このコンテンツを視聴するには、JoVE 購読が必要です。 サインイン又は無料トライアルを申し込む。
This protocol is based on LPS and ATP-induced death of PMA-differentiated THP-1 macrophages. We use flow cytometry to analyze Annexin V and 7-AAD double staining to detect cell death, using the whole cell and employing scanning electron microscopy to observe the cell membrane morphology.
Cell death is a fundamental process in all living organisms. The protocol establishes a lipopolysaccharide (LPS) and adenosine triphosphate (ATP)-induced phorbol-12-myristate-13-acetate (PMA)-differentiated lipid deposition in human monocyte (THP-1) macrophage model to observe cell death. LPS combined with ATP is a classic inflammatory induction method, often used to study pyroptosis, but apoptosis and necroptosis also respond to stimulation by LPS/ATP. Under normal circumstances, phosphatidylserine is only localized in the inner leaflet of the plasma membrane. However, in the early stages of pyroptosis, apoptosis, and necroptosis, the cell membrane remains intact and exposed to phosphatidylserine, and in the later stages, the cell membrane loses its integrity. Here, flow cytometry was used to analyze Annexin V and 7-Aminoactinomycin D (AAD) double staining to detect the cell death from the whole cells. The results show that substantial cells died after stimulation with LPS/ATP. Using scanning electron microscopy, we observe the possible forms of cell death in individual cells. The results indicate that cells may undergo pyroptosis, apoptosis, or necroptosis after stimulation with LPS/ATP. This protocol focuses on observing the death of macrophages after stimulation with LPS/ATP. The results showed that cell death after LPS and ATP stimulation is not limited to pyroptosis and that apoptosis and necrotic apoptosis can also occur, helping researchers better understand cell death after LPS and ATP stimulation and choose a better experimental method.
Cell death is a fundamental physiological process in all living organisms. In recent years, substantial studies have shown that cell death is involved in the immunity and balance within the organism. Studying cell death helps us better understand the onset and development of diseases. Several forms of programmed cell death have been described, and some key targets in these processes have been identified. Pyroptosis, apoptosis, and necroptosis are the three genetically defined programmed cell death pathways involved in internal balance and disease1.
Pyroptosis is characterized by the formation of membrane pores and th....
1. Cell line and cell culture
The cell samples were treated as described in the protocol and flow cytometry detection was done. Normal cells cannot be stained with Annexin V and 7-AAD (Annexin V-/7-AAD-). In the early stages of pyroptosis, apoptosis, and necroptosis, PS was exposed and bound to Annexin V, but the cell membrane was still intact and excluded 7-AAD from the extracellular space (Annexin V+/7-AAD-). In the later stages, the cell membrane loses its integrity, cells are simultaneously stained by Annexin V and 7-AAD, showing double positive .......
In this manuscript, two methods were used to detect LPS and ATP-induced death of PMA-differentiated THP-1 macrophages. Annexin V/7-AAD double staining was used, and the results were analyzed by flow cytometry from overall staining. As with other flow cytometric analysis, a group of unstained cells and two groups of single-stained cells were set up to exclude false positive and false negative results. The results show that after LPS/ATP stimulation, several cells lost membrane integrity, indicating that cell death may hav.......
We express our great appreciation to Jiayi Sun and Lu Yang at Innovative Institute of Chinese Medicine and Pharmacy, Chengdu University of Traditional Chinese Medicine, for the assistance with flow cytometry, Cuiping Chen at State Key Laboratory of Southwestern Chinese Medicine Resources, for the help with scanning electron microscopy. This work was supported by the National Natural Science Foundation of China [82104491], the Natural Science Foundation of Sichuan [2023NSFSC0674], and the Post-doctoral Science Foundation of China [2021M693789].
....Name | Company | Catalog Number | Comments |
0.25% pancreatic enzyme solution (excluding EDTA) | BOSTER Biological Technology co.ltd | PYG0068 | |
5 mL Polystyrene Round-Bottom Tube | CORNING | 352235 | |
5 mL centrifuge tube | Labgic Technology Co., Ltd. | BS-50-M | |
6-well plate | Sorfa Life Science Research Co.,Ltd | 220100 | |
Annexin V-PE/7-AAD apoptosis analysis kit | Absin (Shanghai) Biological Technology co.ltd | abs50007 | Annexin V-PE, 7-AAD, 5×Binding buffer, Apoptosis Positive Control Solution |
celculture CO2 incubator | Esco (Shanghai) Enterprise Development Co., Ltd. | N/A | |
cell culture dish, 100 mm | Sorfa Life Science Research Co.,Ltd | 230301 | |
Cellometer K2 Fluorescent Cell Counter | Nexcelom Bioscience LLC | Cellometer K2 | |
Cellometer SD100 Counting Chambers | Nexcelom Bioscience LLC | CHT4-SD100-002 | |
centrifuge machine | Hunan Xiangyi Laboratory Instrument Development Co., Ltd | L530 | |
chromium alum | Guangdong Wengjiang Chemical Reagent Co., Ltd. | PA04354 | |
cover glasses, 9 mm | Labgic Technology Co., Ltd. | BS-09-RC | |
critical point dryer | Quorum Technologies | K850 | |
dimethyl sulfoxide | BOSTER Biological Technology co.ltd | PYG0040 | |
electron microscope fixative | Servicebio Technology co.ltd | G1102 | 2.5% glutaric dialdehyde, 100 mM phosphorous salts |
electronic balance | SHIMADZU | ATX124 | |
ethanol absolute | Chengdu Kelong Chemical Co., Ltd | 2021033102 | |
flow cytometer | Becton,Dickinson and Company | FACSCanto | |
flow cytometry analysis software | Becton,Dickinson and Company | BD FACSDivaTM Software | |
gelatin | Guangdong Wengjiang Chemical Reagent Co., Ltd. | PA00256 | |
High resolution cold field emission scanning electron microscope | TITACHI | Regulus 8100 | |
human monocytic cell line THP-1 | Procell Life Science&Technology Co.,Ltd. | CL0233 | |
inverted microscope | Leica Microsystems Co., Ltd | DMi1 | |
IR Vortex Mixer | VELP Scientifica Srl | ZX4 | |
lipopolysaccharide | Beijing Solarbio Science & Technology Co.,Ltd. | L8880 | LPS is derived from Escherichia coli 055:B5 |
Na2ATP | Beijing Solarbio Science & Technology Co.,Ltd. | A8270 | |
phorbol-12-myristate-13-acetate | Beijing Solarbio Science & Technology Co.,Ltd. | P6741 | |
phosphate-buffered saline | Servicebio Technology co.ltd | G4202 | |
Pipette | Eppendorf AG | N/A | |
pipette tips, 10 μL | Servicebio Technology co.ltd | T-10PL | |
pipette tips, 1 mL | Servicebio Technology co.ltd | T-1250L | |
pipette tips, 200 μL | Servicebio Technology co.ltd | T-200L | |
RPMI-1640 complete culture media | Procell Life Science&Technology Co.,Ltd. | CM0233 | RPMI-1640 + 10% FBS + 0.05mM β-mercaptoethanol + 1% P/S |
RPMI-1640 culture media | Shanghai BasalMedia Technologies Co., LTD. | K211104 | |
sheath fluid | BECKMAN COULTER | 8546733 | |
sputter coater | Cressington Scientific Instruments Ltd | 108 | |
thermostatic water bath | GUOHUA Electric Appliance CO.,Ltd | HH-1 |
This article has been published
Video Coming Soon
JoVEについて
Copyright © 2023 MyJoVE Corporation. All rights reserved