of DCCS, this study intends to further enhance pathologists' understanding of this disease and provide a valuable reference for its accurate diagnosis.
View Article and Find Full Text PDFPLoS Comput Biol
September 2025
Department of Genome Sciences, University of Washington, Seattle, Washington, United States of America.
Fanconi Anemia (FA) is a heritable syndrome characterized by DNA damage repair deficits, frequent malformations and a significantly elevated risk of bone marrow failure, leukemia, and mucosal head and neck squamous cell carcinomas (HNSCC). Hematopoietic stem cell gene therapy can prevent marrow failure and lower leukemia risk, but mucosal gene therapy to lower HNSCC risk remains untested. Major knowledge gaps include an incomplete understanding of how rapidly gene-corrected cellular lineages could spread through the oral epithelium, and which delivery parameters are critical for ensuring efficient gene correction.
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