Related Experiment Video
Updated: May 15, 2026

Molecular Modulation by Lentivirus-Delivered Specific shRNAs in Endoplasmic Reticulum Stressed Neurons
Published on: April 24, 2021
Luman recruiting factor regulates endoplasmic reticulum stress in mouse ovarian granulosa cell apoptosis
Yanzhou Yang1, Pengfei Lin, Fenglei Chen
1Key Laboratory of Animal Biotechnology, Ministry of Agriculture, College of Veterinary Medicine, Northwest A&F University, Yangling, Shaanxi, PR China.
Abstract:
Follicular atresia is primarily induced by granulosa cell apoptosis; however, the molecular mechanisms that control apoptotic cell death in granulosa cells remain poorly understood. The present studies were undertaken to investigate the role of a novel endoplasmic reticulum stress-regulated gene Luman recruiting factor (LRF) in granulosa cell apoptosis during mouse follicular atresia. Based on immunohistochemistry and confocal laser scanning microscope analysis, LRF protein was localized in the cytoplasm of apoptotic granulosa cells, similar to localization of the LRF, Luman, CCAAT/enhancer-binding protein homologous protein and caspase-12 proteins were localized in apoptotic granulosa cells. However, glucose-regulated protein 78 protein was only present in healthy cells of the mural granulosa cell layers. A spontaneous onset of apoptotic cell death of granulosa cells was induced by thapsigargin or tunicamycin treatment in vitro, which was closely related to the increase of LRF, Luman, CCAAT/enhancer-binding protein homologous protein, and caspase-12 mRNA. Taken together, LRF might be involved in inducing apoptosis of granulosa cells through the endoplasmic reticulum stress pathway and might have a key role in mouse follicular selection.
Insights
Luman recruiting factor (LRF) induces granulosa cell apoptosis via endoplasmic reticulum stress, playing a key role in mouse follicular atresia and selection.
Area of Science:
- Reproductive Biology
- Cellular Biology
- Endocrinology
Background:
- Follicular atresia is driven by granulosa cell apoptosis, but its molecular triggers are unclear.
- Understanding granulosa cell apoptosis is crucial for reproductive health and fertility research.
Purpose of the Study:
- To investigate the role of Luman recruiting factor (LRF), an endoplasmic reticulum stress-responsive gene, in mouse follicular atresia.
- To elucidate the molecular mechanisms underlying granulosa cell apoptosis during follicular development.
Main Methods:
- Immunohistochemistry and confocal laser scanning microscopy to localize proteins in granulosa cells.
- In vitro induction of granulosa cell apoptosis using thapsigargin or tunicamycin.
- Quantitative analysis of gene expression (mRNA) for LRF and related proteins.
Main Results:
- LRF protein was detected in the cytoplasm of apoptotic granulosa cells.
- LRF, Luman, CCAAT/enhancer-binding protein homologous protein, and caspase-12 were upregulated during induced granulosa cell apoptosis.
- Glucose-regulated protein 78 was present only in healthy granulosa cells, suggesting a protective role.
Conclusions:
- LRF is implicated in inducing granulosa cell apoptosis through the endoplasmic reticulum stress pathway.
- LRF may play a critical role in the selection process of ovarian follicles in mice.
Related Concept Videos
Regulation of the Unfolded Protein Response
Role of ER in the Secretory Pathway
Components of the secretory pathway
About a third of proteins synthesized in the cell are sorted via the secretory route. They shuffle between different compartments in membrane-bound vesicles until they reach their final destination. The main intracellular compartments involved...
Feedback Regulation of Calcium Concentration
Various transmembrane receptors, such as G protein-coupled receptors (GPCRs), elicit a response to extracellular signals by increasing cytosolic calcium. Activated GPCRs...
The Unfolded Protein Response
Hormonal Regulation of the Menstrual Cycle
At puberty, GnRH begins a pulsatile release pattern, which triggers the anterior pituitary gland to secrete follicle-stimulating hormone (FSH) and luteinizing hormone (LH). The frequency and amplitude of GnRH pulses vary across the menstrual cycle, with faster pulses favoring LH release and slower pulses favoring FSH release.
Ovarian Cycle
