Granulosa cells affect in vitro maturation and subsequent parthenogenetic development of buffalo (Bubalus bubalis) oocytes. Issue 2 (11th June 2021)

• Record Type: Journal Article
• Authors: Zhang, Jun; Wang, Haoxin; Lu, Jiaka; Yu, Qing; Fu, Penghui; Li, Zhengda; Feng, Yun; Wang, Yanxin; Deng, Yanfei; Shi, Deshun; Lu, Fenghua
• Is Part Of: Reproduction in domestic animals. Volume 57:Issue 2(2022)
• Page Start: 141
• Page End: 148
• Publication Date: 2021-06-11
• Subjects: buffalo -- conditioned medium -- granulosa cells -- in vitro maturation -- monolayer -- oocytes; Animal breeding -- Periodicals; Veterinary pathology -- Periodicals; Livestock -- Breeding -- Periodicals; 636.082
• DOI: 10.1111/rda.13974
• Languages: English
• ISSNs: 0936-6768

Abstract

Abstract: Granulosa cells (GCs) play a crucial role in follicular development and atresia. Previous studies have showed that GCs in the form of monolayer influenced in vitro maturation (IVM) of oocytes. However, the effects of GCs in the form of conditioned medium and monolayer on IVM and development competence of buffalo oocytes remain unclear. In the present study, we examined the impacts of GC‐conditioned medium (GCCM) and monolayer GC on maturation efficiency and embryo development of buffalo oocytes after parthenogenetic activation (PA). Our results showed that GCCM that was collected on day 2 and added to IVM medium at a 20% proportional level (2 days and 20%) exerted significant negative effects on IVM rate (41.6% vs. 44.5%), but significantly enhanced embryo development (oocyte cleavage, 81.3% vs. 69.3%; blastocyst formation, 36.3% vs. 29.3%) of buffalo oocytes after PA compared with the control group. Furthermore, monolayer GC significantly reduced both maturation efficiency (40.2% vs. 44.5%) and embryo development (oocyte cleavage, 60.6% vs. 69.3%; blastocyst formation, 20.6% vs. 29.3%) of buffalo oocytes after PA compared to the control group. Our study indicated that GCs in the form of GCCM (2 days and 20%) and monolayer GC had different effects on IVM and subsequent parthenogenetic development of buffalo oocytes.