inosine-diphosphate and Scleroderma--Systemic

In the present study, we attempted to identify the chemical nature of the clastogenic factor (CF) from patients with progressive systemic sclerosis (scleroderma). Computerized mass spectrometry of clastogenic fractions obtained by HPLC of plasma ultrafiltrates detected molecular peaks compatible with inosine triphosphate and inosine diphosphate (ITP and IDP). The concomitant detection of IDP, together with ITP, and the absence of these peaks in nonclastogenic fractions and corresponding control fractions are arguments in favor of a biological relevance of these observations. The most important confirmation came from the clastogenic effect of commercial ITP and IDP added to the culture medium of the test cultures. The induction of chromatid type damage by these substances in lymphocytes exposed in the G0 phase of their cell cycle and the prevention of this damage by superoxide dismutase are analogous to the observations with CF.

Topics: Cells, Cultured; Chromatography, High Pressure Liquid; Chromosome Aberrations; Humans; Inosine Diphosphate; Inosine Nucleotides; Inosine Triphosphate; Lymphocytes; Mass Spectrometry; Mutagens; Reference Values; Ribonucleotides; Scleroderma, Systemic; Sister Chromatid Exchange; Superoxide Dismutase