
%0 Journal Article
%A Hornen, N. 
%A Kues, W. A. 
%A Niemann, H. 
%T 282 CHARACTERIZATION OF THE DEVELOPMENTAL POTENTIAL OF FETAL SOMATIC STEM CELLS ISOLATED FROM DIFFERENT TISSUES
%J Reproduction, Fertility and Development
%D 2007/12/12
%V 20
%N 1
%P 221-221
%K 
%R https://doi.org/10.1071/RDV20N1AB282
%U https://www.publish.csiro.au/paper/RDV20N1AB282 
%X Recently we discovered a novel type of stem cells which can be derived from primary cultures of fetal connective tissue using a high-density culture (HD) system (Kues et al. 2005 Biol. Reprod. 70, 1020&#8211;1028). This cell type shows most of the characteristics of true embryonic stem cells and is a promising alternative for developing therapeutically useful cells. The goal of the present study was to analyze and characterize stem cell populations obtained from five different tissues, i.e., brain, heart, lung, liver, and adrenal gland, using this HD culture system. Explant cultures of the double transgenic strain OG2/Rosa26 were established from mouse fetuses at Day 13.5 post-conception. In this strain, cells with pluripotent properties are characterized by the green fluorescence of the green fluorescent protein (GFP) which is under the transcriptional control of the Oct-4 promoter. In a total of five replicates, cells were subcultivated and reseeded at a concentration of 25 000 cells/cm&#8211;2. Cell culture conditions were as recently reported for fetal somatic stem cell derivation (Kues et al. 2005 Biol. Reprod. 72, 1020&#8211;1028). After colony formation and/or observation of green fluorescence under UV illumination, mRNA was isolated for RT-PCR analysis of the expression of genes known to be involved in pluripotency, i.e., Oct-4, Nanog, Stat3, TNAP, Rex1, and Sox2. Under these culture conditions, 12.5% of the liver and 80% of the brain explants showed senescence and could not be seeded at the required concentration. No colony formation was observed in brain and heart cultures. Cells from heart explants showed a three-dimensional growth over the whole surface of the attached cells and were difficult to separate. On average, colony formation was observed after 11 days ± 8 (mean ± SD) (fetal fibroblasts), 10 days ± 7 (lung), 18 days ± 11 (liver), and 4 days ± 1 (adrenal gland). Green fluorescence was detected after 17 days ± 9 (fetal fibroblasts), 17 days ± 9 (lung), 35 days ± 13 (heart, randomly distributed), 26 days ± 10 (brain), 26 days ± 8 (liver), and 8 days ± 5 (adrenal gland). A single large clump of stem-like cells formed in 43% of the fetal fibroblast, 35% of the lung, and 41% of the liver derivatives. Oct-4 expression was not observed in any of the cultures. Nanog and Stat3 were expressed in all cell cultures, and TNAP was expressed in all cultures from heart, brain, lung, and adrenal gland. Rex1 was expressed in all cultures from brain and adrenal gland, and in 25% of the heart cultures and in 16.6% of the fetal fibroblasts. Sox2 was expressed in all cultures from brain and in 16.6% of fetal fibroblast cultures. These preliminary results show that cells with some of the typical features of stem cells can be derived from various tissues of the body, but that the efficiency is different among tissues. Only cells derived from the adrenal gland exhibited better colony formation than the original fibroblasts.  This work was funded by DFG grant Ni 256/28-1. 
