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1.
Stem Cells Transl Med ; 12(8): 553-568, 2023 08 16.
Article in English | MEDLINE | ID: mdl-37399126

ABSTRACT

Human embryonic stem cells-derived neural progenitor cells (hESCs-NPCs) transplantation holds great potential to treat stroke. We previously reported that delayed secondary degeneration occurs in the ventroposterior nucleus (VPN) of ipsilateral thalamus after distal branch of middle cerebral artery occlusion (dMCAO) in adult male Sprague-Dawley (SD) rats. In this study, we investigate whether hESCs-NPCs would benefit the neural recovery of the secondary damage in the VPN after focal cerebral infarction. Permanent dMCAO was performed with electrocoagulation. Rats were randomized into Sham, dMCAO groups with or without hESCs-NPCs treatment. HESCs-NPCs were engrafted into the peri-infarct regions of rats at 48 h after dMCAO. The transplanted hESCs-NPCs survive and partially differentiate into mature neurons after dMCAO. Notably, hESCs-NPCs transplantation attenuated secondary damage of ipsilateral VPN and improved neurological functions of rats after dMCAO. Moreover, hESCs-NPCs transplantation significantly enhanced the expression of BDNF and TrkB and their interaction in ipsilateral VPN after dMCAO, which was reversed by the knockdown of TrkB. Transplantated hESCs-NPCs reconstituted thalamocortical connection and promoted the formation of synapses in ipsilateral VPN post-dMCAO. These results suggest that hESCs-NPCs transplantation attenuates secondary damage of ipsilateral thalamus after cortical infarction, possibly through activating BDNF/TrkB pathway, enhancing thalamocortical projection, and promoting synaptic formation. It provides a promising therapeutic strategy for secondary degeneration in the ipsilateral thalamus post-dMCAO.


Subject(s)
Embryonic Stem Cells , Infarction, Middle Cerebral Artery , Neural Stem Cells , Humans , Embryonic Stem Cells/transplantation , Animals , Rats , Rats, Sprague-Dawley , Infarction, Middle Cerebral Artery/metabolism , Infarction, Middle Cerebral Artery/pathology , Infarction, Middle Cerebral Artery/therapy , Neural Stem Cells/transplantation , Cell Differentiation , Cell Movement , Signal Transduction , Neuroprotection , Thalamus/metabolism
2.
Brain Pathol ; 33(1): e13109, 2023 01.
Article in English | MEDLINE | ID: mdl-35794855

ABSTRACT

Epigenetic modification contributes to the pathogenesis of cerebral ischemia. Piwil2 belongs to the PIWI proteins subfamily and has a key role in the regulation of gene transcription through epigenetics. However, the roles of Piwil2 in cerebral ischemia have not been investigated. In this study, we aim to elucidate the roles and the underlying molecular mechanisms of Piwil2 in ischemic tolerance induced by hypoxic postconditioning (HPC) against transient global cerebral ischemia (tGCI). We found that the expression of Piwil2 in CA1 was downregulated by HPC after tGCI. Silencing Piwil2 with antisense oligodeoxynucleotide (AS-ODN) in CA1 after tGCI decreased the expression of apoptosis-related proteins and exerted neuroprotective effects. Opposite results were observed after overexpression of Piwil2 induced by administration of Piwil2-carried lentivirus. Furthermore, we revealed differentially expressed Piwil2-interacting piRNAs in CA1 between HPC and tGCI groups by RNA binding protein immunoprecipitation (RIP) assay. Moreover, downregulating Piwil2 induced by HPC or AS-ODN after tGCI caused a marked reduction of DNA methyltransferase 3A (DNMT3A), which in turn abolished the tGCI-induced increase in the DNA methylation of cyclic AMP response element-binding 2 (CREB2), thus increasing mRNA and protein of CREB2. Finally, downregulating Piwil2 restored dendritic complexity and length, prevented the loss of dentritic spines, thereby improving cognitive function after tGCI. These data firstly reveal that Piwil2 plays an important part in HPC-mediated neuroprotection against cerebral ischemia through epigenetic regulation of CREB2.


Subject(s)
Brain Ischemia , Ischemic Attack, Transient , Animals , Rats , Brain Ischemia/pathology , CA1 Region, Hippocampal/pathology , Cerebral Infarction/pathology , Epigenesis, Genetic , Ischemic Attack, Transient/metabolism , Ischemic Attack, Transient/pathology , Ischemic Attack, Transient/prevention & control , Methylation , Rats, Wistar , RNA-Binding Proteins/metabolism
3.
Sensors (Basel) ; 22(14)2022 Jul 18.
Article in English | MEDLINE | ID: mdl-35891023

ABSTRACT

Scholte waves at the seafloor have significant potential for underwater detection and communication, so a study about detecting Scholte waves is very meaningful in practice. In this paper, the detection of Scholte waves at the seafloor is researched theoretically and experimentally. Acoustic models with the multilayer elastic bottom are established according to the ocean environment, and a tank experiment is designed and carried out to detect Scholte waves. Different from detecting Scholte waves in the seismic wavefield, a technique for detecting Scholte waves in the sound pressure field is proposed in this paper. The experimental results show that the proposed technique can detect Scholte waves effectively, and there are no problems such as seabed coupling and the effect of wave speeds. Furthermore, the results also show that this detection technique is still effective in conditions with a sediment layer. The existence of sediment layers changes the acoustic field conditions and affects the excitation of Scholte waves.


Subject(s)
Acoustics , Sound
4.
ACS Appl Mater Interfaces ; 14(1): 2202-2210, 2022 Jan 12.
Article in English | MEDLINE | ID: mdl-34978403

ABSTRACT

Collecting water from fog flow is emerging as a promising solution to the water shortage problem. This work demonstrated a novel environmentally responsive water collector made from a self-prepared Janus polyvinyl alcohol sponge in combination with a two-way shape memory alloy spring, which transforms the traditional manner of static water collection into a dynamic one. The unidirectional water transport of the Janus structure together with the dynamic collection approach correspond to a 30.8% increase in the water-collection rate (WCR). The resultant WCR is up to 5.1 g/h, which ranks relatively high compared to similar studies. The light- and thermal-response capability, easy fabrication, and good cycling performance indicate that our devices could be utilized in a variety of applications. In this work, an efficient, intelligent adaptive, simple-preparation, precision-guided, and economical fog-collecting devices are recommended. Our work provides new insights on the design of high-efficient water collectors with practicability.

5.
Antioxid Redox Signal ; 36(7-9): 567-591, 2022 03.
Article in English | MEDLINE | ID: mdl-34714119

ABSTRACT

Aims: Rhodiola sacra is a widely used pharmaceutical component with multiple functions, including anti-oxidation and anti-inflammation. However, the exact mechanisms involved in neuroprotection against transient global cerebral ischemia (tGCI) remain to be elucidated. Herein, we aim at closing the gap in understanding on whether rhodiola sacra reduces neuronal death in hippocampal CA1 and at demonstrating how rhodiola sacra offers neuroprotection after tGCI. Results: The results show that rhodiola sacra (2.4 g/kg/d by feeding) pretreatment or/and postreatment significantly alleviated neuronal injury, inhibited glial activation, and improved cognitive function in male rats subjected to tGCI. The neuroprotection of prophylaxis with rhodiola sacra is equivalent to that of therapeutics. The binding mode of adenosine monophosphate-activated protein kinase (AMPK) α2-subunit with rhodiola sacra was predicted by molecular docking. Further, rhodiola sacra upregulates phosphorylated AMPK and promotes nuclear translocation of nuclear factor erythroid 2 related factor 2 (Nrf2). In addition, rhodiola sacra increases heme oxygenase-1 (HO-1) expression and activity and reduces malondialdehyde (MDA) content in CA1 after tGCI. However, the neuroprotection of rhodiola sacra is abolished by Nrf2 knockdown with small interfering RNA (siRNA) after tGCI. Similarly, the inhibition of AMPK with Compound C or siRNA against AMPK α2 aggravates neuronal death after tGCI through decreasing nuclear Nrf2 and the expression and activity of HO-1, and by increasing the release of MDA. Innovation and Conclusion: For the first time, this study demonstrates that as a prophylactic or therapeutic agent rhodiola sacra prevents oxidant stress, protects neurons, and improves cognitive function through activating the AMPK/Nrf2 pathway in tGCI rats. Antioxid. Redox Signal. 36, 567-591.


Subject(s)
Brain Ischemia , Ischemic Attack, Transient , Neuroprotective Agents , Rhodiola , AMP-Activated Protein Kinases/metabolism , Animals , Brain Ischemia/drug therapy , Brain Ischemia/metabolism , CA1 Region, Hippocampal/metabolism , Ischemic Attack, Transient/metabolism , Male , Molecular Docking Simulation , NF-E2-Related Factor 2/metabolism , Neuroprotective Agents/metabolism , Neuroprotective Agents/pharmacology , Neuroprotective Agents/therapeutic use , Rats , Rats, Wistar , Rhodiola/metabolism , Sacrum/metabolism
6.
RSC Adv ; 11(24): 14769-14776, 2021 Apr 15.
Article in English | MEDLINE | ID: mdl-35424002

ABSTRACT

Collecting water from fog flow has emerged as a promising strategy for the relief of water shortage problems. Herein, using a UV-induced (ultraviolet light induced) controllable diffusion method combined with technology of three-dimensional (3D) printing, we fabricate biomimetic materials incorporating beetle-like hydrophobic-hydrophilic character and cactus-like cone arrays with various structure parameters, and then systematically study their fog-harvesting performance. The UV-induced controllable diffusion method can break away from the photomask to regulate the hybrid wettability. Moreover, employing 3D printing technology can flexibly control the structure parameters to improve the water collection efficiency. It is found that the water collection rate (WCR) can be optimized by controlling the hybrid wettability of the sample surface and cone distance and using substrates with printed holes, which lead to a 109% increase of WCR.

7.
J Acoust Soc Am ; 134(1): 166-75, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23862795

ABSTRACT

A tank experiment and theoretical analysis are carried out to study acoustic Bragg scattering by a sinusoidal surface with period 0.3 m and amplitude 2 cm between water and sand sediment. The penetrating field is measured in the frequency range from 20 to 40 kHz at grazing angles 10° to 90° in the tank. A theoretical solution for acoustic scattering by the sinusoidal surface is derived to explain the interference pattern observed in the experiment. The result shows that the minus first order Bragg scattering wave is strong enough to interfere with the refracted wave obeying Snell's law, forming interference patterns that can be detected experimentally.

8.
J Acoust Soc Am ; 131(1): 47-53, 2012 Jan.
Article in English | MEDLINE | ID: mdl-22280570

ABSTRACT

A generalized model is applied to estimate the incoherent penetration ratio caused by volume scattering at grazing angles below the critical grazing angle. The factors that affect volume scattering have been discussed using experimental data in literature. A two-layered model that refers to sound scattering in two-layered media is used to evaluate the incoherent penetration ratio for most typical sediments. But for special cases, such as the experiment, SAX04, a three-layered model is necessary to describe scattering features especially for grazing angles θ<30°. It is shown that subcritical penetration is enhanced when the scale of volume fluctuations is comparable with the acoustic wavelength, and the scattered waves into the seafloor dominate over evanescent waves at depths larger than a few wavelengths.

9.
Clin Cancer Res ; 12(21): 6523-31, 2006 Nov 01.
Article in English | MEDLINE | ID: mdl-17085667

ABSTRACT

PURPOSE: A dual-regulated adenovirus variant CNHK500, in which human telomerase reverse transcriptase promoter drove the adenovirus 5 (Ad5) E1a gene and hypoxia-response promoter controlled the E1b gene, was engineered. This virus has broad anticancer spectrum and higher specificity compared with mono-regulated adenovirus CNHK300. The objective of the current study is to show its antitumor selectivity and therapeutic potential. EXPERIMENTAL DESIGN: The antitumor specificity of human telomerase reverse transcriptase and hypoxia response promoters was evaluated in a panel of tumor and normal cells. Under the control of these promoters, the tumor-selective expression of E1a and E1b genes was evaluated. Further in vitro antitumor specificity and potency of this virus were characterized by viral replication and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. Subsequently, hepatocellular carcinoma xenografts were established to evaluate CNHK500 antitumor efficacy in vivo by different routes of virus administration and different dosages. RESULTS: Human telomerase reverse transcriptase and hypoxia response promoters were activated in a tumor-selective manner or under hypoxia treatment in a broad panel of cells. Selective adenoviral early gene expression, efficient viral replication, and oncolysis were observed in all tested cancer cells with more attenuated replication capacity in normal cells. Significant regression of hepatocellular carcinoma xenografts and prolonged survival were observed by either i.t. or i.v. administration. CONCLUSIONS: CNHK500 greatly reduced side effects in normal cells via dual control of adenoviral essential genes while still preserving potent antitumor efficacy on broad-spectrum cancer cells in vitro and in vivo. It can be used as a powerful therapeutic agent not only for liver cancers but also for other solid tumors.


Subject(s)
Carcinoma, Hepatocellular/therapy , Cell Hypoxia/genetics , Liver Neoplasms/therapy , Neoplasms, Experimental/therapy , Oncolytic Virotherapy/methods , Oncolytic Viruses/genetics , Adenoviridae/genetics , Adenovirus E1A Proteins/biosynthesis , Adenovirus E1A Proteins/genetics , Adenovirus E1B Proteins/biosynthesis , Adenovirus E1B Proteins/genetics , Animals , Blotting, Western , Carcinoma, Hepatocellular/virology , Cell Line, Tumor , DNA Primers , Gene Expression , Humans , Liver Neoplasms/virology , Mice , Mice, Nude , Neoplasms, Experimental/virology , Promoter Regions, Genetic , Telomerase/genetics , Transcription, Genetic , Xenograft Model Antitumor Assays
10.
Mol Ther ; 13(5): 918-27, 2006 May.
Article in English | MEDLINE | ID: mdl-16497559

ABSTRACT

Among numerous gene therapeutic strategies for cancer treatment, gene transfer by conditionally replicative adenovirus (CRAd) of interferon-gamma (IFN-gamma) may be useful because of the possibility that it will yield IFN-gamma-mediated antiangiogenesis, immune responses, and CRAd-mediated oncolysis. In this study, we constructed a human TERT promoter-mediated oncolytic adenovirus targeting telomerase-positive cancers and armed with a mouse or human IFN-gamma gene to generate novel immune gene-viral therapeutic systems, CNHK300-mIFN-gamma and CNHK300-hIFN-gamma, respectively. The systems can specifically target, replicate in, and lyse cancer cells, while sparing normal cells. The advantage of these systems is that the number of transgene copies and their expression increase markedly via viral replication within infected cancer cells, and replicated viral progeny can then infect additional cancer cells within the tumor mass. CNHK300-mIFN-gamma induced regression of xenografts in liver cancer models in both immunodeficient and immunocompetent mice by triplex mechanisms including selective oncolysis, antiangiogenesis, and immune responses. We conclude that combining immune gene therapy and oncolytic virotherapy can enhance antitumor efficacy as a result of synergism between CRAd oncolysis and transgene composite antitumor responses.


Subject(s)
Adenoviridae/genetics , Genetic Therapy , Interferon-gamma/genetics , Interferon-gamma/therapeutic use , Liver Neoplasms, Experimental/therapy , Adenoviridae/physiology , Adenovirus E1A Proteins/genetics , Animals , Cell Line , Cell Line, Tumor , DNA-Binding Proteins/genetics , Genetic Vectors/administration & dosage , Genetic Vectors/therapeutic use , Humans , Liver Neoplasms, Experimental/pathology , Mice , Mice, Inbred BALB C , Mice, Nude , Neoplasm Transplantation , Neovascularization, Pathologic/prevention & control , Telomerase/genetics , Transgenes , Transplantation, Heterologous , Virus Replication
11.
Hepatobiliary Pancreat Dis Int ; 2(4): 581-6, 2003 Nov.
Article in English | MEDLINE | ID: mdl-14627524

ABSTRACT

OBJECTIVE: To explore the prognostic factors of gallbladder carcinoma and the relationship between operative procedure and prognosis of gallbladder carcinoma. METHOD: A retrospective clinical analysis was made in 56 patients with gallbladder carcinoma who had undergone surgery at our department from 1995 to 2001. RESULTS: Of the 56 patients, 20 were men and 36 women with a male to female ratio of 1:1.56. Their age ranged from 41 to 79 years with a mean of 59.6 years. Thirty-four patients suffered from gallstones. Abdominal pain (83.9%) and jaundice (41.1%) were the main symptoms. Thirty patients (Nevin stage II in 5 patients, III in 3, IV in 4, and V in 18) received radical or extended radical resection; non-radical resection was performed in 11 patients of Nevin stage V; and 15 patients of Nevin stage V were subjected to biopsy with or without palliative bypass procedure. Statistical analysis showed that operative procedure, staging of Nevin, and gallstone affected significantly postoperative survival, but age, sex, preoperative serum bilirubin level, numbers of tumor location, histopathological type and grade were not significant prognostic factors. After radical resection was classified with Nevin staging, we found that all the patients of stage II were alive. Meanwhile the postoperative survival periods of radical resection groups of stage III to V, palliative resection group, and biopsy with/without palliative drainage group were statistically different. CONCLUSIONS: From Nevin stage II to V, the survival period of respective stage group, which treated with curative operation, became shorter gradually. In those patients of stage V, the survival period of curative operation group was longer than that of palliative resection group, and that of the latter was better than that of biopsy with/without palliative drainage group. So radical resection was still the unique way to better prognosis.


Subject(s)
Carcinoma/mortality , Carcinoma/surgery , Cholecystectomy/methods , Gallbladder Neoplasms/mortality , Gallbladder Neoplasms/surgery , Adult , Age Distribution , Aged , Biopsy, Needle , Carcinoma/secondary , Cholangiopancreatography, Endoscopic Retrograde , Cholecystectomy/mortality , Female , Gallbladder Neoplasms/pathology , Humans , Lymph Node Excision/methods , Lymphatic Metastasis , Male , Middle Aged , Neoplasm Staging , Probability , Prognosis , Proportional Hazards Models , Retrospective Studies , Risk Assessment , Sampling Studies , Sex Distribution , Survival Analysis , Tomography, X-Ray Computed , Treatment Outcome
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