Fig. 3.
Fig. 3. (A through C) Cytospin analysis of flASK cells. (A) Cytospin preparations of flASK cells immediately after cell sorting or after suspension culture in (B) control CM plus 25 ng/mL KL or (C) WNT-5a CM plus KL. (D and E) Formation of adherent hematopoietic foci after cells were plated onto fibronectin-coated glass chamber slides and cultured for 4 days. Cells were fixed and stained in situ to preserve the intercellular organization of the foci. (D) Control CM plus 25 ng/mL KL. (E) WNT-5a CM (gDWnt5a) plus 25 ng/mL KL. Notice that, in (E), WNT-5a CM results in a dramatic enhancement of foci formation in which blast cells are found as adherent clusters overlying adherent cells.

(A through C) Cytospin analysis of flASK cells. (A) Cytospin preparations of flASK cells immediately after cell sorting or after suspension culture in (B) control CM plus 25 ng/mL KL or (C) WNT-5a CM plus KL. (D and E) Formation of adherent hematopoietic foci after cells were plated onto fibronectin-coated glass chamber slides and cultured for 4 days. Cells were fixed and stained in situ to preserve the intercellular organization of the foci. (D) Control CM plus 25 ng/mL KL. (E) WNT-5a CM (gDWnt5a) plus 25 ng/mL KL. Notice that, in (E), WNT-5a CM results in a dramatic enhancement of foci formation in which blast cells are found as adherent clusters overlying adherent cells.

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