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

被引:0
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作者
Xi Shi
Zihao Wang
Wei Ren
Long Chen
Cong Xu
Menghua Li
Shiyong Fan
Yuru Xu
Mengbing Chen
Fanjun Zheng
Wenyuan Zhang
Xinbo Zhou
Yue Zhang
Shiwei Qiu
Liyuan Wu
Peng Zhou
Xinze Lv
Tianyu Cui
Yuehua Qiao
Hui Zhao
Weiwei Guo
Wei Chen
Song Li
Wu Zhong
Jian Lin
Shiming Yang
机构
[1] Peking University Third Hospital,Department of Pharmacy
[2] Xuzhou Medical University,Artificial Auditory Laboratory of Jiangsu Province
[3] National Engineering Research Center for the Emergency Drug,Synthetic and Functional Biomolecules Center, Beijing National Laboratory for Molecular Sciences, Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College
[4] Beijing Institute of Pharmacology and Toxicology,undefined
[5] College of Otolaryngology Head and Neck Surgery,undefined
[6] Chinese PLA General Hospital,undefined
[7] National Clinical Research Center for Otolaryngologic Diseases,undefined
[8] Key Lab of Hearing Science,undefined
[9] Ministry of Education,undefined
[10] Beijing Key Lab of Hearing Impairment for Prevention and Treatment,undefined
[11] Peking University,undefined
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摘要
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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