Rf. Pereira et al., CULTURED ADHERENT CELLS FROM MARROW CAN SERVE AS LONG-LASTING PRECURSOR CELLS FOR BONE, CARTILAGE, AND LUNG IN IRRADIATED MICE, Proceedings of the National Academy of Sciences of the United Statesof America, 92(11), 1995, pp. 4857-4861
Cells from transgenic mice expressing a human mini-gene for collagen I
were used as markers to follow the fate of mesenchymal precursor cell
s from marrow that were partially enriched by adherence to plastic, ex
panded in culture, and then injected into irradiated mice, Sensitive P
CR assays for the marker collagen I gene indicated that few of the don
or cells were present in the recipient mice after 1 week, but 1-5 mont
hs later, the donor cells accounted for 1.5-12% of the cells in bone,
cartilage, and lung in addition to marrow and spleen, A PCR in situ as
say on lung indicated that the donor cells diffusely populated the par
enchyma, and reverse transcription-PCR assays indicated that the marke
r collagen I gene was expressed in a tissue-specific manner, The resul
ts, therefore, demonstrated that mesenchymal precursor cells from marr
ow that are expanded in culture can serve as long-lasting precursors f
or mesenchymal cells in bone, cartilage, and lung, They suggest that c
ells may be particularly attractive targets for gene therapy ex vivo.