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Thyroid Hormone Induces Apoptosis in Primary Cell Cultures of Tadpole Intestine: Cell Type Specificity and Effects of Extracellular Matrix

Thyroid hormone (T(3) or 3,5,3′-triiodothyronine) plays a causative role during amphibian metamorphosis. To investigate how T(3) induces some cells to die and others to proliferate and differentiate during this process, we have chosen the model system of intestinal remodeling, which involves apoptot...

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Detalles Bibliográficos
Autores principales: Su, Yuan, Shi, Yufang, Stolow, Melissa A., Shi, Yun-Bo
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1997
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2132612/
https://www.ncbi.nlm.nih.gov/pubmed/9396758
Descripción
Sumario:Thyroid hormone (T(3) or 3,5,3′-triiodothyronine) plays a causative role during amphibian metamorphosis. To investigate how T(3) induces some cells to die and others to proliferate and differentiate during this process, we have chosen the model system of intestinal remodeling, which involves apoptotic degeneration of larval epithelial cells and proliferation and differentiation of other cells, such as the fibroblasts and adult epithelial cells, to form the adult intestine. We have established in vitro culture conditions for intestinal epithelial cells and fibroblasts. With this system, we show that T(3) can enhance the proliferation of both cell types. However, T(3) also concurrently induces larval epithelial apoptosis, which can be inhibited by the extracellular matrix (ECM). Our studies with known inhibitors of mammalian cell death reveal both similarities and differences between amphibian and mammalian cell death. These, together with gene expression analysis, reveal that T(3) appears to simultaneously induce different pathways that lead to specific gene regulation, proliferation, and apoptotic degeneration of the epithelial cells. Thus, our data provide an important molecular and cellular basis for the differential responses of different cell types to the endogenous T(3) during metamorphosis and support a role of ECM during frog metamorphosis.