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      LDL receptor-related protein 1 (LRP1), a novel target for opening the blood-labyrinth barrier (BLB)

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          Abstract

          Inner ear disorders are a cluster of diseases that cause hearing loss in more than 1.5 billion people worldwide. However, the presence of the blood-labyrinth barrier (BLB) on the surface of the inner ear capillaries greatly hinders the effectiveness of systemic drugs for prevention and intervention due to the low permeability, which restricts the entry of most drug compounds from the bloodstream into the inner ear tissue. Here, we report the finding of a novel receptor, low-density lipoprotein receptor-related protein 1 (LRP1), that is expressed on the BLB, as a potential target for shuttling therapeutics across this barrier. As a proof-of-concept, we developed an LRP1-binding peptide, IETP2, and covalently conjugated a series of model small-molecule compounds to it, including potential drugs and imaging agents. All compounds were successfully delivered into the inner ear and inner ear lymph, indicating that targeting the receptor LRP1 is a promising strategy to enhance the permeability of the BLB. The discovery of the receptor LRP1 will illuminate developing strategies for crossing the BLB and for improving systemic drug delivery for inner ear disorders.

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          Genome-scale CRISPR-Cas9 knockout screening in human cells.

          The simplicity of programming the CRISPR (clustered regularly interspaced short palindromic repeats)-associated nuclease Cas9 to modify specific genomic loci suggests a new way to interrogate gene function on a genome-wide scale. We show that lentiviral delivery of a genome-scale CRISPR-Cas9 knockout (GeCKO) library targeting 18,080 genes with 64,751 unique guide sequences enables both negative and positive selection screening in human cells. First, we used the GeCKO library to identify genes essential for cell viability in cancer and pluripotent stem cells. Next, in a melanoma model, we screened for genes whose loss is involved in resistance to vemurafenib, a therapeutic RAF inhibitor. Our highest-ranking candidates include previously validated genes NF1 and MED12, as well as novel hits NF2, CUL3, TADA2B, and TADA1. We observe a high level of consistency between independent guide RNAs targeting the same gene and a high rate of hit confirmation, demonstrating the promise of genome-scale screening with Cas9.
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            Development and applications of CRISPR-Cas9 for genome engineering.

            Recent advances in genome engineering technologies based on the CRISPR-associated RNA-guided endonuclease Cas9 are enabling the systematic interrogation of mammalian genome function. Analogous to the search function in modern word processors, Cas9 can be guided to specific locations within complex genomes by a short RNA search string. Using this system, DNA sequences within the endogenous genome and their functional outputs are now easily edited or modulated in virtually any organism of choice. Cas9-mediated genetic perturbation is simple and scalable, empowering researchers to elucidate the functional organization of the genome at the systems level and establish causal linkages between genetic variations and biological phenotypes. In this Review, we describe the development and applications of Cas9 for a variety of research or translational applications while highlighting challenges as well as future directions. Derived from a remarkable microbial defense system, Cas9 is driving innovative applications from basic biology to biotechnology and medicine. Copyright © 2014 Elsevier Inc. All rights reserved.
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              LRP1 is a master regulator of tau uptake and spread

              Summary The spread of protein aggregates during disease progression is a common theme underlying many neurodegenerative diseases. The microtubule-associated protein tau (MAPT) plays a central role in the pathogenesis of several forms of dementia known as tauopathies, including Alzheimer’s disease (AD), frontotemporal dementia (FTD) and chronic traumatic encephalopathy (CTE) 1 . Progression of these diseases is characterized by the sequential spread and deposition of protein aggregates in a predictable pattern that correlates with clinical severity 2 . This observation and complementary experimental studies 3,4 have suggested that tau can spread in a prion-like manner by passing to naïve cells where it templates misfolding and aggregation. However, while tau propagation has been extensively studied, the underlying cellular mechanisms remain poorly understood. Here we show that the low-density lipoprotein (LDL) receptor-related protein 1 (LRP1) controls tau endocytosis and subsequent spread. Knockdown of LRP1 significantly reduced tau uptake in H4 neuroglioma cells and iPS-derived neurons. The interaction between tau and LRP1 is mediated by lysine residues in the microtubule binding repeat region of tau. Furthermore, we find that downregulation of LRP1 in an in vivo mouse model of tau spread effectively reduced tau propagation between neurons. Our results identify LRP1 as a key regulator of tau spread in the brain and, thus, as a novel target for diseases of tau spread and aggregation.
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                Author and article information

                Contributors
                zhongwu@bmi.ac.cn
                linjian@pku.edu.cn
                shm_yang@163.com
                Journal
                Signal Transduct Target Ther
                Signal Transduct Target Ther
                Signal Transduction and Targeted Therapy
                Nature Publishing Group UK (London )
                2095-9907
                2059-3635
                10 June 2022
                10 June 2022
                2022
                : 7
                : 175
                Affiliations
                [1 ]GRID grid.411642.4, ISNI 0000 0004 0605 3760, Department of Pharmacy, , Peking University Third Hospital, ; Beijing, China
                [2 ]GRID grid.417303.2, ISNI 0000 0000 9927 0537, Artificial Auditory Laboratory of Jiangsu Province, , Xuzhou Medical University, ; Xuzhou, China
                [3 ]GRID grid.410740.6, ISNI 0000 0004 1803 4911, National Engineering Research Center for the Emergency Drug, Beijing Institute of Pharmacology and Toxicology, ; Beijing, China
                [4 ]GRID grid.414252.4, ISNI 0000 0004 1761 8894, College of Otolaryngology Head and Neck Surgery, Chinese PLA General Hospital, ; Beijing, China
                [5 ]National Clinical Research Center for Otolaryngologic Diseases, Beijing, China
                [6 ]GRID grid.419897.a, ISNI 0000 0004 0369 313X, Key Lab of Hearing Science, Ministry of Education, ; Beijing, China
                [7 ]Beijing Key Lab of Hearing Impairment for Prevention and Treatment, Beijing, China
                [8 ]GRID grid.11135.37, ISNI 0000 0001 2256 9319, Synthetic and Functional Biomolecules Center, Beijing National Laboratory for Molecular Sciences, Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry and Molecular Engineering, Innovation Center for Genomics, , Peking University, ; Beijing, China
                Author information
                http://orcid.org/0000-0003-1975-6046
                http://orcid.org/0000-0002-7802-5094
                http://orcid.org/0000-0002-0536-620X
                http://orcid.org/0000-0002-1519-9679
                Article
                995
                10.1038/s41392-022-00995-z
                9184653
                35680846
                9c6947ee-5347-4162-ab69-4f97d5f1d987
                © The Author(s) 2022

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 21 December 2021
                : 16 March 2022
                : 7 April 2022
                Funding
                Funded by: FundRef https://doi.org/10.13039/501100001809, National Natural Science Foundation of China (National Science Foundation of China);
                Award ID: 81800916
                Award ID: 81522046
                Award Recipient :
                Funded by: National Key Research and Development project of China, 2020YFC20052003 National Science and Technology Major Project for Major New drug Innovation and Development,2018ZX09711003 Key International (Regional) Joint Research Program of National Nature Science Foundation of China, 81820108009 The Nature Science Foundation of Xuzhou, KC20177 Jiangsu Provincial University Fund, 19KJA560002
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                © The Author(s) 2022

                target identification,target validation,molecular medicine

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