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Differences in Immune Cell-Derived Circular RNA Between Fulminant Type 1 Diabetes and Type 1 Diabetes
Wenfeng Yin1, Shuoming Luo1, Junlin Qiu1
1Department of Metabolism and Endocrinology, National Clinical Research Center for Metabolic Diseases, Key Laboratory of Diabetes Immunology (Central South University), Ministry of Education, The Second Xiangya Hospital of Central South University, Changsha, China.
This study identified distinct circular RNA profiles in peripheral blood mononuclear cells from patients with fulminant type 1 diabetes (FT1D) and type 1 diabetes (T1D). These findings reveal novel molecular mechanisms differentiating FT1D from T1D.
Area of Science:
- Endocrinology and Metabolism
- Molecular Biology
- Immunology
Background:
- Circular RNAs (circRNAs) are implicated in type 1 diabetes (T1D) pathogenesis.
- Specific circRNA differences between fulminant type 1 diabetes (FT1D) and T1D are not well understood.
Purpose of the Study:
- To identify and characterize circRNAs in peripheral blood mononuclear cells (PBMCs) from FT1D and T1D patients.
- To explore the functional roles and molecular networks of these differentially expressed circRNAs.
Main Methods:
- PBMCs were isolated from FT1D and T1D patients.
- circRNA expression profiling was performed using the Arraystar Human circRNA Array.
- RT-qPCR validated key circRNAs in an independent cohort.
- Bioinformatics analyses predicted circRNA functions and networks.
Main Results:
- 145 differentially expressed circRNAs were identified between FT1D and T1D.
- Hsa_circRNA_038288, hsa_circRNA_104405, and hsa_circRNA_405498 were validated.
- Parent genes were enriched in RNA transport, ubiquitin-mediated proteolysis, and focal adhesion pathways.
- Hsa_circRNA_038288 showed potential coding capacity and involvement in immune regulation and diabetes progression.
Conclusions:
- Significant differences in immune cell-derived circRNAs distinguish FT1D from T1D.
- These findings provide new insights into the distinct molecular mechanisms underlying FT1D and T1D.
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