Developmental expression of the type I diabetes related antigen sulfatide and sulfated lactosylceramide in mammalian pancreas

被引:11
作者
Blomqvist, M [1 ]
Kaas, A
Månsson, JE
Formby, B
Rynmark, BM
Buschard, K
Fredman, P
机构
[1] Univ Gothenburg, Inst Clin Neurosci, Expt Neurosci Sect, Sahlgrenska Acad,Sahlgrenska Univ Hosp, SE-43180 Molndal, Sweden
[2] Kommune Hosp Copenhagen, Bartholin Inst, DK-1399 Copenhagen K, Denmark
[3] Rasmus Inst Med Res, Santa Barbara, CA 93105 USA
关键词
sulfatide; sulfated lactosylceramide; glycosphingolipid; type I diabetes mellitus; animal model; fetal; neonatal;
D O I
10.1002/jcb.10513
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:301 / 310
页数:10
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