创伤性脑损伤
基因沉默
医学
体内
药理学
肽
小胶质细胞
药物输送
化学
炎症
免疫学
生物
基因
生物化学
生物技术
有机化学
精神科
作者
Aman P. Mann,Pablo Scodeller,Sazid Hussain,Jinmyoung Joo,Ester J. Kwon,Gary B. Braun,Tarmo Mölder,Zhi Gang She,Venkata Ramana Kotamraju,Barbara Ranscht,Stan Krajewski,Tambet Teesalu,Sangeeta N. Bhatia,Michael J. Sailor,Erkki Ruoslahti
摘要
Traumatic brain injury (TBI) is a major health and socio-economic problem, but no pharmacological agent is currently approved for the treatment of acute TBI. Thus, there is a great need for advances in this field. Here, we describe a short peptide (sequence CAQK) identified by in vivo phage display screening in mice with acute brain injury. The CAQK peptide selectively binds to injured mouse and human brain, and systemically injected CAQK specifically homes to sites of brain injury in mouse models. The CAQK target is a proteoglycan complex upregulated in brain injuries. Coupling to CAQK increased injury site accumulation of systemically administered molecules ranging from a drug-sized molecule to nanoparticles. CAQK-coated nanoparticles containing silencing oligonucleotides provided the first evidence of gene silencing in injured brain parenchyma by systemically administered siRNA. These findings present an effective targeting strategy for the delivery of therapeutics in clinical management of acute brain injuries.
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