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Development of Human Adrenocortical Adenoma (HAA1) Cell Line from Zona Reticularis

Authors :
Hans K. Ghayee
Yiling Xu
Heather Hatch
Richard Brockway
Asha S. Multani
Tongjun Gu
Wendy B. Bollag
Adina Turcu
William E. Rainey
Juilee Rege
Kazutaka Nanba
Vikash J. Bhagwandin
Fiemu Nwariaku
Victor Stastny
Adi F. Gazdar
Jerry W. Shay
Richard J. Auchus
Sergei G. Tevosian
Source :
International Journal of Molecular Sciences, Vol 24, Iss 1, p 584 (2022)
Publication Year :
2022
Publisher :
MDPI AG, 2022.

Abstract

The human adrenal cortex is composed of distinct zones that are the main source of steroid hormone production. The mechanism of adrenocortical cell differentiation into several functionally organized populations with distinctive identities remains poorly understood. Human adrenal disease has been difficult to study, in part due to the absence of cultured cell lines that faithfully represent adrenal cell precursors in the early stages of transformation. Here, Human Adrenocortical Adenoma (HAA1) cell line derived from a patient’s macronodular adrenocortical hyperplasia and was treated with histone deacetylase inhibitors (HDACis) and gene expression was examined. We describe a patient-derived HAA1 cell line derived from the zona reticularis, the innermost zone of the adrenal cortex. The HAA1 cell line is unique in its ability to exit a latent state and respond with steroidogenic gene expression upon treatment with histone deacetylase inhibitors. The gene expression pattern of differentiated HAA1 cells partially recreates the roster of genes in the adrenal layer that they have been derived from. Gene ontology analysis of whole genome RNA-seq corroborated increased expression of steroidogenic genes upon HDAC inhibition. Surprisingly, HDACi treatment induced broad activation of the Tumor Necrosis Factor (TNF) alpha pathway. This novel cell line we developed will hopefully be instrumental in understanding the molecular and biochemical mechanisms controlling adrenocortical differentiation and steroidogenesis.

Details

Language :
English
ISSN :
14220067 and 16616596
Volume :
24
Issue :
1
Database :
Directory of Open Access Journals
Journal :
International Journal of Molecular Sciences
Publication Type :
Academic Journal
Accession number :
edsdoj.6db15ebcdfba404f90c05358b2a3b4b8
Document Type :
article
Full Text :
https://doi.org/10.3390/ijms24010584