Accession Number	<strong>00042737-200107000-00005</strong>.
Author	Schuchmann, Marcus; Galle, Peter R.
Institution	Department of Internal Medicine I, Johannes Gutenberg University, Mainz, Germany
Title	Apoptosis in liver disease.[Review]
Source	European Journal of Gastroenterology & Hepatology. 13(7):785-790, July 2001.
Abstract	A variety of biological functions are regulated through extracellular signals. Amongst the best studied examples is growth control, which is achieved by the regulatory function of growth factors. In recent years it has become apparent that cell death (apoptosis) is controlled in a similar fashion. Apoptosis, firstly a morphologically defined process, is a highly controlled type of cell death that plays a critical role in embryonic development, deletion of autoreactive T-cells and adult tissue homoeostasis. There is increasing evidence that derangement of the apoptotic program is the underlying cause of a series of diseases including liver diseases. The deadly program can be initiated by ligand binding to membrane bound receptors such as CD95 (Fas), which is the most prominent cell death inducing member of the TNF receptor superfamily. The core of the subsequently activated intracellular machinery is formed by a set of proteases, namely caspases. Once activated, they orchestrate the complete destruction of the cellular skeleton leading to the typical apoptotic morphology. This review foucuses on the underlying mechanism leading to derangement of the usually highly controlled apoptotic program in different liver diseases. (C) 2001 Lippincott Williams & Wilkins, Inc.