Proinsulin is encoded by an RNA splice variant in human blood myeloid cells


Autoria(s): Narendran, Parth; Neale, Alana M.; Lee, Bo Han; Ngui, Katrina; Steptoe, Raymond J.; Morahan, Grant; Madsen, Ole; Dromey, James A.; Jensen, Kent P.; Harrison, Leonard C.
Data(s)

01/01/2006

Resumo

Genes for peripheral tissue-restricted self-antigens are expressed in thymic and hematopoietic cells. In thymic medullary epithelial cells, self-antigen expression imposes selection on developing autoreactive T cells and regulates susceptibility to autoimmune disease in mouse models. Less is known about the role of self-antigen expression by hematopoietic cells. Here we demonstrate that one of the endocrine self-antigens expressed by human blood myeloid cells, proinsulin, is encoded by an RNA splice variant. The surface expression of immunoreactive proinsulin was significantly decreased after transfection of monocytes with small interfering RNA to proinsulin. Furthermore, analogous to proinsulin transcripts in the thymus, the abundance of the proinsulin RNA splice variant in blood cells corresponded with the length of the variable number of tandem repeats 5' of the proinsulin gene, known to be associated with type 1 diabetes susceptibility. Self-antigen expression by peripheral myeloid cells extends the umbrella of immunological self and, by analogy with the thymus, may be implicated in peripheral immune tolerance.

Identificador

http://espace.library.uq.edu.au/view/UQ:82971

Idioma(s)

eng

Publicador

National Academy of Sciences

Palavras-Chave #Immunology #Variable number of tandem repeats #Insulin #Type 1 diabetes #siRNA #Self-antigen #CX #320202 Cellular Immunology #730102 Immune system and allergy
Tipo

Journal Article