Ovarian Slice Culture

Ovarian slice culture is an ex vivo technique that maintains thin sections of ovarian tissue in controlled laboratory conditions, preserving tissue organization and interactions among follicles, oocytes, and supporting somatic cells. Nutrient-rich culture medium and regulated temperature and gas conditions support diffusion, cell viability, and continued developmental activity within the tissue while allowing direct observation and experimental manipulation. In developmental biology, this model helps researchers study folliculogenesis, oocyte growth, ovarian signaling, and the effects of genetic, hormonal, or environmental factors. Because it retains aspects of the native ovarian microenvironment, ovarian slice culture complements isolated-cell systems and can improve understanding of reproductive development.

Ovarian Slice Culture - Related Videos

Research

JoVE Journal - Developmental Biology
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Culture and Co-Culture of Mouse Ovaries and Ovarian Follicles

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Cited by 16 •

2015

This protocol describes the primary culture/co-culture of mouse ovarian tissue, using ovaries from neonatal mice and individual ovarian follicles from prepubertal mice. The culture techniques support development in a highly physiological manner, allowing investigation of the effect of extrinsic agents on the ovary, and of interactions between ovarian follicles.

Research

JoVE EoE - Gynecologic Cancer

Obtaining Primary Ovarian Cancer Cells from Solid Specimens: A Method to Culture Epithelial Ovarian Cancer Cells from Ovarian Tumor Specimens

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2023

In this video, we describe a method for isolating and characterizing primary ovarian cancer cells from solid ovarian tumor tissue specimens. The epithelial cancer cells obtained using this protocol are suitable for understanding the processes that may lead to ovarian cancer initiation and development.

Organotypic Hippocampal Slice Cultures

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Cited by 52 •

2011

We describe a method to prepare organotypic hippocampal slices that can be easily adapted to other brain regions. Brain slices are laid on porous membranes and culture media is allowed to form an interface. This method preserves the gross architecture of the hippocampus for up to 2 weeks in culture.

Modeling the Early Steps of Ovarian Cancer Dissemination in an Organotypic Culture of the Human Peritoneal Cavity

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Cited by 20 •

2015

Here, we present a protocol to construct a three-dimensional in vitro model of the lining of the peritoneal cavity, composed of primary human mesothelial cells and fibroblasts layered with extracellular matrix, as a tool to investigate ovarian cancer cell adhesion, invasion, and proliferation.

A Method for Ovarian Follicle Encapsulation and Culture in a Proteolytically Degradable 3 Dimensional System

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Cited by 80 •

2011

A new method for ovarian follicle encapsulation in a 3D fibrin-alginate interpenetrating network is described. This system combines structural support with proteolytic degradation to support the development of immature follicles to produce mature oocytes. This method may be applied to culture cell aggregates to maintain cell-cell contacts without limiting expansion.

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