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Biomedical subjects

C Lamping

Publications and source records attributed to C Lamping.

5 recordsLinked to original sources

Biologic indicators of exposure: are markers associated with oncogenesis useful as biologic markers of effect?

Radiation-induced molecular and cellular alterations play an important role in the transformation of a normal cell into a cancer cell. However, the basic molecular and cellular alterations upon exposure to ionizing irradiation are still poorly understood. Identification of such alterations would be of importance for the assessment of exposure dose, as well as for the assessment of an exposed individual's risk of developing cancer. Extensive studies of the mechanisms of oncogenesis have led to the identification of altered genes, such as proto-oncogenes and tumor suppressor genes as well as other genes intimately involved in cellular proliferation and differentiation, that are more or less frequently associated with a variety of human malignancies. It can be assumed that at least some of these mechanisms are associated with radiation-induced oncogenesis. The longevity of stem cells, particularly those of the hemopoietic system, makes them the prime target cell population to accumulate genetic alterations due to exposure to a variety of agents. Improvements in purification strategies for hemopoietic stem cells, as well as the availability of sensitive techniques such as the polymerase chain reaction (PCR) and flow cytometry analysis, should allow in-depth studies at the molecular and cellular level after exposure to physical and chemical agents.

Animals↗

The effect of recombinant human stem cell factor and basic fibroblast growth factor on the in vitro radiosensitivity of CD34+ hematopoietic progenitors from human umbilical cord blood.

Human umbilical cord blood (CB) cells selected by immunomagnetic beads for expression of the CD34 antigen were irradiated with increasing doses of x-rays (72 cGy/min). Clonogenic survival of the hematopoietic progenitors, including mixed colony-forming cells (Mix-CFC), erythroid burst-forming units (BFU-E), and granulocyte-macrophage colony-forming cells (GM-CFC), was determined in methylcellulose cultures containing placenta conditioned medium (PCM) and erythropoietin (Epo). Exponential survival curves were fitted to the data of all the colonies, resulting in D0 = 95 cGy for Mix-CFC, 136 cGy for BFU-E, and 136 cGy for GM-CFC. Additionally, the radiosensitivity of CD34+ cells was studied employing cultures containing either recombinant human stem cell factor (rhSCF) or basic fibroblast growth factor (b-FGF) in combination with PCM and Epo. It was found that the colony-forming efficiency (CFE) of non-irradiated CD34+ cells of 5.5% (range 1.4 to 14.4%) did not increase after the addition of SCF or b-FGF to the culture. The radiation response characteristics showed, however, that in the presence of SCF, the D0 value and the extrapolation number n increased significantly. This suggests the stimulation of what operationally is termed "recovery from potentially lethal damage." In contrast, no response modifying effect could be seen for b-FGF.

Antigens, CD↗

Single-cell cDNA-PCR: removal of contaminating genomic DNA from total RNA using immobilized DNase I.

A procedure utilizing immobilized DNase I that allows the efficient amplification of cDNA by PCR from a single cell in the absence of contaminating genomic DNA is described. DNase I treated, total RNA derived from single cells was reverse transcribed into cDNA followed by PCR using beta-actin and c-fos specific primers that recognize different exons of the respective genes. Amplification products corresponding to cDNA, but not to genomic sequences, were detected after treatment with immobilized DNase I in samples previously shown to be contaminated with genomic DNA. This method allows the efficient removal of DNA contaminating total RNA derived from a single cell.

Artifacts↗