Isolation and identification of side population cells in human lung adenocarcinoma cell line A549.
- Author:
Tong XIE
1
;
Li LI
;
Dan-rong LI
;
Nai-quan MAO
;
De-seng LIU
;
Chuan-tian ZUO
;
Wei ZHANG
;
Ding-ming HUANG
Author Information
- Publication Type:Journal Article
- MeSH: ATP-Binding Cassette Transporters; metabolism; Adenocarcinoma; pathology; Animals; Cell Cycle; Cell Differentiation; Cell Line, Tumor; Cell Proliferation; drug effects; Cell Transformation, Neoplastic; metabolism; Fluorouracil; metabolism; Humans; Lung Neoplasms; pathology; Mice, Nude; Neoplasm Proteins; metabolism; Neoplasm Transplantation; Neoplastic Stem Cells; drug effects; Side-Population Cells
- From: Chinese Journal of Oncology 2011;33(2):84-90
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo isolate and characterize the side population cells (SP cells) in the lung adenocarcinomas cell line A549.
METHODSThe protein expression of ABCG2 in human lung adenocarcinoma cell line A549 was detected by immunohistochemistry. SP and NSP cells in the cell line A549 were isolated by FACS, and their differentiation was analysed. ABCG2 expression in the two cell subsets was detected by RT-PCR. The cell growth curves, cell division indexes, cell cycles, plate clone formation tests, migration and invasion assays, chemotherapeutic susceptibility tests, tests of the intracellular drug levels, and the tumor cell implantation experiments on nude mice were applied to study the biological properties of the two cell subsets. The expression of ABCG2 in the transplanted tumor in nude mice was detected by immunohistochemistry and RT-PCR.
RESULTSThe positive rate of ABCG2 expression in the A549 cells by immunohistochemistry was 2.13%. SP and NSP cells were isolated by FACS. The SP cells could produce both SP and NSP cells, while NSP cells only produced NSP cells. SP cells expressed ABCG2, but NSP cells did not. The proliferation and migration abilities of the two cell subsets were similar, but the invasion and tumorigenic ability of SP cells was significantly higher than that of NSP cells. The susceptibilities to DDP and its intracellular levels of the two cell subsets were similar, but the susceptibilities to 5-FU, VP16, NVB and GEM and their intracellular levels of NSP cells were significantly higher than those of the SP cells.
CONCLUSIONSSP cells in the human lung adenocarcinomas cell line A549 is enriched with tumor stem cells. An effective way to get lung adenocarcinomas stem cells is to isolate SP cells by FACS.