PubMed Health⌕ Search

PubMed · 3703801

Bursal development in normal and testosterone-treated chick embryos.

Abstract

The development of the bursa of Fabricius was studied in normal and testosterone-treated embryos. The bursal anlage appears on the 5th day of incubation as an outgrowth of the dorso-caudal wall of the cloaca. By Day 7, the bursal lumen is present and separated from the anal invagination by a thin epithelial membrane. Shortly after this developmental state, the epithelial membrane disappears and the bursal lumen freely communicates with the amniotic cavity. The remnant of the bursal anlage forms the ventral wall of the anal invagination that is actually the bursal duct. Disappearance of the remnant of the bursal anlage, which takes place after the 16th day of incubation, allows the bursa to join the cloaca. Bursal folds appear on the 10th day of incubation. Mesenchymal cells then differentiate into dark and light cells. The dark cells, between 11 and 14 days of incubation, mobilize in the mesenchymal network and assemble in small groups under the epithelial rudiment of the folds. They, then, enter the epithelium where they induce bud formation. During the assemblage of dark cells beneath the epithelium and their emigration into the epithelium, they acquire cytoplasmic granules that resemble avian secretory cells. The light cells do not associate with the epithelium. They may be the precursors of cortical reticular cells. The differentiation of dark cells is inhibited in the presence of testosterone. Therefore, the failure of bud formation and subsequent follicular formation in the bursa of testosterone-treated embryos may be attributed to the elimination of an induction signal supplied by the differentiated dark cells of the mesenchyme.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

I Oláh, B Glick, I Törö. 1986. Bursal development in normal and testosterone-treated chick embryos.. https://doi.org/10.3382/ps.0650574

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Protocol for Detecting and Sequencing Chikungunya Virus from Field-Collected Mosquitoes.

Arboviral diseases represent a major public health challenge, especially in tropical regions where environmental conditions may favor the proliferation and spread of mosquito vectors. Thus, early and accurate detection of chikungunya virus (CHIKV) in mosquito populations can be a valuable tool for effective surveillance of circulating variants and for identifying new viral introductions. Given the challenges of detecting arboviruses in field-captured mosquitoes, we describe an integrated workflow for CHIKV molecular detection and whole-genome sequencing. This protocol includes mosquito homogenization using a bead-based mechanical disruptor, RNA extraction using TRIzol reagent with minor modifications, molecular screening using CHIKV-specific RT-qPCR, and whole-genome amplification followed by sequencing on Illumina platforms. Despite the protocol being optimized for individual mosquitoes, it results in high-quality RNA suitable for both entomological surveillance and genomic analysis. As this protocol allows recovery of complete CHIKV genomes from mosquito specimens, it can serve as a basis for genomic epidemiology studies, enabling monitoring of viral diversity and lineage dynamics, and facilitating early detection of emerging variants to support timely and targeted public health interventions in endemic and at-risk regions.

Animals↗

Genomic Profiling of Chromatin State Using CUT&Tag.

Alterations in chromatin state, mediated through histone modifications and the incorporation of histone variants, are fundamental to establishing transcriptional networks and cell identity. Recent advances in low-input epigenome profiling methods, such as CUT&Tag and CUT&RUN, have enabled the study of chromatin states from very limited starting materials. In this chapter, we describe procedures for generating CUT&Tag libraries to profile histone modifications and histone variants in early-developing zebrafish embryos.

Animals↗

Relaxin-2: Shaping the Proteomic Landscape of Skeletal Muscle Physiology, Glucose Trafficking, and Mitochondrial Function in Rat.

Relaxin-2 is a hormone with robust beneficial effects on the heart and blood vessels and potential as a therapy for cardiovascular (CV) disease. Considering the interorgan communication between skeletal muscle and heart, and the relation between muscle quality/composition and CV events, we hypothesize that relaxin-2 may regulate skeletal muscle physiology and metabolism. We aim to evaluate the impact of relaxin-2 on the proteome of skeletal muscle from healthy Sprague-Dawley rats. Animals were treated with 0.4 mg/kg/day of serelaxin (recombinant form of human relaxin-2) or vehicle (PBS) for 2 weeks employing subcutaneous osmotic minipumps. Skeletal muscle protein identification and quantification were performed by LC-MS/MS using a Data-Independent Acquisition (DIA)-Sequential Window Acquisition of All Theoretical Fragment Ion Spectra (SWATH) method. SWATH/MS quantitative analysis identified that relaxin-2 significantly decreased 95 proteins and significantly increased 32 proteins in rat skeletal muscle when compared to control rats. From these, 34 proteins were associated with muscle function, myogenesis, muscle differentiation and/or regeneration, 20 are mitochondrial proteins (six from the complexes of the electron transport chain), and 10 proteins participate in glucose metabolism. Qualitative data-dependent workflow analysis identified 35 proteins exclusive to the skeletal muscle of the relaxin-2-treated group: eight proteins related to processes of skeletal muscle function (size, ion homeostasis or organization of caveolae structures and cytoskeleton) and myogenesis, and two proteins involved in muscle differentiation. Our work highlighted for the first time the role of relaxin-2 in crucial processes of muscle physiology and energetic metabolism, which could influence several processes involved in myopathy and CV.

Animals↗