RESUMO
The current accuracy of speech recognition can reach over 97% on different datasets, but in noisy environments, it is greatly reduced. Improving speech recognition performance in noisy environments is a challenging task. Due to the fact that visual information is not affected by noise, researchers often use lip information to help to improve speech recognition performance. This is where the performance of lip recognition and the effect of cross-modal fusion are particularly important. In this paper, we try to improve the accuracy of speech recognition in noisy environments by improving the lip reading performance and the cross-modal fusion effect. First, due to the same lip possibly containing multiple meanings, we constructed a one-to-many mapping relationship model between lips and speech allowing for the lip reading model to consider which articulations are represented from the input lip movements. Audio representations are also preserved by modeling the inter-relationships between paired audiovisual representations. At the inference stage, the preserved audio representations could be extracted from memory by the learned inter-relationships using only video input. Second, a joint cross-fusion model using the attention mechanism could effectively exploit complementary intermodal relationships, and the model calculates cross-attention weights on the basis of the correlations between joint feature representations and individual modalities. Lastly, our proposed model achieved a 4.0% reduction in WER in a -15 dB SNR environment compared to the baseline method, and a 10.1% reduction in WER compared to speech recognition. The experimental results show that our method could achieve a significant improvement over speech recognition models in different noise environments.
Assuntos
Leitura Labial , Percepção da Fala , Humanos , Fala , Aprendizagem , LábioRESUMO
Parkinson's disease (PD) is characterized by the accumulation of misfolded α-synuclein protein and the loss of dopaminergic neurons in the substantia nigra. Abnormal α-synuclein aggregates form toxic Lewy bodies, ultimately inducing neuronal injury. Mitochondrial dysfunction was reported to be involved in the neurotoxicity of α-synuclein aggregates in PD. However, the specific mechanism by which abnormal α-synuclein aggregates cause mitochondrial disorders remains poorly defined. Previously, we found that cofilin-1, a member of the actin-binding protein, regulates α-synuclein pathogenicity by promoting its aggregation and spreading in vitro and in vivo. In this study, we further investigated the effect of cofilin-1 on α-synuclein induced mitochondrial damage. We discovered that α-synuclein aggregates accelerate the translocation of cofilin-1 to mitochondria, promote its combination with the mitochondrial outer membrane receptor Tom 20, and ultimately activate the oxidative damage and apoptosis pathway in mitochondria. All these results demonstrate the important regulatory role of cofilin-1 in the mitochondrial neurotoxicity of pathological α-synuclein during the progression of PD.
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Autogenous bone transplantation is a prevalent clinical method for addressing bone defects. However, the limited availability of donor bone and the morbidity associated with bone harvesting have propelled the search for suitable bone substitutes. Bio-inspired scaffolds, particularly those fabricated using electron beam melting (EBM) deposition technology, have emerged as a significant advancement in this field. These 3D-printed titanium alloy scaffolds are celebrated for their outstanding biocompatibility and favorable elastic modulus. Thermosensitive chitosan hydrogel, which transitions from liquid to solid at body temperature, serves as a popular carrier in bone tissue engineering. Icariin (ICA), known for its efficacy in promoting osteoblast differentiation from bone marrow mesenchymal stem cells (BMSCs), plays a crucial role in this context. We developed a system combining a 3D-printed titanium alloy with a thermosensitive chitosan hydrogel, capable of local bone regeneration and integration through ICA delivery. Our in vitro findings reveal that this system can gradually release ICA, demonstrating excellent biocompatibility while fostering BMSC proliferation and osteogenic differentiation. Immunohistochemistry and Micro-CT analyses further confirm the effectiveness of the system in accelerating in vivo bone regeneration and enhancing osseointegration. This composite system lays a significant theoretical foundation for advancing local bone regeneration and integration.
Assuntos
Ligas , Diferenciação Celular , Quitosana , Flavonoides , Hidrogéis , Células-Tronco Mesenquimais , Osseointegração , Osteogênese , Impressão Tridimensional , Alicerces Teciduais , Titânio , Quitosana/química , Quitosana/farmacologia , Titânio/química , Osseointegração/efeitos dos fármacos , Ligas/química , Ligas/farmacologia , Alicerces Teciduais/química , Animais , Células-Tronco Mesenquimais/efeitos dos fármacos , Células-Tronco Mesenquimais/citologia , Osteogênese/efeitos dos fármacos , Hidrogéis/química , Hidrogéis/farmacologia , Diferenciação Celular/efeitos dos fármacos , Proliferação de Células/efeitos dos fármacos , Regeneração Óssea/efeitos dos fármacos , Engenharia Tecidual/métodosRESUMO
At present, bone nonunion and delayed union are still difficult problems in orthopaedics. Since the discovery of bone morphogenetic protein (BMP), it has been widely used in various studies due to its powerful role in promoting osteogenesis and chondrogenesis. Current results show that BMPs can promote healing of bone defects and reduce the occurrence of complications. However, the mechanism of BMP in vivo still needs to be explored, and application of BMP alone to a bone defect site cannot achieve good therapeutic effects. It is particularly important to modify implants to carry BMP to achieve slow and sustained release effects by taking advantage of the nature of the implant. This review aims to explain the mechanism of BMP action in vivo, its biological function, and how BMP can be applied to orthopaedic implants to effectively stimulate bone healing in the long term. Notably, implantation of a system that allows sustained release of BMP can provide an effective method to treat bone nonunion and delayed bone healing in the clinic.
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Tumor resection and treatment of trauma-related regional large bone defects have major challenges in the field of orthopedics. Scaffolds that treat bone defects are the focus of bone tissue engineering. 3D printing porous titanium alloy scaffolds, prepared via electron beam melting technology, possess customized structure and strength. The addition of a growth factor coating to the scaffold introduces a specific form of biological activation. Vascular endothelial growth factor (VEGF) is key to angiogenesis and osteogenesis in vivo. We designed a porous titanium alloy scaffold/thermosensitive collagen hydrogel system, equipped with VEGF, to promote local osseointegration and angiogenesis. We also verified the VEGF release via thermosensitive collagen and proliferation and induction of the human umbilical vein endothelial cells (HUVECs) via the composite system in vitro. In vivo, using microscopic computed tomography (Micro-CT), histology, and immunohistochemistry analysis, we confirmed that the composite scaffold aids in angiogenesis-mediated bone regeneration, and promotes significantly more bone integration. We also discovered that the composite scaffold has excellent biocompatibility, provides bioactive VEGF for angiogenesis and osteointegration, and provides an important theoretical basis for the restoration of local blood supply and strengthening of bone integration.
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BACKGROUND: The international invasive and quarantined defoliating insect Hyphantria cunea Drury (Lepidoptera: Arctiidae) causes huge ecological and economic losses in the world. Furthermore, future climate change may alter the distribution of H. cunea and aggravate the damage. In the present study, we used CLIMEX to project the potential global distribution of H. cunea according to both historical climate data (1961-1990) and future climate warming estimates (2011-2100) to define the impact of climate change. RESULTS: Under the historical climate scenario, we found that H. cunea can survive on every continent, and temperature is the main factor that limits its establishment. With climate change, suitability will increase in middle and high latitude regions, while decrease in the low latitude regions. Moreover, tropic regions will be the most sensitive to climate change impacts for the pest to survive. The impacts of climate change will also increase over time, whether they be positive impacts or negative impacts. CONCLUSION: The projected potential distributions provide a theoretical basis for quarantine and control strategies for the management of this pest in each country. Furthermore, these results provide substantial guidance for studies of the effects of climate change on other major forest pests. © 2018 Society of Chemical Industry.