4 research outputs found
UVB radiation induced effects on cells studied by FTIR spectroscopy
We have made a preliminary analysis of the results about the eVects on
tumoral cell line (lymphoid T cell line Jurkat) induced by UVB radiation (dose
of 310 mJ/cm^2) with and without a vegetable mixture. In the present study, we
have used two techniques: Fourier transform infrared spectroscopy (FTIR) and
flow cytometry. FTIR spectroscopy has the potential to provide the
identiWcation of the vibrational modes of some of the major compounds (lipid,
proteins and nucleic acids) without being invasive in the biomaterials. The
second technique has allowed us to perform measurements of cytotoxicity and to
assess the percentage of apoptosis. We already studied the induction of
apoptotic process in the same cell line by UVB radiation; in particular, we
looked for correspondences and correlations between FTIR spetroscopy and flow
cytometry data finding three highly probable spectroscopic markers of apoptosis
(Pozzi et al. in Radiat Res 168:698-705, 2007). In the present work, the
results have shown significant changes in the absorbance and spectral pattern
in the wavenumber protein and nucleic acids regions after the treatments
Transcriptional Activation of Endogenous Retroviral Sequences in Human Epidermal Keratinocytes by UVB Irradiation.
Ultraviolet radiation is a pathogenic factor in various diseases, e.g., autoimmune disorders such as lupus erythematosus. On the other hand, endogenous retroviruses are discussed as etiologic agents in lupus erythematosus. Therefore, we investigated the influence of ultraviolet irradiation on expression of human endogenous retroviral sequences and human endogenous retroviral sequence promoter-driven transcription of cellular genes using human epidermal keratinocytes as a model system. First, conserved sequences of endogenous retroviral pol genes were amplified from cellular mRNA by reverse transcriptase polymerase chain reaction with degenerate oligonucleotide primers. Polymerase chain reaction products were hybridized in a reverse dot blot hybridization assay to a representative number of distinct cloned human endogenous retroviral pol fragments. Using this method, we could show that irradiation with 30 mJ per cm2 ultraviolet B activates transcription of various endogenous retroviral pol sequences in primary epidermal keratinocytes as well as in a spontaneously immortalized keratinocyte cell line (HaCaT). Interestingly, some of these sequences were found to be closely related to pol sequences of human endogenous retroviral sequences which have been shown to be expressed in autoimmune patients. Analysis of human endogenous retroviral pol expression in vivo using skin biopsies of lupus erythematosus patients revealed similar activation patterns. In a second approach, ultraviolet B- induced chimeric transcripts were isolated which are initiated by human endogenous retroviral promoters and proceed into cellular sequences using a newly established modified differential display polymerase chain reaction technique. The activation of human endogenous retroviral sequence transcription by ultraviolet B may contribute to the pathogenesis of lupus erythematosus, where inappropriate antigenic presentation of ultraviolet B-induced viral and cellular proteins could stimulate autoantibody production
Klinisch-biomedizinische Forschung an ausseruniversitaeren Einrichtungen der biomedizinischen Grundlagenforschung in Kooperation mit Hochschulkliniken KBF. Teilprojekt: Aktivierung endogener retroviraler Gene bei Autoimmunerkrankungen Schlussbericht
Available from TIB Hannover: F00B1332 / FIZ - Fachinformationszzentrum Karlsruhe / TIB - Technische InformationsbibliothekSIGLEBundesministerium fuer Bildung und Forschung, Berlin (Germany)DEGerman