International Journal of Clinical and Laboratory Research

, Volume 26, Issue 3, pp 143–159

Molecular, structural, and biological characteristics of the tumor necrosis factor ligand superfamily

Authors

  • H. -J. Gruss
    • Department of Internal Medicine IIIUniversity of Ulm Medical Center
Review

DOI: 10.1007/BF02592977

Cite this article as:
Gruss, H.-. Int J Clin Lab Res (1996) 26: 143. doi:10.1007/BF02592977
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Abstract

The tumor necrosis factor receptor superfamily at present consists of ten different transmembrane (type I) glycoproteins with characteristic limited sequence homology for the cysteine-rich repeats in the extracellular domain. In parallel the tumor necrosis factor ligand superfamily has been recognized by discovery of ligands for all members of the receptor superfamily. These molecules are also transmembrane (type II) glycoproteins, with the exception of lymphotoxin-α which is the only entirely secreted protein of the tumor necrosis factor-like proteins. Several members of the ligand superfamily, including tumor necrosis factor and CD95L also exist in a biologically active soluble form. The tumor necrosis factor ligand superfamily contains at present ten different proteins. In addition, NGFR p75 binds to a second family of proteins (neurotrophins). These nerve growth factor-like dimeric soluble molecules are basic neurotrophic factors and the five members (NGF, BDNF, NT-3, NT-4, NT-5) are not related to the tumor necrosis factor superfamily ligands. The members of the tumor necrosis factor ligand superfamily (TNF, LT-α, LT-β, CD27L, CD30L, CD40L, CD95L, 4-1BB, OX40L, TRAIL) share common biological activities, but some properties are shared by only some ligands, while others are unique. The diverse biological activities but some properties are shared by only some ligands, while others are unique. The diverse biological activities triggered through tumor necrosis factor receptors have been linked to the regulation of cellular activation, including immune responses and inflammatory reactions, but also with the pathology of a series of human diseases.

Key words

Tumor necrosis factorLigandsReceptorsBiologyHuman diseases

Copyright information

© Springer-Verlag 1996