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In this Letter, a quasi-distributed quartz enhanced photoacoustic spectroscopy (QEPAS) gas sensing system based on hollow waveguide micropores (HWGMP) was reported for the first time, to the best of our knowledge. Three micropores were developed on the HWG to achieve distributed detection units. Three self-designed quartz tuning forks (QTFs) with low resonant frequency of 8.7â kHz were selected as the acoustic wave transducer to improve the detection performance. Compared with micro-nano fiber evanescent wave (FEW) QEPAS, the HWGMP-QEPAS sensor has advantages such as strong anti-interference ability, low loss, and low cost. Acetylene (C2H2) was selected as the target gas to verify the characteristics of the reported sensor. The experimental results showed that the three QTFs almost had the same sensing ability and possessed an excellent linear concentration response to C2H2. The minimum detection limits (MDLs) for the three QTFs were determined as 68.90, 68.31, and 66.62â ppm, respectively. Allan deviation analysis indicated that the system had good long-term stability, and the MDL can be improved below 3â ppm in an average time of 1000â s.
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The Fresnel reflection of a splice from the air-silica interface between a hollow-core fiber (HCF) and a solid-core conventional fiber will increase the splicing loss and also cause possible instability of transmission. Here, for the first time, we develop a novel approach to fusion splicing an antireflection-coated (AR-coated) conventional fiber and an antiresonant HCF, which was generally claimed to be impossible because of the heat-induced damage of the coating, and achieve state-of-the-art ultralow fusion splicing loss less than 0.3â dB and a low return loss less than -28â dB by optimizing the splicing procedures and parameters. Our new fusion splicing approach will benefit the wide application of HCFs in telecoms, laser technologies, gyroscopes, and fiber gas cells.
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The nanobore fiber (NBF) is a promising nanoscale optofluidic platform due to its long nanochannel and unique optical properties. However, so far, the applications of NBF have been based only on its original fiber geometry without any extra functionalities, in contrast with various telecom fiber devices, which may limit its wide applications. Here, we provide the first, to the best of our knowledge, demonstration of NBF-based fiber Bragg gratings (FBGs) introduced by either the femtosecond (fs) laser direct writing technique or the ultraviolet (UV) laser phase mask technique. Moreover, the FBG fabricated via the UV laser was optimized, achieving a high reflectivity of 96.89% and simultaneously preserving the open nanochannel. The NBF-based FBGs were characterized in terms of temperature variation and the infiltration of different liquids, and they showed high potential for nanofluidic applications.
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Gliomas are the most common primary intracranial tumor, accounting for more than 70% of brain malignancies. Studies indicate that highly upregulated in liver cancer (HULC), a long noncoding RNA (lncRNA), functions as an oncogene in gliomas. However, the underlying mechanism of HULC in gliomas remains under-studied and was subsequently investigated in the current study. Brain tissues were clinically collected from 50 patients with glioblastoma (GBM) and 35 patients with acute craniocerebral injury, followed by immunohistochemical detection of the expression patterns of Forkhead box M1 (FOXM1), anterior gradient 2 (AGR2), and hypoxia-inducible factor-1α (HIF-1α). After flow cytometry-based sorting of the CD133+ glioma stem cells (GSCs) from the U251 cell line, the obtained cells were subjected to lentivirus infection. Afterwards, the proliferation, stemness, and apoptosis of GSCs were evaluated using sphere formation, immunofluorescence, and flow cytometry assays, respectively. In addition, the interactions among HULC, FOXM1, AGR2, and HIF-1α were identified using RNA immunoprecipitation (RIP), RNA pull-down, Chromatin immunoprecipitation (ChIP), IP, and dual luciferase reporter assays. Last, the specific effects were validated in vivo. HULC was upregulated in GBM tissues and GSCs, which may promote the progression of glioma. On the other hand, silencing of HULC reduced the stemness, inhibited the proliferation, and promoted the apoptosis and differentiation of GSCs. In addition, HULC further stabilized FOXM1 expression in GSCs through ubiquitination, while FOXM1 activated AGR2 transcription to promote HIF-1α expression. Moreover, HULC promoted the glycolysis and stemness of GSCs through its regulation of the FOXM1/AGR2/HIF-1α axis, consequently exacerbating the occurrence and development of glioma. The findings obtained in our study indicate that HULC stabilizes the FOXM1 protein by ubiquitination to upregulate the expression of AGR2 and HIF-1α, which further promote the glycolysis of and maintain the stemness of GSCs, to enhance the tumorigenicity of GSCs, highlighting a novel therapeutic target for glioma.
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Neoplasias Encefálicas , Glioblastoma , Glioma , Células-Tronco Neoplásicas , RNA Longo não Codificante , Neoplasias Encefálicas/genética , Linhagem Celular Tumoral , Proliferação de Células/genética , Proteína Forkhead Box M1/genética , Proteína Forkhead Box M1/metabolismo , Regulação Neoplásica da Expressão Gênica , Glioblastoma/genética , Glioma/genética , Glicólise , Humanos , Subunidade alfa do Fator 1 Induzível por Hipóxia/genética , Subunidade alfa do Fator 1 Induzível por Hipóxia/metabolismo , Mucoproteínas/genética , Mucoproteínas/metabolismo , Proteínas Oncogênicas/genética , Proteínas Oncogênicas/metabolismo , RNA Longo não Codificante/genéticaRESUMO
Hybrid optical fibers have been widely investigated in different architectures to build integrated fiber photonic devices and achieve various applications. Here we proposed and fabricated hybrid microfiber waveguides with self-growing polymer nanofilms on the surfaces of microfibers triggered by evanescent field of light for the first time. We have demonstrated the polymer nanofilm of â¼50â nm can be grown on the microfiber with length up to 15â mm. In addition, the roughness of nanofilm can be optimized by controlling the triggering laser power and exposure duration, and the total transmission loss of the fabricated hybrid microfiber is less than 2â dB within a wide wavelength range. The hybrid polymer nanofilm microfiber waveguides have been characterized and their relative humidity (RH) responses have also been tested, indicating a potential for RH sensing. Our fabrication method may also be extended to construct the hybrid microfibers with different functional photopolymer materials.
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Optofluidic microlenses are one of the crucial components in many miniature lab-on-chip systems. However, many optofluidic microlenses are fabricated through complex micromachining and tuned by high-precision actuators. We propose a kind of tunable optofluidic microbubble lens that is made by the fuse-and-blow method with a fiber fusion splicer. The optical focusing properties of the microlens can be tuned by changing the refractive index of the liquid inside. The focal spot size is 2.8 µm and the focal length is 13.7 µm, which are better than those of other tunable optofluidic microlenses. The imaging capability of the optofluidic microbubble lens is demonstrated under a resolution test target and the imaging resolution can reach 1 µm. The results indicate that the optofluidic microbubble lens possesses good focusing properties and imaging capability for many applications, such as cell counting, optical trapping, spatial light coupling, beam shaping and imaging.
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Lentes , Técnicas Analíticas Microfluídicas , Contagem de Células , Microbolhas , RefratometriaRESUMO
Ventriculoatrial shunts are the most common second-line procedure for cases in which ventriculoperitoneal shunts are unsuitable. Shunting-associated thrombosis is a potentially life-threatening complication after ventriculoatrial shunt insertion. The overall prevalence of this complication is still controversial because of substantial differences in the numbers found in studies using clinical data and in those analyzing postmortem findings. The etiology of thrombosis may be multifactorial, including shunt catheter itself, contents of cerebrospinal fluid, shunt infection, and genetic disorder. The clinical presentation can vary widely, ranging from asymptomatic to a life-threatening condition. Timely recognition of thromboembolic lesions is critical for treatment. However, early diagnosis and management is still challenging because of a relatively long asymptomatic latency and lack of clear guideline recommendations. The purpose of this review is to provide an overview of ventriculoatrial shunt thrombosis, especially to focus on its etiopathogenesis, diagnosis, treatment, and prevention.
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Hidrocefalia , Tromboembolia , Trombose , Derivações do Líquido Cefalorraquidiano/efeitos adversos , Humanos , Hidrocefalia/complicações , Hidrocefalia/cirurgia , Trombose/etiologia , Derivação Ventriculoperitoneal/efeitos adversos , Derivação Ventriculoperitoneal/métodosRESUMO
Accumulating evidences have suggested that extracellular vesicles (EVs) are crucial players in the pathogenesis of ischemic brain injury. This study was designed to explore the specific functions of M2 phenotype microglia-derived EVs in ischemic brain injury progression. The expression of microRNA-135a-5p (miR-135a-5p) in M2 microglia-derived EVs was determined by reverse transcription-quantitative polymerase chain reaction (RT-qPCR), followed by the identification of expression relationship among miR-135a-5p, thioredoxin-interacting protein (TXNIP), and nod-like receptor protein 3 (NLRP3) by dual luciferase reporter gene assay. After construction of an oxygen-glucose deprivation/reperfusion (OGD/R) cell model, the effects of miR-135a-5p on the biological characteristics of HT-22 cells were assessed by cell counting kit 8 (CCK-8) assay and flow cytometry. Finally, a mouse model of transient middle cerebral artery occlusion (tMCAO) was established and cerebral infarction volume was determined by triphenyltetrazolium chloride (TTC) staining and the expression of IL-18 and IL-1ß in the brain tissue was determined by enzyme-linked immunosorbent assay (ELISA). We found that M2 microglia-derived EVs had high expression of miR-135a-5p, and that miR-135a-5p in M2 microglia-derived EVs negatively regulated the expression of NLRP3 via TXNIP. Overexpression of miR-135a-5p promoted the proliferation but inhibited the apoptosis of neuronal cells, and inhibited the expression of autophagy-related proteins. M2 microglia-derived EVs delivered miR-135a-5p into neuronal cells to inhibit TXNIP expression, which further inhibited the activation of NLRP3 inflammasome, thereby reducing neuronal autophagy and ischemic brain injury. Hence, M2 microglia-derived EVs are novel therapeutic targets for ischemic brain injury treatment.
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Isquemia Encefálica/metabolismo , Proteínas de Transporte/metabolismo , Vesículas Extracelulares , MicroRNAs/metabolismo , Microglia/química , Proteína 3 que Contém Domínio de Pirina da Família NLR/metabolismo , Tiorredoxinas/metabolismo , Animais , Proteínas de Transporte/genética , Vesículas Extracelulares/química , Vesículas Extracelulares/metabolismo , Masculino , Camundongos , Camundongos Endogâmicos ICR , MicroRNAs/genética , Proteína 3 que Contém Domínio de Pirina da Família NLR/genética , Tiorredoxinas/genéticaRESUMO
Negative curvature hollow-core fibers (NC-HCFs) can boost the excellent performance of HCFs in terms of propagation loss, nonlinearity, and latency, while retaining large core and delicate cladding structures, which makes them distinctly different from conventional fibers. Construction of low-loss all-fiber NC-HCF architecture with conventional single-mode fibers (SMFs) is important for various applications. Here we demonstrate an efficient and reliable fusion splicing method to achieve low-loss connection between a NC-HCF and a conventional SMF. By controlling the mode-field profile of the SMF with a two-step reverse-tapering method, we realize a record-low insertion loss of 0.88 dB for a SMF/NC-HCF/SMF chain at 1310 nm. Our method is simple, effective, and reliable, compared with those methods that rely on intermediate bridging elements, such as graded-index fibers, and can greatly facilitate the integration of NC-HCFs and promote more advanced applications with such fibers.
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Microstructured optical fibers (MOFs) have attracted intensive research interest in fiber-based optofluidics owing to their ability to have high-efficient light-microfluid interactions over a long distance. However, there lacks an exquisite design guidance for the utilization of MOFs in subwavelength-scale optofluidics. Here we propose a tapered hollow-core MOF structure with both light and fluid confined inside the central hole and investigate its optofluidic guiding properties by varying the diameter using the full vector finite element method. The basic optical modal properties, the effective sensitivity, and the nonlinearity characteristics are studied. Our miniature optofluidic waveguide achieves a maximum fraction of power inside the core at 99.7%, an ultra-small effective mode area of 0.38 µm2, an ultra-low confinement loss, and a controllable group velocity dispersion. It can serve as a promising platform in the subwavelength-scale optical devices for optical sensing and nonlinear optics.
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Multicore fibers (MCFs) offer a fascinating solution to the need to increase the fiber density and thus meet the exponentially growing demand for capacity in optical communication networks. Despite overwhelming research into MCFs, the desire for a general fusion splicing scheme between dissimilar MCFs remains unanswered. Here, we propose a tapering technique to reshape MCFs that includes both reverse-tapering and down-tapering schemes and can be exploited to tailor the core-to-core spacing and modify the modal property of MCFs. By matching both the spacing and the mode field diameter, we demonstrated a low-loss (0.18 ± 0.10â dB) and low-crosstalk (-68 ± 3â dB) fusion splice between two spacing-mismatched MCFs with a spacing difference of up to 26â µm. The proposed novel schemes are also suitable for splicing between MCFs with slightly different spacings and can provide a unique perspective for fabricating MCF devices and boosting various MCF applications.
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A tunable fiber polarizer based on the selectively silver-coated large-core suspended-core fiber (LSCF) was proposed. A thin silver layer was coated on the inner surface of two opposite air holes of the LSCF by the chemical liquid-phase deposition method. The $y$-polarized light (parallel to the two silver-coated air holes) will excite surface plasmon resonance and experience large transmission loss, while the $x$-polarized light does not, resulting in a fiber polarizer. By varying the liquid filled in the microchannels of the LSCF, the operating wavelength can be tuned in the visible and near infrared region along with the surface plasmon resonance wavelength. The dependence of the polarization characteristics on the fiber length was experimentally investigated. The maximum polarization extinction ratio (PER) of 20.1 dB, 19.6 dB, and 18.3 dB and insertion loss (IL) of 2.24 dB, 2.56 dB, and 2.08 dB are achieved with the optimal fiber length of 16 cm at the operating wavelengths of 565.4 nm, 626.7 nm, and 739.7 nm, respectively. Compared with the multimode fiber-based polarizers reported previously, the proposed selectively silver-coated LSCF polarizer exhibits higher PER and lower IL.
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Intraoperative internal carotid artery injury is one of the most daunting complications in endoscopic skull base surgery. This paper proposed a novel technique to manage ICA injury after proximal and distal controls. The appropriate block sites together with the proximal and distal controls of ICA were demonstrated in six injected cadaveric specimens. The surgical outcomes of five patients with intraoperative ICA injury and managed with this concept were retrospectively reviewed. Five block sites for vascular control could be identified in all six specimens, including (1) distal to the distal dural ring, (2) proximal to the proximal dural ring, (3) anterior genu of the parasellar ICA, (4) the upper third of the paraclival ICA, and (5) just above the foramen lacerum. Both proximal and distal controls of ICA were achieved by using the block sites in combination. Gross tumor resection was achieved in all five cases after the intraoperative ICA injury was successfully managed. Three coping techniques were used, including direct coagulation to seal (three cases), endoscopic suture (one case), and coagulation to sacrifice (one case). Focal brainstem infarction occurred in one case, one patient died of intracranial infection, and the other three cases had no sequelae. No pseudoaneurysm occurred in all patients. Except the sacrificed ICA, the other ICA was intact during follow-up. It is technically feasible to manage ICA injuries after proximal and distal controls during EEA surgeries. The surgical outcomes from our case series supported the use of this novel technique.
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Lesões das Artérias Carótidas , Artéria Carótida Interna , Lesões das Artérias Carótidas/etiologia , Lesões das Artérias Carótidas/cirurgia , Artéria Carótida Interna/cirurgia , Humanos , Procedimentos Neurocirúrgicos , Estudos Retrospectivos , Base do Crânio/cirurgiaRESUMO
Fiber gas sensing techniques have been applied for a wide range of industrial applications. In this paper, the basic fiber gas sensing principles and the development of different fibers have been introduced. In various specialty fibers, hollow-core photonic crystal fibers (HC-PCFs) can overcome the fundamental limits of solid fibers and have attracted intense interest recently. Here, we focus on the review of HC-PCF gas sensing, including the light-guiding mechanisms of HC-PCFs, various sensing configurations, microfabrication approaches, and recent research advances including the mid-infrared gas sensors via hollow core anti-resonant fibers. This review gives a detailed and deep understanding of HC-PCF gas sensors and will promote more practical applications of HC-PCFs in the near future.
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Angiogenesis is a major pathologic characteristic of glioblastoma, which is one aggressive primary brain tumor. MicroRNA-221/222 (miR-221/222) cluster has been previously reported to function importantly in malignant glioma biological process. The current study aims at evaluating the effects of miR-221/222 cluster on angiogenesis of glioblastoma cells. Microarray data were analyzed to select glioblastoma-associated differentially expressed genes, and dual-luciferase reporter assay was performed to assess targeting correlation between miR-221/222 cluster and suppressor of cytokine signaling-3 (SOCS3). Subsequently, the expression patterns of miR-221 and miR-222 in glioblastoma cells were identified. miR-221 and miR-222 were overexpressed or silenced in glioblastoma cells to identify the effect of miR-221/222 cluster in cell invasion, migration, proliferation, and angiogenesis. To define downstream pathway of miR-221/222 cluster or SOCS3 in glioblastoma, levels of Janus kinase (JAK)/signal transducers and activators of transcription (STAT) pathway-related proteins were assessed. Additionally, the functions of miR-221/222 on glioblastoma cell angiogenesis were measured in vivo with microvessel density assayed. miR-221 and miR-222 were expressed at a high level and SOCS3 was at a low level in glioblastoma. Downregulation of the miR-221/222 cluster diminished the invasion, migration, proliferation, and angiogenesis with reduced protein levels of matrix metalloproteinase-2 (MMP-2), MMP-9, and vascular endothelial growth factor in glioblastoma cells. Also, silencing miR-221/222 cluster reduced p-JAK2/JAK2 and p-STAT3/STAT3. Consistently, the inhibitory role of silencing miR-221/222 cluster on tumorigenesis of glioblastoma cells was confirmed in vivo. Collectively, the inhibition of miR-221/222 cluster could attenuate the glioblastoma angiogenesis through inactivation of the JAK/STAT pathway by upregulating SOCS3.
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Inativação Gênica , Glioblastoma/irrigação sanguínea , Janus Quinases/metabolismo , MicroRNAs/metabolismo , Neovascularização Patológica/genética , Fatores de Transcrição STAT/metabolismo , Proteína 3 Supressora da Sinalização de Citocinas/metabolismo , Animais , Sequência de Bases , Carcinogênese/genética , Carcinogênese/patologia , Linhagem Celular Tumoral , Movimento Celular/genética , Proliferação de Células/genética , Regulação para Baixo/genética , Regulação Neoplásica da Expressão Gênica , Células Endoteliais da Veia Umbilical Humana/metabolismo , Humanos , Camundongos Nus , MicroRNAs/genética , Modelos Biológicos , Família Multigênica , Invasividade Neoplásica , Neovascularização Patológica/patologia , Transdução de Sinais , Regulação para Cima/genéticaRESUMO
We present a novel and efficient approach to generating Bessel-like beams through fabricating self-growing polymer microtips at the facet of single-mode fibers. To produce these beams, the length and shape of microtips were precisely optimized. Specifically, the convex droplet height and its photopolymerization parameters feature prominently in Bessel-like beams via microtips. A wide conversion bandwidth of the microtips and self-healing properties of the produced Bessel-like beam were also investigated in detail. Our microtips provide an effective, low-cost, and ultra-compact way for Bessel-like beams generation.
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We demonstrate the first, to the best of our knowledge, photothermal carbon monoxide (CO) sensor using a hollow-core negative curvature fiber. The hollow-core fiber features a typical structure of one ring cladding containing eight nontouching capillaries to form a negative curvature core-surround. The photothermal effect in a 40-µm hollow core is induced by CO absorption at 2327 nm and detected by a Mach-Zehnder interferometer operating at 1533 nm. By using wavelength modulation spectroscopy, we achieve a normalized noise equivalent absorption coefficient of 4.4×10-8 cm-1 WHz-1/2. As CO has a very slow vibrational-translational relaxation process, we enhance the photothermal signal by enhancing the relaxation with the water vapor additive.
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We correct an error of the nonlinear refractive index used in our original paper.
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The photoinduced regio- and enantioselective coupling of naphthols and derivatives thereof is achieved in the confined chiral coordination space of a RuII metalloligand based cage. The racemic or enantiopure cages encapsulate naphthol guests, which then undergo a regiospecific 1,4-coupling, rather than the normal 1,1-coupling, to form 4-(2-hydroxy-1-naphthyl)-1,2-napthoquinones; moderate stereochemical control is achieved with homochiral cages. The photoreactions proceed under both aerobic and anaerobic conditions but through distinct pathways that nevertheless involve the same radical intermediates. This unusual dimerization constitutes a very rare example of asymmetric induction in biaryl coupling by making use of coordination cages with dual functionality-photoredox reactivity and stereoselectivity.
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In recent years, it has been widely identified that the stromal cell-derived factor 1 (SDF-1) and anterior gradient 2 (AGR2) were implicated in the development of epithelial-mesenchymal transition (EMT) in a variety of cancers. However, the involvement of SDF-1-AGR2 pathway in the EMT of glioblastoma has not been investigated. In the present study, the in vitro assays were used to investigate the role of AGR2 in cell cycle, migration, and invasion. We found that the expressions of AGR2 and chemokine (C-X-C motif) receptor 4 (CXCR4) were obviously upregulated in glioblastoma cells T98G, A172, U87, and U251 than those in normal human astrocytes (NHA) (all p < 0.01), among which both U87 and U251 cells presented the highest expression (p > 0.05). Western blot revealed that SDF-1 induced the expression of p-AKT, AGR2, and EMT markers (N-cadherin, matrix metalloproteinase-2 (MMP2), and Slug) in a dose-dependent manner in U87 and U251 cells. However, the depletion of AGR2 reversed SDF-1-induced upregulation of EMT markers rather than p-AKT. Furthermore, functional analysis identified that knockdown of AGR2 induced cell cycle arrest in G0/G1 phase and suppressed the migration and invasion of U87 and U251 cells. Taken together, SDF-1-CXCR4 pathway induced the expression of AGR2 to control the progression of EMT likely via AKT pathway in the development of glioblastoma. Our findings lay a promising foundation for the SDF-1-AGR2 axis-targeting therapy in patients with glioblastoma.