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重组腺相关病毒血清型 6 有效地转导原代人黑素细胞。

Recombinant adeno-associated virus serotype 6 efficiently transduces primary human melanocytes.

机构信息

School of Biological Sciences, University of Auckland, Auckland, New Zealand.

出版信息

PLoS One. 2013 Apr 30;8(4):e62753. doi: 10.1371/journal.pone.0062753. Print 2013.

DOI:10.1371/journal.pone.0062753
PMID:23646140
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3640030/
Abstract

The study of melanocyte biology is important to understand their role in health and disease. However, current methods of gene transfer into melanocytes are limited by safety or efficacy. Recombinant adeno-associated virus (rAAV) has been extensively investigated as a gene therapy vector, is safe and is associated with persistent transgene expression without genome integration. There are twelve serotypes and many capsid variants of rAAV. However, a comparative study to determine which rAAV is most efficient at transducing primary human melanocytes has not been conducted. We therefore sought to determine the optimum rAAV variant for use in the in vitro transduction of primary human melanocytes, which could also be informative to future in vivo studies. We have screened eight variants of rAAV for their ability to transduce primary human melanocytes and identified rAAV6 as the optimal serotype, transducing 7-78% of cells. No increase in transduction was seen with rAAV6 tyrosine capsid mutants. The number of cells expressing the transgene peaked at 6-12 days post-infection, and transduced cells were still detectable at day 28. Therefore rAAV6 should be considered as a non-integrating vector for the transduction of primary human melanocytes.

摘要

黑素细胞生物学的研究对于了解其在健康和疾病中的作用很重要。然而,目前将基因转移到黑素细胞的方法受到安全性或疗效的限制。重组腺相关病毒(rAAV)已被广泛研究作为基因治疗载体,具有安全性,并与无基因组整合的持续转基因表达相关。rAAV 有 12 种血清型和许多衣壳变体。然而,尚未进行哪种 rAAV 最有效地转导原代人黑素细胞的比较研究。因此,我们试图确定最适合用于体外转导原代人黑素细胞的 rAAV 变体,这也可能对未来的体内研究提供信息。我们筛选了 8 种 rAAV 变体来转导原代人黑素细胞,并确定 rAAV6 是最佳的血清型,可转导 7-78%的细胞。rAAV6 酪氨酸衣壳突变体的转导没有增加。感染后 6-12 天达到转基因表达细胞的峰值,感染后 28 天仍可检测到转导细胞。因此,rAAV6 应被视为非整合载体,用于转导原代人黑素细胞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b95d/3640030/e24ecb348f22/pone.0062753.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b95d/3640030/5ac9437b7bd0/pone.0062753.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b95d/3640030/9bbcd9cd622d/pone.0062753.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b95d/3640030/e24ecb348f22/pone.0062753.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b95d/3640030/5ac9437b7bd0/pone.0062753.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b95d/3640030/9bbcd9cd622d/pone.0062753.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b95d/3640030/e24ecb348f22/pone.0062753.g004.jpg

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2
From genes to drugs: targeted strategies for melanoma.从基因到药物:黑色素瘤的靶向治疗策略。
Nat Rev Cancer. 2012 Apr 5;12(5):349-61. doi: 10.1038/nrc3218.
3
Differentiated melanocyte cell division occurs in vivo and is promoted by mutations in Mitf.有丝分裂后黑素细胞在体内发生分裂,其由 Mitf 突变所促进。
Development. 2011 Aug;138(16):3579-89. doi: 10.1242/dev.064014. Epub 2011 Jul 19.
4
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5
Structural characterization of the dual glycan binding adeno-associated virus serotype 6.六型腺相关病毒双重糖基结合结构特征。
J Virol. 2010 Dec;84(24):12945-57. doi: 10.1128/JVI.01235-10. Epub 2010 Sep 22.
6
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