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      CCL4‐mediated targeting of spleen tyrosine kinase (Syk) inhibitor using nanoparticles alleviates inflammatory bowel disease

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          Abstract

          Inflammatory bowel disease (IBD) has emerged a global disease and the ascending incidence and prevalence is accompanied by elevated morbidity, mortality, and substantial healthcare system costs. However, the current typical one‐size‐fits‐all therapeutic approach is suboptimal for a substantial proportion of patients due to the variability in the course of IBD and a considerable number of patients do not have positive response to the clinically approved drugs, so there is still a great, unmet demand for novel alternative therapeutic approaches. Spleen tyrosine kinase (Syk), a cytoplasmic nonreceptor protein tyrosine kinase, plays crucial roles in signal transduction and there are emerging data implicating that Syk participates in pathogenesis of several gut disorders, such as IBD. In this study, we observed the Syk expression in IBD patients and explored the effects of therapeutic Syk inhibition using small‐molecule Syk inhibitor piceatannol in bone marrow–derived macrophages (BMDMs). In addition, due to the poor bioavailability and pharmacokinetics of small‐molecule tyrosine kinase inhibitors and superiority of targeting nanoparticles‐based drug delivery system, we herein prepared piceatannol‐encapsulated poly(lactic‐co‐glycolic acid) nanoparticles that conjugated with chemokine C–C motif ligand 4 (P‐NPs‐C) and studied its therapeutic effects in vitro in BMDMs and in vivo in experimental colitis model. Our results indicated that in addition to alleviating colitis, oral administration of P‐NPs‐C promoted the restoration of intestinal barrier function and improved intestinal microflora dysbiosis, which represents a promising treatment for IBD.

          Abstract

          1. The expression level of Syk increased in inflamed colon mucosa tissues from IBD patients and was associated with disease activity.

          2. Piceatannol‐encapsulated poly(lactic‐co‐glycolic acid) nanoparticles that conjugated with chemokine CCL4 (P‐NPs‐C) alleviates experimental colitis.

          3. Oral administration of P‐NPs‐C promotes the restoration of intestinal barrier function and improves intestinal microflora dysbiosis.

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          Most cited references46

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          Worldwide incidence and prevalence of inflammatory bowel disease in the 21st century: a systematic review of population-based studies.

          Inflammatory bowel disease is a global disease in the 21st century. We aimed to assess the changing incidence and prevalence of inflammatory bowel disease around the world.
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            Poly Lactic-co-Glycolic Acid (PLGA) as Biodegradable Controlled Drug Delivery Carrier.

            In past two decades poly lactic-co-glycolic acid (PLGA) has been among the most attractive polymeric candidates used to fabricate devices for drug delivery and tissue engineering applications. PLGA is biocompatible and biodegradable, exhibits a wide range of erosion times, has tunable mechanical properties and most importantly, is a FDA approved polymer. In particular, PLGA has been extensively studied for the development of devices for controlled delivery of small molecule drugs, proteins and other macromolecules in commercial use and in research. This manuscript describes the various fabrication techniques for these devices and the factors affecting their degradation and drug release.
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              Gut microbiota and IBD: causation or correlation?

              A general consensus exists that IBD is associated with compositional and metabolic changes in the intestinal microbiota (dysbiosis). However, a direct causal relationship between dysbiosis and IBD has not been definitively established in humans. Findings from animal models have revealed diverse and context-specific roles of the gut microbiota in health and disease, ranging from protective to pro-inflammatory actions. Moreover, evidence from these experimental models suggest that although gut bacteria often drive immune activation, chronic inflammation in turn shapes the gut microbiota and contributes to dysbiosis. The purpose of this Review is to summarize current associations between IBD and dysbiosis, describe the role of the gut microbiota in the context of specific animal models of colitis, and discuss the potential role of microbiota-focused interventions in the treatment of human IBD. Ultimately, more studies will be needed to define host–microbial relationships relevant to human disease and amenable to therapeutic interventions.
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                Author and article information

                Contributors
                lygwxw@163.com
                zhaoyun056@gmail.com
                jiananr@gmail.com
                Journal
                Clin Transl Med
                Clin Transl Med
                10.1002/(ISSN)2001-1326
                CTM2
                Clinical and Translational Medicine
                John Wiley and Sons Inc. (Hoboken )
                2001-1326
                17 February 2021
                February 2021
                : 11
                : 2 ( doiID: 10.1002/ctm2.v11.2 )
                : e339
                Affiliations
                [ 1 ] School of Medicine, Southeast University, Research Institute of General Surgery Jinling Hospital Nanjing China
                [ 2 ] Research Institute of General Surgery Jinling Hospital Nanjing China
                [ 3 ] Department of General Surgery, BenQ Medical Center The Affiliated BenQ Hospital of Nanjing Medical University Nanjing China
                Author notes
                [*] [* ] Correspondence

                Xiuwen Wu, Research Institute of General Surgery, Jinling Hospital, 305 East Zhongshan Road, Nanjing 210002, Jiangsu Province, China.

                Email: lygwxw@ 123456163.com

                Yun Zhao, Department of General Surgery, BenQ Medical Center, The Affiliated BenQ Hospital of Nanjing Medical University, Nanjing, China.

                Email: zhaoyun056@ 123456gmail.com

                Jianan Ren, School of Medicine, Southeast University, Research Institute of General Surgery, Jinling Hospital, 305 East Zhongshan Road, Nanjing 210002, Jiangsu Province, China.

                Email: jiananr@ 123456gmail.com

                Author information
                https://orcid.org/0000-0002-4697-4762
                Article
                CTM2339
                10.1002/ctm2.339
                7888545
                33634985
                d0888a49-4f26-4f81-a73f-5ab0d846432c
                © 2021 The Authors. Clinical and Translational Medicine published by John Wiley & Sons Australia, Ltd on behalf of Shanghai Institute of Clinical Bioinformatics

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 02 December 2020
                : 01 February 2021
                : 07 February 2021
                Page count
                Figures: 9, Tables: 0, Pages: 19, Words: 8813
                Funding
                Funded by: National Natural Science Foundation of China , open-funder-registry 10.13039/501100001809;
                Award ID: 82072149
                Funded by: Distinguished Scholars Foundation of Jiangsu Province
                Award ID: JCRCB2016006
                Funded by: Innovation Project of Military Medicine
                Award ID: 16CXZ007
                Funded by: General Project of Military Logistics Research
                Award ID: CLB19J025
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                February 2021
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.9.7 mode:remove_FC converted:17.02.2021

                Medicine
                ccl4,inflammatory bowel disease,piceatannol,syk
                Medicine
                ccl4, inflammatory bowel disease, piceatannol, syk

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