Analysis of ROR1 Protein Expression in Mice with Reconstituted Human Immune System Components

被引:0
|
作者
Leung, Carol S. [1 ,2 ]
机构
[1] UCL, Canc Inst, Dept Hematol, London, England
[2] Univ Oxford, Ludwig Inst Canc Res, Nuffield Dept Med, Oxford, England
基金
瑞士国家科学基金会;
关键词
CHRONIC LYMPHOCYTIC-LEUKEMIA; HUMAN B; T-CELLS; HEMATOPOIETIC STEM; ANTIGEN ROR1; MOUSE MODEL; VIRUS; TCL1; RESPONSES; CANCER;
D O I
10.1155/2018/2480931
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Receptor tyrosine kinase-like orphan receptor 1 (ROR1) is an oncofetal antigen expressed on multiple tumors and has no significant expression on normal human tissues. ROR1 is highly upregulated in chronic lymphocytic leukemia (CLL) B cells. NOD-scid IL2rg(-/-) (NSG) mice engrafted with human CD34(+) hematopoietic progenitor cells (huNSG) achieved multilineage human immune cell reconstitution including B cells, T cells, NK cells, and DCs. Like the CLL patients, huNSG mice have abnormally high percentage of CD5-expressing B cells in the periphery. In light of this, we aim to determine whether ROR1 is expressed on huNSG B cells. Using flow cytometry analysis, we found that ROR1 was highly expressed in a proportion of bone marrow, spleen, and blood B cells, which were mostly immature B cells. Transplantation of the oncogene TCL-1-transduced CD34+ cells in neonatal NSG mice did not increase the frequency of ROR1-expressing B cells, but the mouse with the highest engraftment of transduced cells developed a tumor-like lump consisting of a high percentage of ROR1-expressing B cells. This study highlights the potential use of huNSG mice to study B cell malignant diseases and to evaluate immunotherapeutics targeting ROR1.
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页数:10
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