[Biological characteristics of human peripheric CD4+ CD25- T cells isolated and cultured in vitro].
Miao‐Shang Su, Manhuan Xu, Fu-jiang Chen, Changchong Li, Weixi Zhang, Xiaofang Chen, Hui Chen
Abstract
Miao‐Shang Su, Manhuan Xu, Fu-jiang Chen, Changchong Li, Weixi Zhang, Xiaofang Chen, Hui Chen
Abstract
AIM: To isolate peripheric CD4(+) CD25(-) T cells in vitro, and study their biological characteristics. METHODS: Human peripheric blood CD4(+) CD25(-) T cells were isolated by discontinuous density gradient centrfugal and dynal immunomagnetic beads, and then divided into three groups: control group(A), LPS group (B) and LPS+TGF-beta1 mAb group (D), After they were prepared 4 h, 3 d and 5 d, the percentage of CD4(+) CD25(+) T cells were tested by FCM, the levels of TGF-beta1 in cultured supernatants were detected by ELISA, and the expression of FOXP3 mRNA was examined by RT-PCR. RESULTS: (1)LM showed CD4(+) CD25(-) T cells were of spherical cell nucleus, After CD4(+) CD25(-) T cells were cultured by anti-CD3/CD28 in vitro, their cellular volume increased and cytoplasm contained more particles. TEM showed CD4(+) CD25(-) T cells were of oval or kidney-shaped caryon. (2)FCM showed the purity of CD4(+) CD25(-) T cells was 91.5%-96%. The trypan blue experiment showed the energometry before and after detachment had no obvious difference(P>0.05). (3)FCM showed the percentage of CD4(+) CD25(+) T cells in B5d group(55.99+/-1.42)% increased markedly compared with that in A5d group(1.29+/-0.04)%. (4)ELISA showed the levels of TGF-beta1 in B3d(1.60+/-0.09) microg/L, in B5d(1.83+/-0.14) microg/L were significantly increased compared with those in A3d (0.35+/-0.04) microg/L and A5d(0.33+/-0.08) microg/L(P<0.01); but the levels in group D and group A had no significant difference; (5)RT-PCR showed FOXP3 mRNA in B3d group(0.84+/-0.07) and B5d group(1.85+/-0.24) increased strikingly compared with those in A3d(0.05+/-0.02) and A5d(0.04+/-0.02)(P<0.01), but those in group A and group D had no significant difference. (6)There was significantly positive correlation between the expression of TGF-beta1 and FOXP3 mRNA in the induced CD4(+) CD25(-) T cells (r=0.812, P<0.01). CONCLUSION: Human peripheric blood CD4(+) CD25(-) T cells can be isolated in vitro by discontinuous density gradient centrfugal and dynal immunomagnetic beads. The expression of FOXP3 mRNA in E.coli LPS-induced human CD4(+) CD25(-) T cells may correlate with the expression of TGF-beta1.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
AIM: To isolate peripheric CD4(+) CD25(-) T cells in vitro, and study their biological characteristics. METHODS: Human peripheric blood CD4(+) CD25(-) T cells were isolated by discontinuous density gradient centrfugal and dynal immunomagnetic beads, and then divided into three groups: control group(A), LPS group (B) and LPS+TGF-beta1 mAb group (D), After they were prepared 4 h, 3 d and 5 d, the percentage of CD4(+) CD25(+) T cells were tested by FCM, the levels of TGF-beta1 in cultured supernatants were detected by ELISA, and the expression of FOXP3 mRNA was examined by RT-PCR. RESULTS: (1)LM showed CD4(+) CD25(-) T cells were of spherical cell nucleus, After CD4(+) CD25(-) T cells were cultured by anti-CD3/CD28 in vitro, their cellular volume increased and cytoplasm contained more particles. TEM showed CD4(+) CD25(-) T cells were of oval or kidney-shaped caryon. (2)FCM showed the purity of CD4(+) CD25(-) T cells was 91.5%-96%. The trypan blue experiment showed the energometry before and after detachment had no obvious difference(P>0.05). (3)FCM showed the percentage of CD4(+) CD25(+) T cells in B5d group(55.99+/-1.42)% increased markedly compared with that in A5d group(1.29+/-0.04)%. (4)ELISA showed the levels of TGF-beta1 in B3d(1.60+/-0.09) microg/L, in B5d(1.83+/-0.14) microg/L were significantly increased compared with those in A3d (0.35+/-0.04) microg/L and A5d(0.33+/-0.08) microg/L(P<0.01); but the levels in group D and group A had no significant difference; (5)RT-PCR showed FOXP3 mRNA in B3d group(0.84+/-0.07) and B5d group(1.85+/-0.24) increased strikingly compared with those in A3d(0.05+/-0.02) and A5d(0.04+/-0.02)(P<0.01), but those in group A and group D had no significant difference. (6)There was significantly positive correlation between the expression of TGF-beta1 and FOXP3 mRNA in the induced CD4(+) CD25(-) T cells (r=0.812, P<0.01). CONCLUSION: Human peripheric blood CD4(+) CD25(-) T cells can be isolated in vitro by discontinuous density gradient centrfugal and dynal immunomagnetic beads. The expression of FOXP3 mRNA in E.coli LPS-induced human CD4(+) CD25(-) T cells may correlate with the expression of TGF-beta1.
Key concepts: IL-2 receptor, In vitro, Molecular biology, Trypan blue, FOXP3, Biology, CD3, Andrology