Department of Chemical Engineering, University of California, Santa Barbara, CA 93106, USA.
Proc Natl Acad Sci U S A. 2011 Sep 20;108(38):15816-21. doi: 10.1073/pnas.1016152108. Epub 2011 Sep 8.
Delivery of macromolecules into cells and tissues such as skin is a major challenge. This obstacle poses a particular challenge for the delivery of siRNA where cellular and tissue level transport barriers need to be overcome. siRNAs are potential therapeutics for various dermatological diseases including psoriasis, atopic dermatitis, and cancer; however, their utility is limited by their low absorption across the stratum corneum (SC) and into viable cells of skin. Here, we address this challenge using a peptide identified by phage display termed skin penetrating and cell entering (SPACE) peptide. In vitro studies indicated that the SPACE peptide, when conjugated to cargoes such as small molecules and proteins, was able to facilitate their penetration across the SC into epidermis and dermis. The peptide also exhibited increased penetration into various cells including keratinocytes, fibroblasts, and endothelial cells, likely through a macropinocytosis pathway. The ability of SPACE peptide to deliver siRNA was tested in vivo using two targets, interleukin-10 and GAPDH. Conjugation of the peptide to siRNA led to their enhanced absorption into skin and knockdown of corresponding protein targets.
将大分子递送到细胞和组织(如皮肤)是一项重大挑战。对于 siRNA 的递送来 说,这一障碍尤其具有挑战性,因为需要克服细胞和组织水平的运输障碍。siRNA 是治疗各种皮肤病的潜在疗法,包括银屑病、特应性皮炎和癌症;然而,由于它们在穿过角质层(SC)和进入皮肤的有活力的细胞方面吸收能力较低,其应用受到限制。在这里,我们使用一种通过噬菌体展示鉴定的肽来解决这一挑战,该肽称为穿透皮肤和进入细胞(SPACE)肽。体外研究表明,当 SPACE 肽与小分子和蛋白质等货物结合时,能够促进它们穿过 SC 进入表皮和真皮。该肽还表现出对各种细胞(包括角质形成细胞、成纤维细胞和内皮细胞)的穿透增加,可能是通过巨胞饮途径。SPACE 肽递送 siRNA 的能力在体内使用两种靶标(白细胞介素-10 和 GAPDH)进行了测试。将肽与 siRNA 缀合导致其增强吸收到皮肤中,并降低相应的蛋白靶标。