用荧光图像示踪不同分化的食管癌细胞Cx43的空间分布
[1] DE BRABANDER M, NUYDENS R, GEERTS H, et al. Dynamic behavior of the transferrin receptor followed in living epidermoid carcinoma (A431)cells with nanovid microscopy[J]. Cell Motility and the Cytoskeleton, 1988, 9(1): 30-47.
[2] CHENOUARD N, SMAL I, DE CHAUMONT F, et al. Objective comparison of particle tracking methods [J]. Nature Methods, 2014, 11(3): 281-289.
[3] MANZO C, GARCIA-PARAJO M F. A review of progress in single particle tracking: from methods to biophysical insights[J]. Reports on Progress in Physics, 2015, 78(12): 124601.
[4] CHEN X, LEE K, REN X, et al. Synthesis of a highly HOCl-selective fluorescent probe and its use for imaging HOCl in cells and organisms[J]. Nature Protocols, 2016, 11(7): 1219-1228.
[5] HUANG B, BATES M, ZHUANG X. Super-resolution fluorescence microscopy[J]. Annual Review of Biochemistry, 2009, 78: 993-1016.
[6] PATTERSON G, DAVIDSON M, MANLEY S, et al. Superresolution imaging using single-molecule localization[J]. Annual Review of Physical Chemistry, 2010, 61: 345-367.
[7] GIEPMANS B N G, ADAMS S R, ELLISMAN M H, et al. The fluorescent toolbox for assessing protein location and function[J]. Science, 2006, 312 (5771): 217-224.
[8] WELCH C M, ELLITT H, DANUSER G, et al. Imaging the coordination of multiple signaling activities in living cells[J]. Nature Reviews Molecular Cell Biology, 2011, 12(11): 749-756.
[9] SZYMANSKI C J, HUMPHRIES W H, PAYNE C K. Single particle tracking as a method to resolve differences in highly colocalized proteins[J]. Analyst, 2011, 136(17): 3527-3533.
[10] BONACQUISTI E E, NGUYEN J. Connexin 43 (Cx43)in cancer: implications for therapeutic approaches via gap junctions[J].Cancer Letters, 2019, 442: 439-444.
[11] FAN S Q, ZHOU M, XIANG Q, et al. In situ expression of connexins in various carcinomas[J]. Chinese Journal of Cancer, 2003, 22(7): 686-690.
[12] 王光宇. 食管鳞癌组织中连接蛋白43表达的临床意义[D]. 北京: 解放军医学院, 2014: 1-39.
WANG guangyu. The expression of Cx43 protein in esophageal squamous cell carcinoma tissues and its clinical significance[D]. Beijing: PLA Medical College, 2014: 1-39.
[13] ALCOR D, GOUZER G, TRILLER A. Single-particle tracking methods for the study of membrane receptors dynamics[J]. European Journal of Neuroscience, 2009, 30(6): 987-997.
[14] CHENOUARD N, SMAL I, DE CHAUMONT F, et al. Objective comparison of particle tracking methods[J]. Nature Methods, 2014, 11(3): 281-289.
[15] JAQAMAN K, LOERKE D, METTLEN M, et al. Robust single-particle tracking in live-cell time-lapse sequences[J]. Nature Methods, 2008, 5(8): 695-702.
[16] YANG G. Bioimage informatics for understanding spatiotemporal dynamics of cellular processes[J]. Wiley Interdisciplinary Reviews: Systems Biology and Medicine, 2013, 5(3): 367-380.
[17] SEGURA R L, AGUILA-ARCOS S, UGARTE-URIBE B, et al. Subcellular location of the coupling protein TrwB and the role of its transmembrane domain[J]. Biochimica et Biophysica Acta, 2014, 1838(1): 223-230.
[18] FRANK D K, SZYMKOWIAK B, HUGHES C A. Connexin expression and gap junctional intercellular communication in human squamous cell carcinoma of the head and neck[J]. Otolaryngology-Head and Neck Surgery, 2006, 135(5): 736-743.
[19] SOLAN J L, HINGORANI S R, LAMPE P D. Changes in connexin43 expression and localization during pancreatic cancer progression[J]. Journal of Membrane Biology, 2012, 245(5-6): 255-262.
[20] 林珏龙, 陈春桂, 沈志忠, 等。顺铂靶向食管癌细胞周期Cx43表达的研究[J]. 激光生物学报, 2017, 26(5): 432-437.
[21] HANNA E A, UMHAUER S, ROSHONG S L, et al. Gap junctional intercellular communication and connexin43 expression in human ovarian surface epithelial cells and ovarian carcinomas in vivo and in vitro[J]. Carcinogenesis, 1999, 20 (7): 1369-1373.
[22] KING T J, FUKUSHIMA L H, HIEBER A D, et al. Reduced levels of connexin43 in cervical dysplasia: inducible expression in a cervical carcinoma cell line decreases neoplastic potential with implications for tumor progression[J]. Carcinogenesis, 2000, 21(6): 1097-1109.
[23] ALLERSMA M W, WANG L, AXELROD D, et al. Visualization of regulated exocytosis with a granule-membrane probe using total internal reflection microscopy[J]. Molecular Biology of the Cell, 2004, 15(10): 4658-4668.
[24] HOLZ R W, AXELROD D. Secretory granule behaviour adjacent to the plasma membrane before and during exocytosis: total internal reflection fluorescence microscopy studies[J]. Acta Physiologica (Oxf), 2008, 192(2): 303-307.
[25] SICK B, HECHT B, NOVOTNY L. Orientational imaging of single molecules by annular illumination[J]. Physical Review Letters, 2000, 85(21): 4482-4485.
[26] MATSUNO A, MIZUTANI A, OKINAGA H, et al. Molecular morphology of pituitary cells, from conventional immunohistochemistry to fluorescein imaging[J]. Molecules, 2011, 16(5): 3618-3635.
[27] BARMAN B, BHATTACHARYYA S N. mRNA targeting to endoplasmic reticulum precedes ago protein interaction and microRNA (miRNA)-mediated translation repression in mammalian Cells[J]. Journal of Biological Chemistry, 2015, 290(41): 24650-24656.
林珏龙, 沈志忠, 刘柳, 庄冰蓉, 朴中贤, 李伟秋. 用荧光图像示踪不同分化的食管癌细胞Cx43的空间分布[J]. 激光生物学报, 2019, 28(5): 439. LIN Juelong, SHEN Zhizhong, LIU Liu, ZHUANG Bingrong, PIAO Zhongxian, LI Weiqiua. Tracking the Spatial Distribution of Cx43 in Different Differentiated Esophageal Cancer Cells Using Fluorescence Images[J]. Acta Laser Biology Sinica, 2019, 28(5): 439.