Human CD38 and its ligand CD31 define a unique lamina propria T lymphocyte signaling pathway
2001; Wiley; Volume: 15; Issue: 3 Linguagem: Inglês
10.1096/fj.00-0522fje
ISSN1530-6860
AutoresSilvia Deaglio, Roberto Mallone, Germano Baj, Danilo Donati, Giorgio Giraudo, F Corno, Santina Bruzzone, Massimo Geuna, Clara Maria Ausiello, Fabio Malavasi,
Tópico(s)Cytomegalovirus and herpesvirus research
ResumoCD38, a nonlineage-restricted surface glycoprotein, is an ecto-enzyme (ADP ribosyl cyclase/cADPR hydrolase/EC 3.2.2.6) that regulates cytoplasmic Ca2+ and cell-cell interactions. The molecule also delivers trans-membrane signals, despite a structural ineptitude to the scope. To reconcile these issues in a unitarian model, we compared the effects of CD38 signaling in circulating and residential T lymphocytes, the latter represented by those colonizing the intestinal lamina propria. Results are as follows: 1) LP T cells express an enzymatically active form of CD38, characterized by a modified ratio between cyclase and hydrolase functions; 2) LP T cells do not mobilize Ca2+ upon CD38 ligation, as seen in PB T cells (this condition is due to a lack in activation of PLC- g, constantly observed in PB T lymphocytes); 3) The early steps of CD38 signaling involve activation of lck, syk, and LAT; 4) Late events include synthesis and release of IL-2, IL-4, IL-5, IL-10, IFN-g and GM-CSF; 5) The uniqueness of the CD38 pathway in LP T cells is not caused by impaired interactions with the CD31 ligand. The differences observed concern the signaling machinery that CD38 exploits for its own use and not the interplay with its ligand.
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