Androgen/Wnt/β‐catenin signal axis augments cell proliferation of the mouse erectile tissue, corpus cavernosum. (29th March 2022)

• Record Type: Journal Article
• Authors: Kajimoto, Mizuki; Suzuki, Kentaro; Ueda, Yuko; Fujimoto, Kota; Takeo, Toru; Nakagata, Naomi; Hyuga, Taiju; Isono, Kyoichi; Yamada, Gen
• Is Part Of: Congenital anomalies. Volume 62:Number 3(2022)
• Page Start: 123
• Page End: 133
• Publication Date: 2022-03-29
• Subjects: androgen -- corpus cavernosum -- erectile tissue -- sexual differentiation -- Wnt/β‐catenin signaling; Abnormalities, Human -- Periodicals; 616.043
• DOI: 10.1111/cga.12465
• Languages: English
• ISSNs: 0914-3505

Abstract

Abstract: The murine penile erectile tissues including corpus cavernosum (CC) are composed of blood vessels, smooth muscle, and connective tissue, showing marked sexual differences. It has been known that the androgens are required for sexually dimorphic organogenesis. It is however unknown about the features of androgen signaling during mouse CC development. It is also unclear how androgen‐driven downstream factors are involved such processes. In the current study, we analyzed the onset of sexually dimorphic CC formation based on histological analyses, the dynamics of androgen receptor (AR) expression, and regulation of cell proliferation. Of note, we identified Dickkopf‐related protein 2 ( Dkk2 ), an inhibitor of β‐catenin signaling, was predominantly expressed in female CC compared with male. Furthermore, administration of androgens resulted in activation of β‐catenin signaling. We have found the Sox9 gene, one of the essential markers for chondrocyte, was specifically expressed in the developing CC. Hence, we utilized CC‐specific, Sox9 CreERT2, β‐catenin conditional mutant mice. Such mutant mice showed defective cell proliferation. Furthermore, introduction of activated form of β‐catenin mutation (gain of function mutation for Wnt/β‐catenin signaling) in CC induced augmented cell proliferation. Altogether, we revealed androgen‐Wnt/β‐catenin signal dependent cell proliferation was essential for sexually dimorphic CC formation. These findings open new avenues for understanding developmental mechanisms of androgen‐dependent cell proliferation during sexual differentiation.