Clonal heterogeneity in fibroblast cultures from donors of all ages has been associated with differentiation of the fibroblast/fibrocyte system. Thus, a terminal differentiation lineage including a sequence of three potentially mitotic progenitor fibroblasts (MFI --> MFII --> MFIII) in the precursor compartment and three types of postmitotic fibrocytes (PMFIV --> PMFV --> PMFVI) in the functional compartment has been identified previously. In the present study, we show that replenishment of fibrocytes lost from the functional compartment is not expected to change the distribution of differentiation types in a steady state population, provided cell loss occurs at the end of a long sequence of cell divisions only. However, premature terminal differentiation of progenitor fibroblasts to postmitotic fibrocytes can be induced by ionising radiation and other cell stressors, Furthermore, even a low dose of 1 Gy causes a change in the distribution of surviving MF progenitor cells towards later differentiation stages within the precursor compartment. The role of autocrine transforming growth factor-beta1 production by fibroblasts in mediating terminal differentiation was investigated. We propose that cell stress and DNA damaging agents may contribute to progression of the differentiation state with age and that individual variation may be related to differences in the rate of induced differentiation. (C) 2000 Elsevier Science Inc. All rights reserved.
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Heidelberg Univ, Med Fak Mannheim, Univ Med Mannheim, Klin Strahlentherapie & Radioonkol, Mannheim, GermanyHeidelberg Univ, Med Fak Mannheim, Univ Med Mannheim, Klin Strahlentherapie & Radioonkol, Mannheim, Germany
Herskind, C.
Sticht, C.
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Heidelberg Univ, Med Fak Mannheim, Univ Med Mannheim, Zentrum Med Forsch, Mannheim, GermanyHeidelberg Univ, Med Fak Mannheim, Univ Med Mannheim, Klin Strahlentherapie & Radioonkol, Mannheim, Germany
Sticht, C.
Sami, A.
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Heidelberg Univ, Med Fak Mannheim, Univ Med Mannheim, Klin Strahlentherapie & Radioonkol, Mannheim, GermanyHeidelberg Univ, Med Fak Mannheim, Univ Med Mannheim, Klin Strahlentherapie & Radioonkol, Mannheim, Germany
Sami, A.
Giordano, F. A.
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Heidelberg Univ, Med Fak Mannheim, Univ Med Mannheim, Klin Strahlentherapie & Radioonkol, Mannheim, GermanyHeidelberg Univ, Med Fak Mannheim, Univ Med Mannheim, Klin Strahlentherapie & Radioonkol, Mannheim, Germany
Giordano, F. A.
Wenz, F.
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Heidelberg Univ, Med Fak Mannheim, Univ Med Mannheim, Klin Strahlentherapie & Radioonkol, Mannheim, Germany
Univ Klinikum Freiburg, Freiburg, GermanyHeidelberg Univ, Med Fak Mannheim, Univ Med Mannheim, Klin Strahlentherapie & Radioonkol, Mannheim, Germany