RESUMEN
The Good Neighbor Project is aimed at eliminating cultural and social barriers by recruiting and educating volunteers from African-American churches to provide in-home services for indigent, geriatric, African-American patients with cancer in Oakland, Calif. Volunteers' knowledge about and attitude toward cancer before and after their participation in the project were determined by a survey.
Asunto(s)
Negro o Afroamericano , Cuidadores , Conocimientos, Actitudes y Práctica en Salud , Neoplasias/enfermería , Apoyo Social , Voluntarios , Adolescente , Adulto , Negro o Afroamericano/educación , Negro o Afroamericano/psicología , California , Atención Domiciliaria de Salud , Humanos , Indigencia Médica , Persona de Mediana Edad , Religión , Encuestas y Cuestionarios , Voluntarios/educación , Voluntarios/psicologíaRESUMEN
We constructed a double-stranded plasmid containing a single cis, syn-cyclobutane thymine dimer (T[c,s]T) 385 base pairs from the center of the SV40 origin of replication. This circular DNA was replicated in vitro by extracts from several types of human cells. The dimer was placed on the leading strand template of the first replication fork to encounter the lesion. Two-dimensional gel electrophoresis of replication intermediates documented the transient arrest of the replication fork by the dimer. Movement of the replication fork beyond the dimer was recognized by the appearance of a single fork arc in DNA sequences located between the T[c,s]T and the half-way point around the circular template (180 degrees from the origin). Upon completion of plasmid replication, the T[c,s]T was detected by T4 endonuclease V in about one-half (46 +/- 9%) of the closed circular daughter molecules. Our results demonstrate that extracts prepared from HeLa cells and SV40-transformed human fibroblasts (SV80, IDH4), including a cell line defective in nucleotide-excision repair (XPA), were competent for leading strand DNA synthesis opposite the pyrimidine dimer and replication fork bypass. In contrast, dimer bypass was severely impaired in otherwise replication-competent extracts from two different xeroderma pigmentosum variant cell lines.
Asunto(s)
Replicación del ADN , Dímeros de Pirimidina/metabolismo , Catálisis , Daño del ADN , Enzimas de Restricción del ADN/metabolismo , Electroforesis en Gel Bidimensional , Células HeLa , Humanos , Técnicas In Vitro , Modelos Genéticos , Plásmidos/metabolismo , Virus 40 de los Simios , Xerodermia Pigmentosa/genéticaAsunto(s)
Adhesión Celular/genética , Adhesión Celular/fisiología , Integrinas/fisiología , Animales , Regulación de la Expresión Génica , Genes Inmediatos-Precoces , Humanos , Técnicas In Vitro , Integrinas/genética , Monocitos/citología , Monocitos/fisiología , Biosíntesis de Proteínas , ARN Mensajero/genética , ARN Mensajero/metabolismo , Factores de Transcripción/metabolismo , Transcripción Genética , Activación TranscripcionalRESUMEN
Colony stimulating factor-1 (CSF-1) is a homodimeric glycoprotein that humorally regulates the proliferation and differentiation of mononuclear phagocytic cells and locally regulates cells of the female reproductive tract. Alternative splicing of the human CSF-1 mRNA leads to alternative expression of the CSF-1 homodimer as a secreted glycoprotein or as a membrane-spanning molecule with cell surface biological activity. In the present study, analysis of immunoaffinity-purified CSF-1 from mouse L929 cell medium by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) indicated that CSF-1 is predominantly secreted as highly sulfated species of 375- and 250-kDa with a smaller amount of a 100-kDa species. Analysis by gel filtration in 4 M guanidine HCI buffer, indicated that, in contrast to the 100-kDa species, the highly sulfated species exhibit anomalously high molecular weights and self-association on SDS-PAGE similar to the dermatan sulfate proteoglycan, biglycan. The three predominant CSF-1 species were shown to be an 80-kDa homodimer, an 80-kDa/50-kDa heterodimer, and a 50-kDa homodimer. The 80-kDa subunit contained a single 18-kDa chondroitin sulfate chain that was absent from the 50-kDa subunit. Furthermore, treatment of the 80- and 50-kDa subunits, synthesized in the presence of tunicamycin, with chondroitinase ABC, neuraminidase, and endo-alpha-N-acetyl galactosaminidase reduced their apparent molecular masses to 60 and 25 kDa, respectively. These results are consistent with intracellular proteolytic cleavage of the 80-kDa chondroitin sulfate containing subunits from the membrane spanning CSF-1 precursor at a point carboxyl-terminal to the single consensus sequence for glycosaminoglycan addition and cleavage of the 50-kDa glycoprotein subunit at a position aminoterminal to this site. The predominance of the proteoglycan form of secreted CSF-1, which represents only 3-4% of the total trichloroacetic acid-precipitable counts released from 35SO4(2-)-labeled L cells, has important implications for regulation by this growth factor.