Cross-species compatibility of intercellular adhesion molecule-1 (CD54) with its ligands

Citation
An. Warrens et al., Cross-species compatibility of intercellular adhesion molecule-1 (CD54) with its ligands, TRANSPLANT, 69(3), 2000, pp. 394-399
Citations number
34
Categorie Soggetti
Medical Research Diagnosis & Treatment
Journal title
TRANSPLANTATION
ISSN journal
00411337 → ACNP
Volume
69
Issue
3
Year of publication
2000
Pages
394 - 399
Database
ISI
SICI code
0041-1337(20000215)69:3<394:CCOIAM>2.0.ZU;2-5
Abstract
Background The molecular interactions of intercellular adhesion molecule-1 (ICAM-1; CD54) are potentially important in several situations in the conte xt of pig-to-human xenotransplantation. If porcine bone marrow is to be use d for the induction of xenograft tolerance in humans, the role that has bee n suggested for ICAM-1 in the interactions of haematopoietic stem cells mak es its cross-species compatibility important. Similarly, the potential role of ICAM-1 interactions in graft rejection makes it an important molecule t o study. Methods, An in vitro static cell-to-cell adhesion study was used to look at the successful interaction of ICAM-1 with its ligands across the pig-human species barrier in both directions. A second in vitro system, the standard long-term bone marrow culture (LTBMC), was used to study the functional ro le of ICAM-1 in haematopoiesis. Results. Human ICAM-1 was able to adhere to ligands on porcine cells, inclu ding one or more ligand that contains CD18, Conversely, human CD18-containi ng ligands mediated adherence to porcine cells. Using the long-term bone ma rrow culture system, there was no evidence that blocking the interactions o f ICAM-1 inhibited hematopoiesis, either in the human-human or pig-human co mbinations of precursor cells and marrow stroma. Conclusions, ICAM-1 is able to interact with at least some of its ligands a cross the species barrier, in both pig-human and human-pig combinations. Ho wever, the interactions of ICAM-1 do not appear to be central to hematopoie sis, at least in the model system used.