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1.
The Journal of the Korean Academy of Periodontology ; : 375-388, 2000.
Artículo en Coreano | WPRIM | ID: wpr-77390

RESUMEN

The purpose of this study is to evaluate the expression ofIGF-I, considered as the mediator of action of estrogen, and IGF-IA and IGF-IB, alternative slicing form of IGF-I, using 17beta-estradiol in MC3T3-E1 cells. We observed the effect on type I collagen and osteopontin gene expression and DNA synthetic activity of MC3T3-E1 cells, added by estrogen, IGF-I and combination and the interaction on proliferation and differentiation of MC3T3-E1 cells. The results were as follows : RT-PCR experiment for observing time-dependant IGF-I gene expression patternshowed IGF-IA and IB gene expression in both of control and test group. In these IGF-IA gene expression was appeared predominantly. In control, IGF-I geneexpression level was maintained until 24hr and then decreased gradually. In test group, IGF-I gene expression level increased as time goes by. Experiment measuring DNA synthetic activity, as it is added by 17beta-estradiol, IGF-I and combination, showed that first day , there was the tendency of more increase of synthetic activity in all test group than control but no statical significance(P>0.05), and third day, there was more increase of DNA synthetic activity in 17beta-estradiol group and combination group and it was statically significant. (P<0.005) Experiment for observing type I collagen gene expression pattern showed more increase of expression in 17beta-estradiol group than control and no significant difference in IGF-I group and combination group. Experiment for observing osteopontin gene expression pattern showed no significant difference in control and test group. In conclusion, 17beta-estradiol in MC3T3-E1 cells increased IGF-I gene and DNA synthetic activity simultaneously, therefore it appeared that IGF-I is related to the action of estrogen. Combination treatment of IGF-I and 17beta-estradiol has effect on cell proliferation but this effect is lower than IGF-I or 17beta-estradiol alone. However, combination treatment has not great effect on type I collagen or osteopontin gene expression thus little effect of cell differentiation.


Asunto(s)
Matriz Ósea , Diferenciación Celular , Proliferación Celular , Colágeno Tipo I , ADN , Estrógenos , Expresión Génica , Factor I del Crecimiento Similar a la Insulina , Osteopontina
4.
Korean Journal of Pathology ; : 484-488, 1988.
Artículo en Coreano | WPRIM | ID: wpr-45459

RESUMEN

Multiple symmetric lipomatosis is a rare disease and affects almost exclusively middle aged man, usually with a background of excessive a alcohol intake. The disease is characterized by progressive growth of subcutaneous fat masses which are located symmetrically at neck, shoulders, chest, abdomen and groin, and which subsequently penetrate deeply into the surrounding spaces and structures with symptomatic compression of deep organs, such as trachea. A recent survey revealed a high incidence of sometic and autonomic neuropathy. The exact cause of the disease is not known, but a hyperplastic mechanism has been postulated, with in vitro studies demonstrating a defect in adrenergic-stimulated lipolysis of lipomatous tissue. We have experienced two cases of multiple symmetric lipomatosis. Case 1 was a 59-year-old male, complaining of slowly enlarging doughunt ring-shaped mass at his neck. He had a habit of excessive alcohol intake for many years. The subcutaneous mass at the neck was excised. The pathology report described the specimen as "normal adipose tissue". Case 2 was a 49-year-old male, complanining of slowly enlarging multiple symmetric masses at the neck, shoulders, chest, abdomen, flank and groin over a period of 6 years. He also complained of mild muscular weakness. He had a habit of excessive alcohol intake for many years. The subcutaneous mass in the neck was excised. The specimen had a tendency to form globular masses and microscopically indistinguishable from mature adipose tissue.


Asunto(s)
Incidencia
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