Multi‐Scale Ice Inhibition Platform Enables Full‐Cycle Cryogenic Protection for Mouse Oocyte

Author:

Chang Tie1,Tian Conghui1,Zheng Yifan2,Yang Yating3,Liu Tao4,Chen Zhongrong5,Shao Yue2,Shi Qinghua4,Liu Huanzhong3,Cao Yunxia678,Zhao Gang18ORCID

Affiliation:

1. Department of Electronic Engineering and Information Science University of Science and Technology of China Hefei 230027 China

2. Institute of Biomechanics and Medical Engineering Department of Engineering Mechanics School of Aerospace Engineering Tsinghua University Beijing 100084 China

3. Department of Psychiatry Chaohu Hospital of Anhui Medical University Hefei 230032 China

4. Division of Reproduction and Genetics First Affiliated Hospital of USTC Hefei National Laboratory for Physical Science at Microscale the CAS Key Laboratory of Innate Immunity and Chronic Disease School of Basic Medical Sciences Division of Life Sciences and Medicine Biomedical Sciences and Health Laboratory of Anhui Province CAS Center for Excellence in Molecular Cell Scienc Collaborative Innovation Center of Genetics and Development University of Science and Technology of China Hefei 230027 China

5. School of Biomedical Engineering Anhui Medical University Hefei 230032 China

6. Reproductive Medicine Center Department of Obstetrics and Gynecology the First Affiliated Hospital of Anhui Medical University Hefei 230032 China

7. NHC Key Laboratory of Study on Abnormal Gametes and Reproductive Tract (Anhui Medical University) Hefei 230032 China

8. Engineering Research Center of Biopreservation and Artificial Organs Ministry of Education Hefei 230032 China

Abstract

AbstractCryopreservation of metaphase II (MII) oocytes is crucial to preserve female fertility. However, the existing vitrification technology just provides partial cryogenic protection for oocytes and must use high concentrations of toxic penetrating cryoprotective agents (CPAs, up to 4.8 M). Here, a multi‐scale ice inhibition platform is proposed, which effectively suppresses ice crystal morphology, ice recrystallization (IR), temperature gradient, and devitrification. This platform achieves mouse oocyte survival rate of 98.6% using the low concentration of CPA (3.1 M) while also possessing batch oocyte cryopreservation ability. In contrast, recovered oocytes show a much more modest variation of genes compared with the conventional method (85 vs. 1396 genes), retaining normal fertilization, embryonic development, and birth to healthy offspring. Diverging from the conventional vitrification method with partial cryogenic protection capability, this platform introduces full‐cycle ice inhibition, offering promising prospects for achieving high‐quality and scalable fertility preservation.

Funder

National Natural Science Foundation of China

National Key Research and Development Program of China

Publisher

Wiley

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