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LDL receptor-related protein 1 (LRP1), a novel target for opening the blood-labyrinth barrier (BLB).
Shi, Xi; Wang, Zihao; Ren, Wei; Chen, Long; Xu, Cong; Li, Menghua; Fan, Shiyong; Xu, Yuru; Chen, Mengbing; Zheng, Fanjun; Zhang, Wenyuan; Zhou, Xinbo; Zhang, Yue; Qiu, Shiwei; Wu, Liyuan; Zhou, Peng; Lv, Xinze; Cui, Tianyu; Qiao, Yuehua; Zhao, Hui; Guo, Weiwei; Chen, Wei; Li, Song; Zhong, Wu; Lin, Jian; Yang, Shiming.
Affiliation
  • Shi X; Department of Pharmacy, Peking University Third Hospital, Beijing, China.
  • Wang Z; Artificial Auditory Laboratory of Jiangsu Province, Xuzhou Medical University, Xuzhou, China.
  • Ren W; National Engineering Research Center for the Emergency Drug, Beijing Institute of Pharmacology and Toxicology, Beijing, China.
  • Chen L; College of Otolaryngology Head and Neck Surgery, Chinese PLA General Hospital, Beijing, China.
  • Xu C; National Clinical Research Center for Otolaryngologic Diseases, Beijing, China.
  • Li M; Key Lab of Hearing Science, Ministry of Education, Beijing, China.
  • Fan S; Beijing Key Lab of Hearing Impairment for Prevention and Treatment, Beijing, China.
  • Xu Y; Department of Pharmacy, Peking University Third Hospital, Beijing, China.
  • Chen M; 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, Chi
  • Zheng F; College of Otolaryngology Head and Neck Surgery, Chinese PLA General Hospital, Beijing, China.
  • Zhang W; National Clinical Research Center for Otolaryngologic Diseases, Beijing, China.
  • Zhou X; Key Lab of Hearing Science, Ministry of Education, Beijing, China.
  • Zhang Y; Beijing Key Lab of Hearing Impairment for Prevention and Treatment, Beijing, China.
  • Qiu S; Artificial Auditory Laboratory of Jiangsu Province, Xuzhou Medical University, Xuzhou, China.
  • Wu L; National Engineering Research Center for the Emergency Drug, Beijing Institute of Pharmacology and Toxicology, Beijing, China.
  • Zhou P; National Engineering Research Center for the Emergency Drug, Beijing Institute of Pharmacology and Toxicology, Beijing, China.
  • Lv X; College of Otolaryngology Head and Neck Surgery, Chinese PLA General Hospital, Beijing, China.
  • Cui T; National Clinical Research Center for Otolaryngologic Diseases, Beijing, China.
  • Qiao Y; Key Lab of Hearing Science, Ministry of Education, Beijing, China.
  • Zhao H; Beijing Key Lab of Hearing Impairment for Prevention and Treatment, Beijing, China.
  • Guo W; College of Otolaryngology Head and Neck Surgery, Chinese PLA General Hospital, Beijing, China.
  • Chen W; National Clinical Research Center for Otolaryngologic Diseases, Beijing, China.
  • Li S; Key Lab of Hearing Science, Ministry of Education, Beijing, China.
  • Zhong W; Beijing Key Lab of Hearing Impairment for Prevention and Treatment, Beijing, China.
  • Lin J; 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, Chi
  • Yang S; National Engineering Research Center for the Emergency Drug, Beijing Institute of Pharmacology and Toxicology, Beijing, China.
Signal Transduct Target Ther ; 7(1): 175, 2022 06 10.
Article in En | MEDLINE | ID: mdl-35680846
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.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Hearing Loss / Ear, Inner Type of study: Prognostic_studies Limits: Humans Language: En Year: 2022 Type: Article

Full text: 1 Database: MEDLINE Main subject: Hearing Loss / Ear, Inner Type of study: Prognostic_studies Limits: Humans Language: En Year: 2022 Type: Article