[Frontiers in Bioscience 14, 657-664, January 1, 2009]

Recent progress in research on beta-cell apoptosis by cytokines

Kyoung-Ah Kim1, Myung-Shik Lee2

1Department of Medicine, Dongguk University International Hospital, Dongguk University School of Medicine, Goyang, Korea 2Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea

TABLE OF CONTENTS

1. Abstract
2. Introduction
3. Role of NF-k B in b cell death in T1DM
4. Role of NF-k B-mediated XIAP upregulation againstb cell apoptosis
5. Role of STAT1 in b cell apoptosis
6. Perspective
7. Acknowledgements
8. References

1. ABSTRACT

Pancreatic beta-cell apoptosis plays a critical role in the pathogenesis of type 1 diabetes mellitus. As death effector molecules, perforin, Fas ligand, tumor necrosis factor (TNF)-alpha, Interleukin (IL)-1, interferon (IFN)-gamma, and nitric oxide have been claimed. Recently, combinations or synergisms between IFN-gamma and TNF-alpha or IL-1b are being revisited as the death effectors, and signal transduction of such synergisms has been explored to find molecular mechanism of beta -cell death. Among the regulators of apoptosis, nuclear factor-kappaB (NF-kappaB) has emerged as a master switch of cytokine-induced beta -cell dysfunction and death. By employing TNF-alpha / IFN-gamma synergism model which causes beta -cell apoptosis, we found that the antiapoptotic X-linked inhibitor of apoptosis (XIAP) molecule is upregulated by NF-kappaB in response to TNF-alpha and XIAP induction was inhibited by IFN-gamma-induced signal transducer and activator of transcription-1 (STAT1) activation, which explains the death of beta -cells by TNF-alpha /IFN-gamma synergism.