2004•Journal of Clinical Laboratory ScienceRequires access

The effects of K562 on apoptosis of bone marrow stromal cells and secretion of TGF-β1 in vivro

Xiaoyun Pu

Open publisher page 0 citations

Abstract

Objective To investigate the effects of K562 on bone marrow stromal cells (BMSCs) by observing the alterations of apopotosis and the negative regulation of TGF-β1 secretion in separated culture and contact culture.Methods On the 2,4,7 and 12 day after culture the levels of TGF-β1 were measured by ELISA.The expression of TGF-β1 mRNA in BMSCs was determined by hybridization in situ.The apoptosis of BMSCs was detected by TUNEL.Results The quantity of normal BMSCs was significantly lower than that of control on day 12.The apoptosis of BMSCs in contact culture was significantly higher than that of control after 4 days (P0.01).The level of TGF-β1 was significantly higher than that of control after 4 days (P0.01).The positive rates of TGF-β1mRNA in normal BMSCs were significantly higher than that of control after 4 days (P0.01).Conclusion K562 inhibits apoptosis of BMSCs and upregulates the expression of TGF-β1,which may be one of the main factor that normal hemopoiesis is inhibited and hematopoietic microenvironments is injured by leukemia cells.

About this research paper

What this paper is about

Objective To investigate the effects of K562 on bone marrow stromal cells (BMSCs) by observing the alterations of apopotosis and the negative regulation of TGF-β1 secretion in separated culture and contact culture.Methods On the 2,4,7 and 12 day after culture the levels of TGF-β1 were measured by ELISA.The expression of TGF-β1 mRNA in BMSCs was determined by hybridization in situ.The apoptosis of BMSCs was detected by TUNEL.Results The quantity of normal BMSCs was significantly lower than that of control on day 12.The apoptosis of BMSCs in contact culture was significantly higher than that of control after 4 days (P0.01).The level of TGF-β1 was significantly higher than that of control after 4 days (P0.01).The positive rates of TGF-β1mRNA in normal BMSCs were significantly higher than that of control after 4 days (P0.01).Conclusion K562 inhibits apoptosis of BMSCs and upregulates the expression of TGF-β1,which may be one of the main factor that normal hemopoiesis is inhibited and hematopoietic microenvironments is injured by leukemia cells.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Objective To investigate the effects of K562 on bone marrow stromal cells (BMSCs) by observing the alterations of apopotosis and the negative regulation of TGF-β1 secretion in separated culture and contact culture.Methods On the 2,4,7 and 12 day after culture the levels of TGF-β1 were measured by ELISA.The expression of TGF-β1 mRNA in BMSCs was determined by hybridization in situ.The apoptosis of BMSCs was detected by TUNEL.Results The quantity of normal BMSCs was significantly lower than that of control on day 12.The apoptosis of BMSCs in contact culture was significantly higher than that of control after 4 days (P0.01).The level of TGF-β1 was significantly higher than that of control after 4 days (P0.01).The positive rates of TGF-β1mRNA in normal BMSCs were significantly higher than that of control after 4 days (P0.01).Conclusion K562 inhibits apoptosis of BMSCs and upregulates the expression of TGF-β1,which may be one of the main factor that normal hemopoiesis is inhibited and hematopoietic microenvironments is injured by leukemia cells.

Key concepts: Stromal cell, Haematopoiesis, Apoptosis, Bone marrow, TUNEL assay, Transforming growth factor, Secretion, K562 cells

Related papers

Back to paper searchBrowse research topicsOriginal source
The effects of K562 on apoptosis of bone marrow stromal cells and secretion of TGF-β1 in vivro — Research Paper | ScholarLens