PubMed Health⌕ Search

PubMed · 1639632

HLA-DR expression in human fetal thymocytes.

Abstract

We analyzed the expression of MHC class I (W6/32) and class II (HLA-DR) antigens on human fetal and postnatal thymocytes by fluorescence-activated cell sorting. Less than 5% of prenatal thymocytes expressed HLA-DR before week 12 of gestation. However, the number of HLA-DR-positive cells significantly increased during the late second and third trimester of gestation, when greater than 50% of prenatal thymocytes expressed HLA-DR. Such high-level expressions of HLA-DR in fetal thymocytes were also demonstrated by Northern-blot analysis and immunohistochemistry. After birth, the percentage of HLA-DR-positive cells in thymocytes decreased gradually. A high-level expression of class I antigen was also observed in thymocytes from the early stages of gestation, but, in contrast to MHC class II, a majority of postnatal thymocytes maintained high levels of class I antigen after birth.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

S H Park, Y M Bae, T J Kim, I S Ha, S Kim, J G Chi, S K Lee. 1992. HLA-DR expression in human fetal thymocytes.. https://doi.org/10.1016/0198-8859(92)90338-n

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

KEEP EXPLORING

Related citations

Large dielectrophoresis force and torque induced by localized surface plasmon resonance of Au nanoparticle array.

A new approach is proposed for manipulating and rotating micro- or nano-objects by using polarized laser light with low intensity. The polarized light excites resonant dipoles on a cap-shaped Au nanoparticle array, which generates a highly nonuniform radiation field that induces large dielectrophoresis force on dielectric objects. The orientation control of the objects is realized by adjusting the polarization direction of the incident light. Theoretical modeling, fabrication, and characterization results for the cap-shaped Au nanoparticle array, as well as preliminary trapping results, are reported.

Cell Separation↗

[Cell tracking. Principles and applications].

Cell based therapies such as stem cell therapies or adoptive immunotherapies are currently being explored as a potential treatment for a variety of diseases such as Parkinson's disease, diabetes or cancer. However, quantitative and qualitative evaluation of adoptively transferred cells is indispensable for monitoring the efficiency of the treatment. Current approaches mostly analyze transferred cells from peripheral blood, which cannot assess whether transferred cells actually home to and stay in the targeted tissue. Using cell-labeling methods such as direct labeling or transfection with a marker gene in conjunction with various imaging modalities (MRI, optical or nuclear imaging), labeled cells can be followed in vivo in real-time, and their accumulation as well as function in vivo can be monitored and quantified accurately. This method is usually referred to as "cell tracking" or "cell trafficking" and is also being applied in basic biological sciences, exemplified in the evaluation of genes contributing to metastasis. This review focuses on principles of this promising methodology and explains various approaches by highlighting recent examples.

Cell Separation↗

[Molecular and parametric imaging with iron oxides].

Superparamagnetic iron oxide (SPIO) contrast agents, clinically established for high resolution magnetic resonance imaging of reticuloendothelial system containing anatomical structures, can additionally be exploited for the non-invasive characterization and quantification of pathology down to the molecular level. In this context, SPIOs can be applied for non-invasive cell tracking, quantification of tissue perfusion and target specific imaging, as well as for the detection of gene expression. This article provides an overview of new applications for clinically approved iron oxides as well of new, modified SPIO contrast agents for parametric and molecular imaging.

Cell Separation↗