LST1: A gene with extensive alternative splicing and immunomodulatory function

Ingrid Rollinger-Holzinger*, Brigitte Eibl, Marc Pauly, Ute Griesser, François Hentges, Bernhard Auer, Georg Pall, Peter Schratzberger, Dietger Niederwieser, Elisabeth H. Weiss, Heinz Zwierzina

*Corresponding author for this work

Research output: Contribution to journalArticleResearchpeer-review

50 Citations (Scopus)


The gene of the leukocyte-specific transcript (LST1) is encoded within the TNF region of the human MHC. The LST1 gene is constitutively expressed in leukocytes and dendritic cells, and it is characterized by extensive alternative splicing. We identified 7 different LST1 splice variants in PBMC; thus, 14 LST1 splice variants (LST1/A-LST1/N) have been detected in various cell types. These isoforms code for transmembrane as well as soluble LST1 proteins characterized by two alternative open reading frames at their 3' end. We demonstrate the presence of the transmembrane variant LST1/C on the cell surface of the monocytic cell lines U937 and THP1. Recombinant expression of LST1/C permitted its profound inhibitory effect on lymphocyte proliferation to be observed. In contrast, the alternative transmembrane variant LST1/A, the extracellular domain of which shows no amino acid sequence homology to LST1/C exerted a weaker but similar inhibitory effect on PBMC. These data demonstrate the protein expression of LST1 on the cell surface of mononuclear cells, and they show an inhibitory effect on lymphocyte proliferation of two LST1 proteins although they have only a very short amino acid homology.

Original languageEnglish
Pages (from-to)3169-3176
Number of pages8
JournalJournal of Immunology
Issue number6
Publication statusPublished - 15 Mar 2000
Externally publishedYes


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