RESUMO
Ionogels possess high conductivity, stretchability, and adhesion, making them promising as flexible sensors. However, it remains challenging to fabricate an ionogel which integrates excellent environment endurance, superior mechanical strength, high self-healing efficiency, and super adhesion. Herein, a supramolecular ionic liquid is synthesized using calcium chloride and 1-butyl-3-methylimidazolium chloride. An advanced ionogel based on this supramolecular ionic liquid is conveniently constructed by a one-pot method with acrylamide and acrylic acid as monomers. The supramolecular cross-linking network, formed by affluent coordination interactions, hydrogen bonds, and electrostatic interactions, provides the ionogel with ideal mechanical strength (tensile strength up to 1.7 MPa), high self-healing efficiency (up to 149%), super adhesion (up to 358 kPa on aluminum), excellent solvent tolerance (less than 10% weight increase, high mechanical and sensing performance retention after being soaked in organic solvents), and low-temperature endurance (breaking elongation can reach 87% at -30 °C). The supramolecular ionogels can function as multi-mode sensors, capable of monitoring strain and different amplitudes of human movements in real-time. Moreover, the sensing performance of ionogels remains unaffected even after being self-healed or exposure to organic solvents. It is expected that this study could offer valuable design ideas to construct advanced gel materials applicable in complicated environment.
Assuntos
Líquidos Iônicos , Humanos , Acrilamida , Temperatura Baixa , Condutividade Elétrica , Ligação de HidrogênioRESUMO
Cellular energy metabolism dysregulation is associated with colorectal cancer (CRC) development and progression. Discoidin domain receptor 1a (DDR1a), one of the five DDR1 isoforms, is closely related to cell proliferation, invasion, and apoptosis in various tumors. Whether it participates in cellular metabolic reprogramming and regulates CRC initiation and progression remains unclear. In this study, we compared the expression of DDR1 in CRC tissues and adjacent tissues from 126 postoperative CRC samples. Moreover, lentivirus-mediated DDR1a overexpression and knockdown were performed in LoVo cells, and cell viability and proliferation were determined by CCK-8 and BrdU assays, respectively. Oxygen consumption rate, extracellular acidification rate, and lactate production were used to determine the effect of DDR1a on metabolic reprogramming. Clinically, CRC patients with high DDR1 expression had poor differentiation and were at an advanced TNM stage. DDR1a promoted LoVo cell proliferation, mitochondrial function, and extracellular acidification. Moreover, DDR1a knockdown inhibited intracellular lactic acid production in LoVo cells, while a pyruvate kinase inhibitor (diamide, 200â µM) significantly reversed this progression. Taken together, our results reveal that DDR1 plays a crucial role in maintaining intracellular environment homeostasis through metabolic reprogramming.
Assuntos
Proliferação de Células , Neoplasias Colorretais , Receptor com Domínio Discoidina 1 , Metabolismo Energético , Humanos , Bromodesoxiuridina/metabolismo , Linhagem Celular Tumoral , Movimento Celular/fisiologia , Proliferação de Células/genética , Neoplasias Colorretais/genética , Neoplasias Colorretais/metabolismo , Diamida , Receptor com Domínio Discoidina 1/genética , Receptor com Domínio Discoidina 1/metabolismo , Receptores com Domínio Discoidina/metabolismo , Metabolismo Energético/genética , Ácido Láctico , Isoformas de Proteínas/metabolismo , Piruvato Quinase/metabolismo , Receptores Proteína Tirosina Quinases/metabolismo , Sincalida/metabolismoRESUMO
5-Fluorouracil (5-FU) is a common chemotherapy drug for patients with advanced colorectal cancer; however, many patients develop resistance to 5-FU and suffer from treatment failure. Discoidin domain receptor 1 (DDR1) is upregulated in multiple cancers and positively associated with chemoresistance. We explored the effect of DDR1a on the cytotoxicity induced by 5-FU in LoVo cells and the underlying mechanism. Therefore, DDR1a overexpression (DDR1ahigh) and knockdown in LoVo cell lines (shDDR1a) were constructed to detect cell viability and cytotoxicity induced by 5-FU. The results showed that cell viability of DDR1ahigh cells was higher in comparison with that of the control group. When 5-FU (5 µM) was administered, the percentage of apoptotic cells, cytochrome C release and caspase-3 activity was found to be higher in the shDDR1a group than that in the control group. Both of PI3K and MDM2 proteins level decreased in DDR1ahigh and shDDR1a, but the BAX/Bcl-2 level in the shDDR1a group increased compared to that in the control. Therefore, DDR1a might be a potential therapeutic target for 5-FU chemoresistance in colorectal cancer.
