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Let-7 and MicroRNA-148 Regulate Parathyroid Hormone Levels in Secondary Hyperparathyroidism
Vitali Shilo1, Irit Mor-Yosef Levi1, Roy Abel1
1Nephrology and Hypertension, Hadassah-Hebrew University Medical Center, Jerusalem, Israel; and.
Abstract:
Secondary hyperparathyroidism commonly complicates CKD and associates with morbidity and mortality. We profiled microRNA (miRNA) in parathyroid glands from experimental hyperparathyroidism models and patients receiving dialysis and studied the function of specific miRNAs. miRNA deep-sequencing showed that human and rodent parathyroids share similar profiles. Parathyroids from uremic and normal rats segregated on the basis of their miRNA expression profiles, and a similar finding was observed in humans. We identified parathyroid miRNAs that were dysregulated in experimental hyperparathyroidism, including miR-29, miR-21, miR-148, miR-30, and miR-141 (upregulated); and miR-10, miR-125, and miR-25 (downregulated). Inhibition of the abundant let-7 family increased parathyroid hormone (PTH) secretion in normal and uremic rats, as well as in mouse parathyroid organ cultures. Conversely, inhibition of the upregulated miR-148 family prevented the increase in serum PTH level in uremic rats and decreased levels of secreted PTH in parathyroid cultures. The evolutionary conservation of abundant miRNAs in normal parathyroid glands and the regulation of these miRNAs in secondary hyperparathyroidism indicates their importance for parathyroid function and the development of hyperparathyroidism. Specifically, let-7 and miR-148 antagonism modified PTH secretion in vivo and in vitro, implying roles for these specific miRNAs. These findings may be utilized for therapeutic interventions aimed at altering PTH expression in diseases such as osteoporosis and secondary hyperparathyroidism.
Insights
MicroRNAs (miRNAs) are dysregulated in secondary hyperparathyroidism. Targeting specific miRNAs like let-7 and miR-148 can modulate parathyroid hormone secretion, offering potential therapeutic strategies.
Area of Science:
- Endocrinology
- Molecular Biology
- Nephrology
Background:
- Secondary hyperparathyroidism is a common complication of chronic kidney disease (CKD), linked to increased morbidity and mortality.
- MicroRNA (miRNA) dysregulation is implicated in the pathogenesis of secondary hyperparathyroidism.
Purpose of the Study:
- To profile and functionally characterize miRNAs in parathyroid glands affected by experimental and human hyperparathyroidism.
- To investigate the role of specific miRNAs in regulating parathyroid hormone (PTH) secretion.
Main Methods:
- Deep-sequencing of miRNAs in parathyroid glands from experimental hyperparathyroidism models and human patients.
- Inhibition of specific miRNAs (let-7 family, miR-148 family) in vivo and in vitro to assess effects on PTH secretion.
Main Results:
- Parathyroid miRNA expression profiles differ between uremic and normal rats, with similar findings in humans.
- Several miRNAs, including miR-29, miR-21, miR-148, miR-30, miR-141, miR-10, miR-125, and miR-25, were found to be dysregulated in hyperparathyroidism.
- Inhibition of let-7 family miRNAs increased PTH secretion, while inhibition of miR-148 family miRNAs reduced PTH levels in vivo and in vitro.
Conclusions:
- Conserved miRNAs in parathyroid glands play crucial roles in regulating parathyroid function.
- Dysregulated miRNAs, particularly let-7 and miR-148, are critical in secondary hyperparathyroidism pathogenesis.
- Targeting specific miRNAs offers a potential therapeutic avenue for managing PTH levels in conditions like osteoporosis and CKD-related hyperparathyroidism.
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