Effect of low dose MIP-1α combined IL-8 on clone formation of hurman lone marrow hematopoietic cells
Li Zhao
Abstract
Li Zhao
Abstract
Objective To study the effect of low dose Macrophage inflamatory prolein α (MIP 1α) combined with IL 8 on clone formation of human bone marrow hematopoietic cells. Methods Bone marrow hematopoietic cells were divided into 5 groups: control group (with no MIP α or IL 8) , 10 mg/ml combination group (with 10 ng/ml MIP lx and 10 ng/ml IL 8), 1 mg/ml combination group (with 1 ng/ml MIP lα and 1 ng/ml IL 8) ,MIP lα group (with 20 ng/ml MIP), and IL 8 group (with 20 ng/ml IL 8). Then these cells were cultivated in 0 9% methyl cellulose system. Several days later, count the clones of CFU GM, CFU E and CFU Mix of each group. Results At the concentration of 1 ng/ml, combination of MIP 1α and IL 8 didn't inhibit the clone formation but the 10 ng/ml combination group did obviously. Neither MIP 1α nor IL 8 alone did it in our study. Conclusion Combination of MIP 1α and IL 8 both at 10 ng/ml can coordinate each other to inhibit the clone formation of human bone marrow hematopoietic cells.
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.
Objective To study the effect of low dose Macrophage inflamatory prolein α (MIP 1α) combined with IL 8 on clone formation of human bone marrow hematopoietic cells. Methods Bone marrow hematopoietic cells were divided into 5 groups: control group (with no MIP α or IL 8) , 10 mg/ml combination group (with 10 ng/ml MIP lx and 10 ng/ml IL 8), 1 mg/ml combination group (with 1 ng/ml MIP lα and 1 ng/ml IL 8) ,MIP lα group (with 20 ng/ml MIP), and IL 8 group (with 20 ng/ml IL 8). Then these cells were cultivated in 0 9% methyl cellulose system. Several days later, count the clones of CFU GM, CFU E and CFU Mix of each group. Results At the concentration of 1 ng/ml, combination of MIP 1α and IL 8 didn't inhibit the clone formation but the 10 ng/ml combination group did obviously. Neither MIP 1α nor IL 8 alone did it in our study. Conclusion Combination of MIP 1α and IL 8 both at 10 ng/ml can coordinate each other to inhibit the clone formation of human bone marrow hematopoietic cells.
Key concepts: clone (Java method), Bone marrow, Haematopoiesis, CFU-GM, Molecular biology, Chemistry, Immunology, Biology