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  • Jia, Fan  (332)
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  • 1
    In: Advanced Functional Materials, Wiley, Vol. 33, No. 30 ( 2023-07)
    Abstract: Vascular restenosis after balloon dilation is largely caused by the over‐proliferation of smooth muscle cells, which is triggered and exacerbated by local excessive inflammation and oxidative stress. The excessive inflammatory and oxidative stress cause tissue/cell damage, hamper endothelial functions, and worsen intimal hyperplasia and restenosis. A high level of reactive oxygen species (ROS) overproduction is regarded as the main culprit. Therefore, efficiently inhibiting ROS over‐production or weightily depleting them is of great significance. Herein, a “ROS‐responsive/scavenging prodrug” is introduced into balloon coating for the treatment of vascular restenosis. A reversible phenylboronic ester‐bearing caffeic acid (CA) macromolecular prodrug (PBC) is designed for the controlled and on‐demand dual‐drug release triggered by the local high ROS level; the released CA and 4‐hydroxybenzyl alcohol exhibit efficient antioxidant and anti‐inflammatory effects by scavenging ROS, thereby regulating vascular microenvironment and protecting endothelium functions. To accelerate endothelium regeneration, pro‐endothelial microRNA‐126 is further introduced. The ROS‐responsive/scavenging prodrug/miRNA balloon coating efficiently prevents intimal hyperplasia, alleviates local inflammation, and improves endothelium healing in a rat abdominal aorta restenosis model, which may provide applicative perspectives for next‐generation drug‐coated balloons and other cardiovascular diseases treatment.
    Type of Medium: Online Resource
    ISSN: 1616-301X , 1616-3028
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2023
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  • 2
    Online Resource
    Online Resource
    American Association for the Advancement of Science (AAAS) ; 2019
    In:  Science Vol. 363, No. 6430 ( 2019-03)
    In: Science, American Association for the Advancement of Science (AAAS), Vol. 363, No. 6430 ( 2019-03)
    Abstract: The El Niño–Southern Oscillation (ENSO), which originates in the Pacific, is the strongest and most well-known mode of tropical climate variability. Its reach is global, and it can force climate variations of the tropical Atlantic and Indian Oceans by perturbing the global atmospheric circulation. Less appreciated is how the tropical Atlantic and Indian Oceans affect the Pacific. Especially noteworthy is the multidecadal Atlantic warming that began in the late 1990s, because recent research suggests that it has influenced Indo-Pacific climate, the character of the ENSO cycle, and the hiatus in global surface warming. Discovery of these pantropical interactions provides a pathway forward for improving predictions of climate variability in the current climate and for refining projections of future climate under different anthropogenic forcing scenarios.
    Type of Medium: Online Resource
    ISSN: 0036-8075 , 1095-9203
    RVK:
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    Language: English
    Publisher: American Association for the Advancement of Science (AAAS)
    Publication Date: 2019
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  • 3
    In: Science Bulletin, Elsevier BV, Vol. 68, No. 9 ( 2023-05), p. 946-960
    Type of Medium: Online Resource
    ISSN: 2095-9273
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2023
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  • 4
    In: The Journal of Neuroscience, Society for Neuroscience, Vol. 37, No. 47 ( 2017-11-22), p. 11335-11352
    Abstract: Group 1 metabotropic glutamate receptors (mGlu1/5s) are critical to synapse formation and participate in synaptic LTP and LTD in the brain. mGlu1/5 signaling alterations have been documented in cognitive impairment, neurodegenerative disorders, and psychiatric diseases, but underlying mechanisms for its modulation are not clear. Here, we report that transferrin receptor 1 (TFR1), a transmembrane protein of the clathrin complex, modulates the trafficking of mGlu1 in cerebellar Purkinje cells (PCs) from male mice. We show that conditional knock-out of TFR1 in PCs does not affect the cytoarchitecture of PCs, but reduces mGlu1 expression at synapses. This regulation by TFR1 acts in concert with that by Rab8 and Rab11, which modulate the internalization and recycling of mGlu1, respectively. TFR1 can bind to Rab proteins and facilitate their expression at synapses. PC ablation of TFR1 inhibits parallel fiber–PC LTD, whereas parallel fiber–LTP and PC intrinsic excitability are not affected. Finally, we demonstrate that PC ablation of TFR1 impairs motor coordination, but does not affect social behaviors in mice. Together, these findings underscore the importance of TFR1 in regulating mGlu1 trafficking and suggest that mGlu1- and mGlu1-dependent parallel fiber–LTD are associated with regulation of motor coordination, but not autistic behaviors. SIGNIFICANCE STATEMENT Group 1 metabotropic glutamate receptor (mGlu1/5) signaling alterations have been documented in cognitive impairment, neurodegenerative disorders, and psychiatric diseases. Recent work suggests that altered mGlu1 signaling in Purkinje cells (PCs) may be involved in not only motor learning, but also autistic-like behaviors. We find that conditional knock-out of transferrin receptor 1 (TFR1) in PCs reduces synaptic mGlu1 by tethering Rab8 and Rab11 in the cytosol. PC ablation of TFR1 inhibits parallel fiber–PC LTD, whereas parallel fiber–PC LTP and PC intrinsic excitability are intact. Motor coordination is impaired, but social behaviors are normal in TFR1 flox/flox ;pCP2-cre mice. Our data reveal a new regulator for trafficking and synaptic expression of mGlu1 and suggest that mGlu1-dependent LTD is associated with motor coordination, but not autistic-like behaviors.
    Type of Medium: Online Resource
    ISSN: 0270-6474 , 1529-2401
    Language: English
    Publisher: Society for Neuroscience
    Publication Date: 2017
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  • 5
    In: Biomaterials, Elsevier BV, Vol. 292 ( 2023-01), p. 121919-
    Type of Medium: Online Resource
    ISSN: 0142-9612
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2023
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    SSG: 12
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  • 6
    Online Resource
    Online Resource
    American Geophysical Union (AGU) ; 2020
    In:  Journal of Geophysical Research: Oceans Vol. 125, No. 12 ( 2020-12)
    In: Journal of Geophysical Research: Oceans, American Geophysical Union (AGU), Vol. 125, No. 12 ( 2020-12)
    Abstract: Vertical structure of currents in the upper 800 m off the New Guinea coast is revealed with mooring measurements Monsoon‐induced seasonality is not trapped in upper ocean, a seasonally reversing flow is detected below New Guinea Coastal Undercurrent (NGCUC) Velocity core of NGCUC shoals/deepens in El Nino/La Nina, the transport shows no significant relation with ENSO
    Type of Medium: Online Resource
    ISSN: 2169-9275 , 2169-9291
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 2020
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    detail.hit.zdb_id: 161667-5
    detail.hit.zdb_id: 3094219-6
    SSG: 16,13
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  • 7
    Online Resource
    Online Resource
    American Geophysical Union (AGU) ; 2018
    In:  Journal of Geophysical Research: Oceans Vol. 123, No. 7 ( 2018-07), p. 4874-4887
    In: Journal of Geophysical Research: Oceans, American Geophysical Union (AGU), Vol. 123, No. 7 ( 2018-07), p. 4874-4887
    Abstract: Spatial structure of oceanic ISV in the Philippine Sea is investigated with multisource observations and numerical simulations Mesoscale eddies and Rossby waves related to dynamic instability are major sources of oceanic ISV in the Philippine Sea MJO contributes half of the total observed ISV and acts in forming the ISV features in the Philippine Sea
    Type of Medium: Online Resource
    ISSN: 2169-9275 , 2169-9291
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 2018
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    detail.hit.zdb_id: 161667-5
    detail.hit.zdb_id: 3094219-6
    SSG: 16,13
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  • 8
    Online Resource
    Online Resource
    Elsevier BV ; 2013
    In:  Virologica Sinica Vol. 28, No. 1 ( 2013-2), p. 16-23
    In: Virologica Sinica, Elsevier BV, Vol. 28, No. 1 ( 2013-2), p. 16-23
    Type of Medium: Online Resource
    ISSN: 1674-0769 , 1995-820X
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2013
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  • 9
    Online Resource
    Online Resource
    American Society of Clinical Oncology (ASCO) ; 2019
    In:  Journal of Clinical Oncology Vol. 37, No. 15_suppl ( 2019-05-20), p. e15665-e15665
    In: Journal of Clinical Oncology, American Society of Clinical Oncology (ASCO), Vol. 37, No. 15_suppl ( 2019-05-20), p. e15665-e15665
    Abstract: e15665 Background: Immune checkpoint blockade (ICB) has delivered unprecedented success in treating patients with metastatic cancers to extend overall survival, yet only a small percentage of patients respond. Immune-relevant genomic biomarkers, such as tumor mutation burden (TMB), neoantigen, and human leukocyte antigen class I (HLA-I) are emerging as potential predictors for immunotherapy response. However, little is known about their heterogeneity in metastatic cancer patients. In this study, we aim to characterize these immune-relevant genomic biomarkers in primary and matched metastatic hepatocellular carcinoma (HCC). Methods: Two cohorts of samples were included in this study. Cohort 1: a total of 24 pairs of surgical resected primary and matched metastatic HCC tissue. Cohort 2: 29 surgical resected primary HCC tissue from patients with long-term relapse-free survival. All samples were characterized using whole exome sequencing and RNA sequencing. We compared TMB, neoantigen and HLA-I genotype between primary and matched metastatic tumors, as well as between primary tumors with or without postoperative metastatic relapse. Results: The TMB of primary HCC with metastatic relapse was significantly higher than that with long-term relapse-free survival (Mean, 32 vs 17 mutations/Mb, P 〈 0.05), while neoantigen and HLA-I genotype failed to show statistical difference. Paired comparison between primary and matched metastatic tumors indicated that both TMB and neoantigen were significantly decreased in metastases ( P 〈 0.05). We further categorized metastases into two subgroups based on their HLA-I genotype. HLA-I homozygosity in at least one locus (homozygous) occurred in 9 metastases, while the rest metastases showed maximal heterozygosity at HLA-loci (heterozygous). HLA-I heterozygous metastases were associated with significantly higher neoantigen load compared with HLA-I homozygous metastases ( P 〈 0.05). Conclusions: High TMB might be a poor prognostic factor in patients with resected HCC and a potential predictor for postoperative adjuvant therapy with ICB. Metastatic HCC showed lower antigenicity than the corresponding primary tumors. Therefore, they might not show the same responsiveness to immunotherapy as primary tumor did. However, our HLA-I genotype analysis provides evidence that HLA-I heterozygosity has potential implication for predicting response of metastatic HCC to ICB.
    Type of Medium: Online Resource
    ISSN: 0732-183X , 1527-7755
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    Language: English
    Publisher: American Society of Clinical Oncology (ASCO)
    Publication Date: 2019
    detail.hit.zdb_id: 2005181-5
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  • 10
    Online Resource
    Online Resource
    American Society of Clinical Oncology (ASCO) ; 2019
    In:  Journal of Clinical Oncology Vol. 37, No. 4_suppl ( 2019-02-01), p. 246-246
    In: Journal of Clinical Oncology, American Society of Clinical Oncology (ASCO), Vol. 37, No. 4_suppl ( 2019-02-01), p. 246-246
    Abstract: 246 Background: The transcriptional heterogeneity and immune evasion mechanisms of CTCs during systemic circulation are not well defined. Methods: Blood was drawn from 4 different vascular sites, including hepatic vein (HV), peripheral artery (PA), peripheral vein (PV) and portal vein (PoV) of 10 localized HCC patients. Single CTCs were isolated by negative enrichment and robotic micromanipulator, followed by single-cell RNA-sequencing (sc-RNAseq). After filtering, 113 CTCs with qualified data remained were subjected to further bioinformatics analysis. The scRNA-seq results were further validated in three independent cohorts of HCC patients. Results: Our scRNA-seq data revealed remarkable intra- and inter-vascular heterogeneity among CTCs from four vascular sites. We determined CTC transcriptional dynamics during transportation through consecutive vascular compartments and revealed their adaptation mechanisms under biomechanical stress during circulation. We further classified CTCs from different vascular sites into two subsets, namely dormant CTCs and activated CTCs. Dormant CTCs were associated with a non-cycling state and upregulation of EMT/angiogenic signatures and showed stronger prognostic ability for early recurrence than activated CTCs did. Furthermore, we discovered an immune escape mechanism by which CTCs recruited regulatory T cells (Tregs) via expression of CCL5, consequently promoting the formation of an immunosuppressive microenvironment favorable for their survival in the bloodstream and seeding in secondary organs. We proved that MAX, activated through the p38 pathway, was the key transcriptional factor regulating CCL5 overexpression, which was validated by ChIP, luciferase reporter gene and in vitro/vivo knockdown assays. And we further determined that Tregs-derived TGF-β1 can heighten MAX expression, thus amplifying the CCL5 expression. Conclusions: Collectively, our results reveal a previously unappreciated spatial heterogeneity of CTCs and a CTC immune-escape mechanism, which may aid in designing new anti-metastasis therapeutic strategies in HCC.
    Type of Medium: Online Resource
    ISSN: 0732-183X , 1527-7755
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    Language: English
    Publisher: American Society of Clinical Oncology (ASCO)
    Publication Date: 2019
    detail.hit.zdb_id: 2005181-5
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