Pcolce2 overexpression promotes supporting cell reprogramming in the neonatal mouse cochlea
Changling Xu , Liyan Zhang , Yinyi Zhou , Haoliang Du , Jieyu Qi , Fangzhi Tan , Li Peng , Xingliang Gu , Nianci Li , Qiuhan Sun , Ziyu Zhang , Yicheng Lu , Xiaoyun Qian , Busheng Tong , Jiaqiang Sun , Renjie Chai , Yi Shi
Cell Proliferation ›› 2024, Vol. 57 ›› Issue (8) : e13633
Pcolce2 overexpression promotes supporting cell reprogramming in the neonatal mouse cochlea
Hair cell (HC) damage is a leading cause of sensorineural hearing loss, and in mammals supporting cells (SCs) are unable to divide and regenerate HCs after birth spontaneously. Procollagen C-endopeptidase enhancer 2 (Pcolce2), which encodes a glycoprotein that acts as a functional procollagen C protease enhancer, was screened as a candidate regulator of SC plasticity in our previous study. In the current study, we used adeno-associated virus (AAV)-ie (a newly developed adeno-associated virus that targets SCs) to overexpress Pcolce2 in SCs. AAV-Pcolce2 facilitated SC re-entry into the cell cycle both in cultured cochlear organoids and in the postnatal cochlea. In the neomycin-damaged model, regenerated HCs were detected after overexpression of Pcolce2, and these were derived from SCs that had re-entered the cell cycle. These findings reveal that Pcolce2 may serve as a therapeutic target for the regeneration of HCs to treat hearing loss.
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2024 The Authors. Cell Proliferation published by Beijing Institute for Stem Cell and Regenerative Medicine and John Wiley & Sons Ltd.
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