Method for in vitro expansion of erythroid cells

Abstract

The present invention relates to a method for in vitro expansion of mature erythroid cells. More specifically, the present invention relates to a method for obtaining concentrated erythrocytes by culturing erythroid cells at high density so as to allow the cells to physically and directly come in contact with each other. Particularly, the method of the present invention is very useful in that it is possible to obtain a large amount of clinically useful concentrated erythrocytes through a small container such as a test tube-sized bioreactor.

1 . A method for in vitro expansion of erythroid cells, including culturing erythroid cells at a high density such that the cells come into direct physical contact with each other or in the presence of ICAM-4 protein. 
     
     
         2 . The method according to  claim 1 , wherein the erythroid cells are those that exit the terminal maturation stage. 
     
     
         3 . The method according to  claim 1 , wherein the high-density culture is performed at 100-200% confluence. 
     
     
         4 . The method according to  claim 1 , wherein the erythroid cells in direct physical contact with each other express at least one gene selected from adhesion-related genes DLC-1, ICAM-4, and VLA-4. 
     
     
         5 . The method according to  claim 4 , wherein the signal exchange between the cells is activated by the expression of the gene to increase the productivity of red blood cells. 
     
     
         6 . The method according to  claim 4 , wherein the binding and signal transduction between the erythroid cells are stimulated via ICAM-4 protein to be expressed. 
     
     
         7 . The method according to  claim 1 , wherein the culture in the presence of ICAM-4 protein is performed by the introduction of an ICAM-4 expression vector or the addition of ICAM-4 protein. 
     
     
         8 . The method according to  claim 1 , further comprising adding DLC-1 or VLA-4 protein to a culture medium of the erythroid cells. 
     
     
         9 . The method according to  claim 1 , Wherein the erythroid cells are cultured in a 2D or 3D configuration. 
     
     
         10 . The method according to  claim 9 , wherein the erythroid cells are cultured in a 3D configuration in a state in which the erythroid cells are allowed to settle and packed. 
     
     
         11 . A marker composition for erythroid cell differentiation comprising DLC-1. 
     
     
         12 . The marker composition according to  claim 11 , wherein the DLC-1 consists of the amino acid sequence set forth in SEQ ID NO. 1. 
     
     
         13 . The marker composition according to  claim 11 , wherein the DLC-1 binds to VLA-4 to emit adhesion-related signals. 
     
     
         14 . The marker composition according to  claim 11 , further comprising ICAM-4. 
     
     
         15 . A method for increasing the maturation of erythroid cells, comprising promoting the expression or activity of DLC-1, VLA-4, and ICAM-4. 
     
     
         16 . The method according to  claim 14 , wherein the maturation of the erythroid cells comprises enucleation. 
     
     
         17 . The method according to  claim 15 , wherein the expression or activity of DLC-1, VLA-4 and ICAM-4 is promoted by the introduction of DLC-1, VLA-4, and ICAM-4 genes into the erythroid cells. 
     
     
         18 . A method for in vitro expansion of erythroid cells, comprising the method for increasing the maturation of erythroid cells according to  claim 15 .