Abstract

The adrenal medulla is composed predominantly of chromaffin cells producing and secreting the catecholamines dopamine, norepinephrine, and epinephrine. Catecholamine biosynthesis and secretion is a complex and tightly controlled physiologic process. The pathways involved have been extensively studied, and various elements of the underlying molecular machinery have been identified. In this review, we provide a detailed description of the route from stimulus to secretion of catecholamines by the normal adrenal chromaffin cell compared to chromaffin tumor cells in pheochromocytomas. Pheochromocytomas are adrenomedullary tumors that are characterized by uncontrolled synthesis and secretion of catecholamines. This uncontrolled secretion can be partly explained by perturbations of the molecular catecholamine secretory machinery in pheochromocytoma cells. Chromaffin cell tumors also include sympathetic paragangliomas originating in sympathetic ganglia. Pheochromocytomas and paragangliomas are usually locally confined tumors, but about 15% do metastasize to distant locations. Histopathological examination currently poorly predicts future biologic behavior, thus long term postoperative follow-up is required. Therefore, there is an unmet need for prognostic biomarkers. Clearer understanding of the cellular mechanisms involved in the secretory characteristics of pheochromocytomas and sympathetic paragangliomas may offer one approach for the discovery of novel prognostic biomarkers for improved therapeutic targeting and monitoring of treatment or disease progression.

Highlights

  • The adrenal medulla occupies the central portion of the adrenal gland and accounts for about 10%of total adrenal gland volume [1]

  • We aim to provide a detailed picture of the pathways involved in catecholamine production and secretion in normal adrenomedullary chromaffin cells

  • Catecholamine biosynthesis involves the sequential activity of four enzymes: tyrosine hydroxylase (TH), aromatic L-amino acid decarboxylase (AADC), dopamine β-hydroxylase (DBH), and phenylethanolamine-N-methyltransferase (PNMT)

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Summary

Introduction

The adrenal medulla occupies the central portion of the adrenal gland and accounts for about 10%. The principal function of the adrenal medulla is the biosynthesis and the secretion into the circulation of the catecholamine epinephrine [6,11]. Epinephrine functions as a circulating metabolic hormone, and it is the norepinephrine secreted by sympathetic nerves acting immediately in the vicinity of exocytotic secretion that is the catecholamine mainly regulating cardiovascular function. We visit what is known about the molecular perturbations in catecholamine biosynthesis and secretion in pheochromocytoma and sympathetic paraganglioma. Improved understanding of these mechanisms at the molecular level might provide insight into associated pathological complications, clarify highly variable presentations, and aid in identification of new diagnostic or therapeutic strategies for personalized care

Biosynthesis of Catecholamines
Tyrosine Hydroxylase
Aromatic L-Amino Acid Decarboxylase
Dopamine β-hydroxylase
Phenylethanolamine-N-Methyltransferase
Co-Secreted Products
Storage and Vesicular Transmembrane Dynamics
Characteristics of Chromaffin Storage Vesicles
Secretion and Re-Uptake of Catecholamines
Stimulus-Dependent Exocytosis in Adrenal Chromaffin Cells
Neuronal Regulation of the Calcium-Dependent Catecholamine Secretory Pathway
Non-Neuronal Regulation of Catecholamine Secretion
Pheochromocytoma and Paraganglioma
Increased Biosynthesis of Catecholamines
Relationship between Genotype and Catecholamine Biochemical Phenotype
Relationship between Genotype and Catecholamine Secretory Pathways
Clinical Features and Risk Factors
Findings
Conclusions and Future Perspectives
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