PubMed Health⌕ Search

PubMed · 3533571

Chick embryonic erythrocyte antigen--tissues sharing expression.

Abstract

There is an antigenic glycoprotein (Mr 48 kD) present on the surfaces of erythrocytes of embryonic and young chickens that cannot be detected on the circulating erythrocytes in adult birds. This antigen, generally defined by this differential expression, has been thought to be associated with the maturation of hematopoietic tissues. We now present evidence, based on the use of a monoclonal antibody, maEE1, and the characteristic pattern of this glycoprotein on two-dimensional (2D) gels, that this antigen, which we have named chickEE, is expressed in a number of other embryonic and adult tissues. Immunofluorescent labeling of cryosections and flow-cytometric analysis of cells labeled with maEE1 have revealed the presence of chickEE in the retina (present in all layers), in muscle tissues (present in the endomysium and within the vascular endothelium), in the liver (especially evident on the lateral surface of hepatocytes and within the sinusoids), on epithelia such as the gut and kidney tubule epithelium and within lymphoid organs (present on bursacytes, splenocytes, thymocytes and peripheral leukocytes, and again within the endothelium) of young and adult animals. The 2D gel patterns of chickEE derived from embryonic tissues (retina, hind limb, thymus and bursa) and the adult tissues (retina and spleen) are very similar to that of the embryonic erythrocyte. Thus, the extended reactivity of the monoclonal antibody to chickEE, maEE1, with additional tissues is, in at least the tissues examined, based on the presence of the chickEE glycoprotein and not on incidental cross-reactivity. The evidence presented in this paper for the widely-shared expression of chickEE antigen makes it necessary to reconsider the function of this component of the cell surface.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

M M Miller, J R Pink. 1986. Chick embryonic erythrocyte antigen--tissues sharing expression.. https://doi.org/10.1016/0014-4827(86)90171-0

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↗