The developmental origin and the specification of the adrenal cortex in humans and cynomolgus monkeys

Author:

Cheng Keren12ORCID,Seita Yasunari123ORCID,Moriwaki Taku12ORCID,Noshiro Kiwamu4,Sakata Yuka12,Hwang Young Sun12ORCID,Torigoe Toshihiko5ORCID,Saitou Mitinori678ORCID,Tsuchiya Hideaki9,Iwatani Chizuru9,Hosaka Masayoshi10,Ohkouchi Toshihiro11,Watari Hidemichi4,Umazume Takeshi4ORCID,Sasaki Kotaro12ORCID

Affiliation:

1. Institute for Regenerative Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

2. Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

3. Bell Research Center for Reproductive Health and Cancer, Nagoya 460-0003, Japan.

4. Department of Obstetrics and Gynecology, Hokkaido University Graduate School of Medicine, Sapporo 060-8638, Japan.

5. Department of Pathology, Sapporo Medical University Graduate School of Medicine, Sapporo 060-8556, Japan.

6. Department of Anatomy and Cell Biology, Graduate School of Medicine, Kyoto University, Kyoto 606-8501, Japan.

7. Institute for the Advanced Study of Human Biology (ASHBi), Kyoto University, Kyoto 606-8501, Japan.

8. Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto 606-8507, Japan.

9. Research Center for Animal Life Science, Shiga University of Medical Science, Otsu 520-2192, Japan.

10. Fukuzumi Obstetrics and Gynecology Hospital, Sapporo 062-0043, Japan.

11. Ohkouchi Obstetrics and Gynecology Hospital, Sapporo 060-0062, Japan.

Abstract

Development of the adrenal cortex, a vital endocrine organ, originates in the adrenogonadal primordium, a common progenitor for both the adrenocortical and gonadal lineages in rodents. In contrast, we find that in humans and cynomolgus monkeys, the adrenocortical lineage originates in a temporally and spatially distinct fashion from the gonadal lineage, arising earlier and more anteriorly within the coelomic epithelium. The adrenal primordium arises from adrenogenic coelomic epithelium via an epithelial-to-mesenchymal transition, which then progresses into the steroidogenic fetal zone via both direct and indirect routes. Notably, we find that adrenocortical and gonadal lineages exhibit distinct HOX codes, suggesting distinct anterior-posterior regionalization. Together, our assessment of the early divergence of these lineages provides a molecular framework for understanding human adrenal and gonadal disorders.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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