Book contents
- Frontmatter
- Dedication
- Contents
- List of Contributors
- Preface
- Section 1 Historical perspective
- Section 2 Life cycle
- Section 3 Developmental biology
- 8 Structural basis for oocyte–granulosa cell interactions
- 9 Differential gene expression mediated by oocyte–granulosa cell communication
- 10 Hormones and growth factors in the regulation of oocyte maturation
- 11 Getting into and out of oocyte maturation
- 12 Chromosome behavior and spindle formation in mammalian oocytes
- 13 Transcription, accumulation, storage, recruitment, and degradation of maternal mRNA in mammalian oocytes
- 14 Setting the stage for fertilization: transcriptome and maternal factors
- 15 Egg activation: initiation and decoding of Ca2+ signaling
- 16 In vitro growth and differentiation of oocytes
- 17 Metabolism of the follicle and oocyte in vivo and in vitro
- 18 Improving oocyte maturation in vitro
- Section 4 Imprinting and reprogramming
- Section 5 Pathology
- Section 6 Technology and clinical medicine
- Index
- References
8 - Structural basis for oocyte–granulosa cell interactions
from Section 3 - Developmental biology
Published online by Cambridge University Press: 05 October 2013
- Frontmatter
- Dedication
- Contents
- List of Contributors
- Preface
- Section 1 Historical perspective
- Section 2 Life cycle
- Section 3 Developmental biology
- 8 Structural basis for oocyte–granulosa cell interactions
- 9 Differential gene expression mediated by oocyte–granulosa cell communication
- 10 Hormones and growth factors in the regulation of oocyte maturation
- 11 Getting into and out of oocyte maturation
- 12 Chromosome behavior and spindle formation in mammalian oocytes
- 13 Transcription, accumulation, storage, recruitment, and degradation of maternal mRNA in mammalian oocytes
- 14 Setting the stage for fertilization: transcriptome and maternal factors
- 15 Egg activation: initiation and decoding of Ca2+ signaling
- 16 In vitro growth and differentiation of oocytes
- 17 Metabolism of the follicle and oocyte in vivo and in vitro
- 18 Improving oocyte maturation in vitro
- Section 4 Imprinting and reprogramming
- Section 5 Pathology
- Section 6 Technology and clinical medicine
- Index
- References
Summary
Introduction
Cellular interactions are known to be essential not only in mammalian developing tissues and organs, but also during steady-state maintenance phases. In the mammalian ovary, cellular interactions are particularly important since follicle development is continuously initiated, during childhood and adulthood, until the follicle pool drops below a poorly understood threshold in menopause. In this context, the germ cell–soma interface is of major relevance since it is at this level that a fine tuning must take place to allow for correct ovarian follicle development and the full oocyte functionality, known as oocyte competence acquisition. This includes complex differentiation processes of the somatic cells, fine tuning in response to growth factors and hormones, and the regulation of meiotic arrest and metabolism to the demand of the growing and maturing oocyte.
Although the zona pellucida, an oocyte-specific extracellular layer, intercalates between oocytes and the innermost layer of cumulus granulosa cells (corona radiata), unique cellular structures are present at this level that emanate from the granulosa cell, extend across the zona pellucida, and reach direct contact with the oocyte's plasma membrane. These structures, known as the transzonal projections (TZPs), may contain cytoskeletal components, such as tubulin and/or actin, and possess membrane junctions such as gap and adhesion junctions, and cell organelles such as mitochondria. Between neighboring granulosa cells similar specialized junctions exist that allow direct cell–cell signaling but also permit nutrient access to the oocyte.
- Type
- Chapter
- Information
- Biology and Pathology of the OocyteRole in Fertility, Medicine and Nuclear Reprograming, pp. 81 - 98Publisher: Cambridge University PressPrint publication year: 2013