TY - JOUR
T1 - Developmental expression of the type I diabetes related antigen sulfatide and sulfated lactosylceramide in mammalian pancreas
AU - Blomqvist, Maria
AU - Kaas, Anne
AU - Månsson, Jan-Eric
AU - Formby, Bent
AU - Rynmark, Britt-Marie
AU - Buschard, Karsten
AU - Fredman, Pam
N1 - Copyright 2003 Wiley-Liss, Inc.
PY - 2003/5/15
Y1 - 2003/5/15
N2 - Previous studies have shown that sulfatide is present and functionally involved in beta cells, and that anti-sulfatide antibodies (ASA) exist during development of type I diabetes mellitus. To further explore the possible role of sulfatide in type I diabetes, developmental expression was examined in human pancreas and in pancreas of the type I diabetes models BB rat and NOD mouse compared to Lewis rat and BALB/c mouse, respectively. Sulfatide was not only expressed in adult pancreas, but also in human fetal and rodent neonatal pancreas, i.e., during the growing period of the immunological self. Sulfatide had a different expression pattern in human beings and rodents, concerning both the amounts of sulfatide and expression during development. There was no change in the sulfatide fatty acid isoform expression during development. The pancreatic expression of another sulfated glycosphingolipid, sulfated lactosylceramide, indicated that this molecule is a potential fetal/neonatal marker, which was further expressed in the type I diabetic models. In conclusion, these findings give further support to the possibility that sulfatide is a relevant autoantigen in type I diabetes and that sulfated lactosylceramide might function as a potential risk factor for disease development, at least in the animal models.
AB - Previous studies have shown that sulfatide is present and functionally involved in beta cells, and that anti-sulfatide antibodies (ASA) exist during development of type I diabetes mellitus. To further explore the possible role of sulfatide in type I diabetes, developmental expression was examined in human pancreas and in pancreas of the type I diabetes models BB rat and NOD mouse compared to Lewis rat and BALB/c mouse, respectively. Sulfatide was not only expressed in adult pancreas, but also in human fetal and rodent neonatal pancreas, i.e., during the growing period of the immunological self. Sulfatide had a different expression pattern in human beings and rodents, concerning both the amounts of sulfatide and expression during development. There was no change in the sulfatide fatty acid isoform expression during development. The pancreatic expression of another sulfated glycosphingolipid, sulfated lactosylceramide, indicated that this molecule is a potential fetal/neonatal marker, which was further expressed in the type I diabetic models. In conclusion, these findings give further support to the possibility that sulfatide is a relevant autoantigen in type I diabetes and that sulfated lactosylceramide might function as a potential risk factor for disease development, at least in the animal models.
KW - Animals
KW - Antigens, CD/chemistry
KW - Chromatography, Thin Layer
KW - Diabetes Mellitus, Type 1/immunology
KW - Disease Models, Animal
KW - Humans
KW - Lactosylceramides/chemistry
KW - Mice
KW - Pancreas/embryology
KW - Rats
KW - Species Specificity
KW - Spectrometry, Mass, Electrospray Ionization
KW - Sulfoglycosphingolipids/immunology
U2 - 10.1002/jcb.10513
DO - 10.1002/jcb.10513
M3 - Journal article
C2 - 12704793
SN - 0730-2312
VL - 89
SP - 301
EP - 310
JO - Journal of Cellular Biochemistry
JF - Journal of Cellular Biochemistry
IS - 2
ER -