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Stromal cells from murine developing hemopoietic organs: comparison of colony forming unit of fibroblasts and long term cultures

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Figure

Fig. 2. Adherentmarrowafter different
Fig. 3. Characterizationof stromalpositive cells is expressedcellsgrownfromfetalliver,neonatalliver, neonataland adult bone marrow.Thenumber of coloniescontaining alkaline phosphatase,acid phosphatase,and myeloperoxidase- as a percentage of the totalnumber of coloniesexamined.Rela,tiveamounts(arrhe presenceof alkaline phosphataseandmye/operoxidasepositive cells in the adherent layers of long-term culturesare shown.
Fig. 4. Presenceof glycosaminoglycansfibroblastfrom differentpositive for GAGsAfter comparison(sulfatedand non-sulfated)incoloniesandstromalcells of long-termculturesderivedhemopoieticorgans.The number of colonies which stain is expressedas a percentageof
Fig. 5. The presenceof intra-andextracellularfibronectinin l TC is shownusing (AI rhe PAP-technique.the presenceof fibronectinis expressedinrelative amounts; (B) the ELISA technique:the amountof fibronectinisexpressedin ng per well.

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