[1]郑晓丹,王 婷,胡玉海.改良组织贴壁法分离培养新生乳小鼠原代肺成纤维细胞的研究[J].现代检验医学杂志,2024,39(06):206-210.[doi:10.3969/j.issn.1671-7414.2024.06.036]
 ZHENG Xiaodan,WANG Ting,HU Yuhai.Study on Isolation and Culture of Primary Lung Fibroblasts from Newborn Mice by Improved Tissue Adhesion Method[J].Journal of Modern Laboratory Medicine,2024,39(06):206-210.[doi:10.3969/j.issn.1671-7414.2024.06.036]
点击复制

改良组织贴壁法分离培养新生乳小鼠原代肺成纤维细胞的研究()
分享到:

《现代检验医学杂志》[ISSN:/CN:]

卷:
第39卷
期数:
2024年06期
页码:
206-210
栏目:
论著
出版日期:
2024-11-15

文章信息/Info

Title:
Study on Isolation and Culture of Primary Lung Fibroblasts from Newborn Mice by Improved Tissue Adhesion Method
文章编号:
1671-7414(2024)06-206-05
作者:
郑晓丹王 婷胡玉海
(武汉市汉口医院检验科,武汉 430010)
Author(s):
ZHENG Xiaodan WANG Ting HU Yuhai
(Department of Clinical Laboratory, Wuhan Hankou Hospital, Wuhan 430010,China)
关键词:
肺成纤维细胞原代培养组织贴壁法流式细胞染色
分类号:
R-332
DOI:
10.3969/j.issn.1671-7414.2024.06.036
文献标志码:
A
摘要:
目的 建立改良版简单高效的原代小鼠肺成纤维细胞(lung fibroblast,LFB)分离培养方案,研究其体外生长特性。方法 无菌条件下,分别取3 天龄小鼠和8 周龄小鼠肺组织,剪成1mm3 大小,分别采用含10g/dl 胎牛血清(fetalbovine serum,FBS)和20g/dl 胎牛血清的高糖DMEM 培养液进行组织贴壁法培养。采用差时贴壁法对LFB 进行纯化,倒置显微镜下动态观察细胞生长状态及贴壁状态,采用流式细胞特异性分子染色法对LFB 进行鉴定,传代培养后的第3 代细胞采用CCK-8(cell counting kit-8)法检测细胞活性。结果 3 天龄小鼠在20g/dl FBS 浓度条件下采用改良组织贴壁法进行培养,培养后第2 天开始向周边呈放射状长出细胞,第7 天细胞生长密度达90 %,细胞形态呈长梭形。经差时贴壁法纯化后,CD140a 阳性且CD45 阴性细胞占比可达90% 以上,连续传代3 次后保持较好细胞活性。结论 改良的组织贴壁法可简单高效地获得大量纯化的、活性好的小鼠LFB,为肺部炎症、肿瘤及药物体外疗效等研究奠定基础。
Abstract:
Objective To establish an improved simple and efficient method for isolation and culture of primary lung fibroblasts (LFB) from neonatal mice, and study their growth characteristics in vitro. Methods The lungs of 3-days-old mice or 8-weeksold mice were taken under sterile conditions, and the stromal tissue was cut into 1mm3 tissue mass. High-glucose DMEM culture medium containing 10g/dl fetal bovine serum (FBS) or 20g/dl FBS was used for tissue adhesion culture. The LFB was purified by the differential time adhesion method, and the growth morphology and adherence state of the cells were observed dynamically under an inverted microscope. The primary LFB was identified by flow cytometry. The activity of the third-generation cell after culture was detected by CCK-8 assay. Results Lung tissues in mice at 3 days of age and 20g/dl FBS concentration cultured by the improved tissue mass adherent cultured method began to grow radially to the periphery on the 2nd day. On the day 7th, the cells growth density reached 90%, and the cell morphology was as a spindle. The CD140a positive and CD45 negative cells reached more than 90% after purification by differential time adhesion method, and the cells still maintain good cell activity after cultured for 3 generations. Conclusion The improved tissue adhesion method can obtain a large number of purified mice LFB with good activity simply and efficiently, which lays a foundation for the study of lung inflammation, tumors and in vitro efficacy of drugs.

参考文献/References:

[1] YUAN Jihong, MA Yu, YUAN Linghong, et al. Baicalein attenuates bleomycin-induced lung fibroblast senescence and lung fibrosis through restoration of Sirt3 expression[J]. Pharmaceutical Biology, 2023, 61(1): 288-297.
[2] LIU Xue, GENG Yan, LIANG Jiurong, et al. HER2 drives lung fibrosis by activating a metastatic cancer signature in invasive lung fibroblasts[J]. Journal of Experimental Medicine, 2022, 219(10): e20220126.
[3] MAZUMDAR A, URDINEZ J, BORO A, et al. Osteosarcoma-derived extracellular vesicles induce lung fibroblast reprogramming [J]. International Journal of Molecular Sciences, 2020, 21(15): 5451.
[4] HUANG Guanling, LIANG Jiurong, HUANG Kevin,et al. Basal cell-derived WNT7A promotes fibrogenesis at the fibrotic niche in idiopathic pulmonary fibrosis [J]. American Journal of Respiratory Cell and Molecular Biology, 2023, 68(3): 302-313.
[5] 王志超, 武琦, 冯凡超, 等.改良组织法高效分离纯化成年小鼠肺成纤维细胞[J].中华中医药学刊,2018, 36(12): 2842-2844, 后插2- 后插3. WANG Zhichao, WU Qi, FENG Fanchao, et al. Isolation and purification of adult mouse lung fibroblasts by efficient and modified tissue method[J]. Chinese Archives of Traditional Chinese Medicine,2018, 36(12): 2842-2844, F0002-F0003.
[6] ABADE DOS SANTOS F A, CARVALHO C L, ALMEIDA I, et al. Simple method for establishing primary leporidae skin fibroblast cultures[J]. Cells, 2021, 10(8): 2100.
[7] TAJIMA K, OKADA M, KUDO R, et al. Primary cell culture of canine corneal endothelial cells [J]. Veterinary Ophthalmology, 2021, 24(5): 447-454.
[8] CAVAGNERO K J, GALLO R L. Essential immune functions of fibroblasts in innate host defense [J]. Frontiers in Immunology, 2022, 13: 1058862.
[9] GROUT J A, SIRVEN P, LEADER A M, et al. Spatial positioning and matrix programs of cancer-associated fibroblasts promote T-cell exclusion in human lung tumors[J]. Cancer Discovery, 2022, 12(11): 2606-2625.
[10] GONG Zheng, LI Qing, SHI Jiayuan, et al. Lung fibroblasts facilitate pre-metastatic niche formation by remodeling the local immune microenvironment[J]. Immunity, 2022, 55(8): 1483-1500, e9.
[11] PHOGAT S, THIAM F, AL YAZEEDI S, et al. 3D in vitro hydrogel models to study the human lung extracellular matrix and fibroblast function[J]. Respiratory Research, 2023, 24(1): 242.
[12] CHARNI-NATAN M, GOLDSTEIN I. Protocol for primary mouse hepatocyte isolation [J]. STAR Protocols, 2020, 1(2): 100086.
[13] 刘先宁, 汪耀, 朱秀萍, 等.人角膜基质间充质干细胞的分离培养及表型鉴定[J].现代检验医学杂志,2019, 34(4): 28-30, 34. LIU Xianning, WANG Yao, ZHU Xiuping, et al. Isolation,culture and phenotype identification of human corneal stromal mesenchymal stem cells[J]. Journal of Modern Laboratory Medicine, 2019, 34(4): 28-30, 34.
[14] PATEL B B, CLARK K L, KOZIK E M, et al. Isolation and culture of primary embryonic zebrafish neural tissue [J]. Journal of Neuroscience Methods, 2019, 328: 108419.
[15] VALYI-NAGY K, BETSOU F, SUSMA A, et al. Optimization of viable glioblastoma cryopreservation for establishment of primary tumor cell cultures[J]. Biopreservation and Biobanking, 2021, 19(1): 60-66.
[16] EHLEN L, ARNDT J, TREUE D, et al. Novel methods for in vitro modeling of pancreatic cancer reveal important aspects for successful primary cell culture[J]. BMC Cancer, 2020, 20(1): 417.
[17] 刘姿麟, 林慕之, 况春燕, 等. 大鼠主动脉血管平滑肌细胞原代培养与鉴定[J].贵州医科大学学报,2017, 42(2): 125-129. LIU Zilin, LIN Muzhi, KUANG Chunyan, et al. Culture and identification of primary generation of vascular smooth muscle cell of rat[J]. Journal of Guizhou Medical University, 2017, 42(2): 125-129.
[18] 钱凯, 唐琳俊, 王希, 等. 新生大鼠原代小胶质细胞分离培养方法的改良[J].临床神经外科杂志, 2019,16(1): 1-5. QIAN Kai, TANG Linjun, WANG Xi, et al. Modified method for cultivating primary microglia of neonatal rat[J]. Journal of Clinical Neurosurgery, 2019, 16(1): 1-5.

备注/Memo

备注/Memo:
基金项目:武汉市卫健委中医药科研项目面上项目(立项编号:WZ24A25)。
作者简介:郑晓丹(1990-),女,硕士,主管技师,研究方向:肿瘤免疫,E-mail:283350862@qq.com。
通讯作者:胡玉海(1975-),女,本科,主任技师,研究方向:免疫学检验,E-mail:xyz27315@126.com。
更新日期/Last Update: 2024-11-15