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利用 CRISPR/Cas9 基因组编辑系统从小鼠颌下腺生产功能性人神经生长因子。

Production of functional human nerve growth factor from the submandibular glands of mice using a CRISPR/Cas9 genome editing system.

机构信息

CAS Key Laboratory of Biobased Materials, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, No. 189 Songling Road, Qingdao, 266101, China.

University of Chinese Academy of Sciences, No. 19(A) Yuquan Road, Beijing, 100049, China.

出版信息

World J Microbiol Biotechnol. 2020 Oct 26;36(12):176. doi: 10.1007/s11274-020-02951-x.

Abstract

Nerve growth factor (NGF) is an essential trophic factor for the growth and survival of neurons in the central and peripheral nervous systems. For many years, mouse NGF (mNGF) has been used to treat various neuronal and non-neuronal disorders. However, the biological activity of human NGF (hNGF) is significantly higher than that of mNGF in human cells. Using the CRISPR/Cas9 system, we constructed the transgenic mice expressing hNGF specifically in their submandibular glands. As demonstrated by fluorescence immunohistochemical staining, these mice produced hNGF successfully, with 0.8 mg produced per gram of submandibular glands. hNGF with 99% purity was successfully extracted by two-step ion-exchange chromatography and one-step size-exclusion chromatography from the submandibular glands of these transgenic mice. Further, the purified hNGF was verified by LC-MS/MS. We analyzed the NH-terminus of hNGF using both Edman degradation and LC-MS/MS-based methods. Both results showed that the obtained hNGF lost the NH-terminal octapeptide (SSSHPIFH). Moreover, the produced hNGF demonstrated a strong promotion in the proliferation of TF1 cells.

摘要

神经生长因子(NGF)是中枢和周围神经系统中神经元生长和存活所必需的营养因子。多年来,小鼠 NGF(mNGF)一直被用于治疗各种神经元和非神经元疾病。然而,在人类细胞中,人 NGF(hNGF)的生物学活性明显高于 mNGF。我们使用 CRISPR/Cas9 系统构建了在颌下腺特异性表达 hNGF 的转基因小鼠。荧光免疫组织化学染色显示,这些小鼠成功产生了 hNGF,每克颌下腺产生 0.8 毫克 hNGF。通过两步离子交换层析和一步分子筛层析从这些转基因小鼠的颌下腺中成功提取出纯度为 99%的 hNGF。进一步通过 LC-MS/MS 对纯化的 hNGF 进行了验证。我们使用 Edman 降解和基于 LC-MS/MS 的方法分析了 hNGF 的 NH 末端。两种结果均表明,得到的 hNGF 失去了 NH 末端的八肽(SSSHPIFH)。此外,产生的 hNGF 强烈促进了 TF1 细胞的增殖。

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