Original Article
Quantitative analysis of autophagy in green fluorescent protein-light chain 3 transgenic murine keratinocytes
Tingting Jin, Heidemarie Rossiter, Michael Mildner, Florian Gruber, Leopold Eckhart, Erwin Tschachler, Yi Zhao
Published 2018-03-15
Cite as Chin J Dermatol, 2018, 51(3): 182-185. DOI: 10.3760/cma.j.issn.0412-4030.2018.03.004
Abstract
ObjectiveTo explore a high-throughput method for quantitative analysis of autophago-somes.
MethodsGreen fluorescent protein-light chain 3 (GFP-LC3) transgenic murine keratinocytes were randomly divided into 4 groups: control group receiving no treatment, starvation group subjected to starved culture, 20 J/cm2 ultraviolet A (UVA) group treated with 20 J/cm2 UVA radiation, and 40 J/cm2 UVA group treated with 40 J/cm2 UVA radiation. After 6-hour treatment, the cells were fixed, and images were acquired by confocal laser scanning microscopy. A macro was created by the ImageJ software to automatically quantify the GFP-LC3 puncta in the cells and the number of cells. Then, the level of autophagy was compared among different groups.
ResultsBy using the macro created by the ImageJ software, autophago-somes in the keratinocytes were successfully identified and quantified. Less than 0.6 second was needed for analyzing an image of 4.2 mega pixels in a test computer. The average number of autophagosomes in keratinocytes was significantly higher in the starvation group, 20-J/cm2 UVA group and 40-J/cm2 UVA group than in the control group whether with the treatment with pepstatin A (F = 20.05, P <0.05) or not (F = 5.01, P < 0.05) . This method could successfully differentiate the autophagy levels among the starvation group, UVA irradiation groups and control group.
ConclusionA new high-throughput method, which can rapidly and accurately quantify GFP-LC3 puncta in cells, is established successfully to quantificationally detect autophagy.
Key words:
Autophagy; Keratinocytes; Green fluorescent proteins; Microscopy, confocal; Image processing, computer-assisted
Contributor Information
Tingting Jin
Department of Dermatology and Venereology, Peking University First Hospital, Beijing 100034, China (the current affiliation: Plastic and Reconstructive Surgery, Zhejiang Provincial People′s Hospital, Hangzhou 310014, China)
Heidemarie Rossiter
Research Department of Biology and Pathobiology of the Skin, Medical University of Vienna, Vienna 1090, Austria
Michael Mildner
Research Department of Biology and Pathobiology of the Skin, Medical University of Vienna, Vienna 1090, Austria
Florian Gruber
Research Department of Biology and Pathobiology of the Skin, Medical University of Vienna, Vienna 1090, Austria
Leopold Eckhart
Research Department of Biology and Pathobiology of the Skin, Medical University of Vienna, Vienna 1090, Austria
Erwin Tschachler
Research Department of Biology and Pathobiology of the Skin, Medical University of Vienna, Vienna 1090, Austria
Yi Zhao
Department of Dermatology, Beijing Tsinghua Changgung Hospital, Affiliated to Tsinghua University, Beijing 102218, China
