Suppr超能文献

脂质体表面与人血红蛋白缀合,靶向递送至巨噬细胞。

Liposomes surface conjugated with human hemoglobin target delivery to macrophages.

机构信息

William G. Lowrie Department of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, Ohio 43210, USA.

出版信息

Biotechnol Bioeng. 2012 Mar;109(3):823-9. doi: 10.1002/bit.24340. Epub 2011 Nov 6.

Abstract

Current strategies to deliver therapeutic molecules to specific cell and tissue types rely on conjugation of antibodies and other targeting ligands directly to the therapeutic molecule itself or its carrier. This work describes a novel strategy to deliver therapeutic molecules into macrophages that takes advantage of the native hemoglobin (Hb) scavenging activity of plasma haptoglobin (Hp) and the subsequent uptake of the Hb-Hp complex into macrophages via CD163 receptor-mediated endocytosis. The drug delivery system described in this work consists of Hb decorated liposomes that can encapsulate any therapeutic molecule of interest, in this case the model fluorescent dye calcein was used in this study. The results of this study clearly demonstrate that this delivery system is specific towards macrophages and demonstrates the feasibility of using this approach in targeted drug delivery.

摘要

目前将治疗分子递送到特定细胞和组织类型的策略依赖于将抗体和其他靶向配体直接缀合到治疗分子本身或其载体上。本工作描述了一种将治疗分子递送到巨噬细胞中的新策略,该策略利用了血浆触珠蛋白(Hp)对天然血红蛋白(Hb)的清除活性,以及随后通过 CD163 受体介导的内吞作用将 Hb-Hp 复合物摄取到巨噬细胞中。本工作中描述的药物递送系统由 Hb 修饰的脂质体组成,该脂质体可以包封任何感兴趣的治疗分子,在本研究中使用了模型荧光染料 calcein。本研究的结果清楚地表明,该递药系统对巨噬细胞具有特异性,并证明了在靶向药物递送中使用这种方法的可行性。

相似文献

1
Liposomes surface conjugated with human hemoglobin target delivery to macrophages.
Biotechnol Bioeng. 2012 Mar;109(3):823-9. doi: 10.1002/bit.24340. Epub 2011 Nov 6.
2
Efficient intracellular drug-targeting of macrophages using stealth liposomes directed to the hemoglobin scavenger receptor CD163.
J Control Release. 2012 May 30;160(1):72-80. doi: 10.1016/j.jconrel.2012.01.034. Epub 2012 Jan 27.
4
Soluble macrophage-derived CD163: a homogenous ectodomain protein with a dissociable haptoglobin-hemoglobin binding.
Immunobiology. 2010 May;215(5):406-12. doi: 10.1016/j.imbio.2009.05.003. Epub 2009 Jul 5.
5
CD163 is the macrophage scavenger receptor for native and chemically modified hemoglobins in the absence of haptoglobin.
Blood. 2006 Jan 1;107(1):373-80. doi: 10.1182/blood-2005-03-1014. Epub 2005 Sep 27.
6
CD163: a signal receptor scavenging haptoglobin-hemoglobin complexes from plasma.
Int J Biochem Cell Biol. 2002 Apr;34(4):309-14. doi: 10.1016/s1357-2725(01)00144-3.
7
A novel process for transcellular hemoglobin transport from macrophages to cancer cells.
Cell Commun Signal. 2024 Nov 27;22(1):570. doi: 10.1186/s12964-024-01929-8.
9
Genetically determined heterogeneity in hemoglobin scavenging and susceptibility to diabetic cardiovascular disease.
Circ Res. 2003 Jun 13;92(11):1193-200. doi: 10.1161/01.RES.0000076889.23082.F1. Epub 2003 May 15.
10
Plasma clearance of hemoglobin and haptoglobin in mice and effect of CD163 gene targeting disruption.
Antioxid Redox Signal. 2013 Jun 10;18(17):2254-63. doi: 10.1089/ars.2012.4605. Epub 2012 Aug 29.

引用本文的文献

2
Tumor-Associated Macrophage Targeting of Nanomedicines in Cancer Therapy.
Pharmaceutics. 2023 Dec 29;16(1):61. doi: 10.3390/pharmaceutics16010061.
3
The Role of Tumor Epithelial-Mesenchymal Transition and Macrophage Crosstalk in Cancer Progression.
Curr Osteoporos Rep. 2023 Apr;21(2):117-127. doi: 10.1007/s11914-023-00780-z. Epub 2023 Feb 27.
4
Role and Mechanisms of Tumor-Associated Macrophages in Hematological Malignancies.
Front Oncol. 2022 Jul 7;12:933666. doi: 10.3389/fonc.2022.933666. eCollection 2022.
5
Full-length in meso structure and mechanism of rat kynurenine 3-monooxygenase inhibition.
Commun Biol. 2021 Feb 4;4(1):159. doi: 10.1038/s42003-021-01666-5.
6
Harnessing molecular recognition for localized drug delivery.
Adv Drug Deliv Rev. 2021 Mar;170:238-260. doi: 10.1016/j.addr.2021.01.008. Epub 2021 Jan 20.
7
Discovery of a sugar-based nanoparticle universally existing in boiling herbal water extracts and their immunostimulant effect.
Biochem Biophys Rep. 2018 Oct 11;16:62-68. doi: 10.1016/j.bbrep.2018.08.004. eCollection 2018 Dec.
10
Potential Use of Biological Proteins for Liver Failure Therapy.
Pharmaceutics. 2015 Aug 31;7(3):255-74. doi: 10.3390/pharmaceutics7030255.

本文引用的文献

1
Development of a dichloroacetic acid-hemoglobin conjugate as a potential targeted anti-cancer therapeutic.
Biotechnol Bioeng. 2011 Jun;108(6):1413-20. doi: 10.1002/bit.23071. Epub 2011 Feb 18.
2
3
Reversible cell-specific drug delivery with aptamer-functionalized liposomes.
Angew Chem Int Ed Engl. 2009;48(35):6494-8. doi: 10.1002/anie.200901452.
5
Tangential flow filtration of hemoglobin.
Biotechnol Prog. 2009 Jan-Feb;25(1):189-99. doi: 10.1002/btpr.119.
7
Antibody-modified liposomes for cancer chemotherapy.
Expert Opin Drug Deliv. 2008 Sep;5(9):1003-25. doi: 10.1517/17425247.5.9.1003.
9
Nanocarriers as an emerging platform for cancer therapy.
Nat Nanotechnol. 2007 Dec;2(12):751-60. doi: 10.1038/nnano.2007.387.
10
Liposomal drug delivery systems: an update review.
Curr Drug Deliv. 2007 Oct;4(4):297-305. doi: 10.2174/156720107782151269.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验