scholarly journals Clonal origin of human erythro-eosinophilic colonies in culture

Blood ◽  
1982 ◽  
Vol 59 (4) ◽  
pp. 857-864 ◽  
Author(s):  
T Nakahata ◽  
SS Spicer ◽  
M Ogawa

Abstract We have observed the presence of erythropoietic bursts containing eosinophils and their precursors in methylcellulose culture of human peripheral blood and marrow nucleated cells in the presence of erythropoietin and medium conditioned by phytohemagglutinin-stimulated leukocytes (PHA-LCM). It was possible to identify these bursts (colonies) in situ in methylcellulose culture on the basis of their unique red and black colors. Transmission electron microscopy revealed that the constituent erythroid and eosinophilic cells lay intermixed with each other, and through close intercellular connections formed compact colonies and bursts consisting of several sub-colonies. Differential counts of individual erythro-eosinophil colonies (EEo colonies) revealed only a small percentage of blast cells in most of the colonies. Replating experiments of single EEo colonies yielded only eosinophilic colonies and clusters and erythroid colonies. The clonal nature of the EEo colonies was documented by analysis of Y-chromatin- positive cells in individual EEo colonies derived from cocultures of male and female peripheral blood mononuclear cells. Comparison of conditioned media indicated that PHA-LCM is the best stimulator for EEo colonies. These studies suggest that the differentiation capabilities of the progenitors for EEo colonies are restricted to erythroid and eosinophilic differentiation.

Blood ◽  
1982 ◽  
Vol 59 (4) ◽  
pp. 857-864 ◽  
Author(s):  
T Nakahata ◽  
SS Spicer ◽  
M Ogawa

We have observed the presence of erythropoietic bursts containing eosinophils and their precursors in methylcellulose culture of human peripheral blood and marrow nucleated cells in the presence of erythropoietin and medium conditioned by phytohemagglutinin-stimulated leukocytes (PHA-LCM). It was possible to identify these bursts (colonies) in situ in methylcellulose culture on the basis of their unique red and black colors. Transmission electron microscopy revealed that the constituent erythroid and eosinophilic cells lay intermixed with each other, and through close intercellular connections formed compact colonies and bursts consisting of several sub-colonies. Differential counts of individual erythro-eosinophil colonies (EEo colonies) revealed only a small percentage of blast cells in most of the colonies. Replating experiments of single EEo colonies yielded only eosinophilic colonies and clusters and erythroid colonies. The clonal nature of the EEo colonies was documented by analysis of Y-chromatin- positive cells in individual EEo colonies derived from cocultures of male and female peripheral blood mononuclear cells. Comparison of conditioned media indicated that PHA-LCM is the best stimulator for EEo colonies. These studies suggest that the differentiation capabilities of the progenitors for EEo colonies are restricted to erythroid and eosinophilic differentiation.


Author(s):  
M. A. Greenwood ◽  
G. R. Hook ◽  
D. Barba ◽  
B. Ikejiri ◽  
S. N. Chen ◽  
...  

In the previous abstract, we presented data on the cytolysis of glioma-derived cells (SNB-92) by lymphokine activated mononuclear cells (LAK). In this abstract, we describe our transmission electron microscopy (TEM) study of the interaction of LAK cells and SNB-92 in vitro during a time sequence of 5 minutes to 4 hours. Co-cultures were fixed in situ by the direct addition to the culture medium of 2.5% glutaraldehyde and prepared in a routine manner for TEM.Within 30 minutes, some cells within the LAK population make contact with glioma cells (Fig 1). These LAK cells assume an elongated shape when they approach their target. The nucleus is asymmetrically located distal to the point of contact. The cellular organelles and microtubules orient towards the target cell. The plasma membranes of both cells bind closely together and form numerous interdigitations.


Sign in / Sign up

Export Citation Format

Share Document