Pattern of expression of ecotropic murine leukemia virus in gonads of inoculated SWR/J mice.

J Virol

Unité de Génétique Cellulaire, Collège de France, Paris.

Published: May 1989

An ecotropic murine leukemia virus (MuLV) isolate has recently been shown to be able to infect the germ line or the early embryo or both when inoculated at birth to SWR/J females (J. J. Panthier, H. Condamine, and F. Jacob, Proc. Natl. Acad. Sci. USA 85:1156-1160, 1988). We have used this isolate to further study this phenomenon. By using the techniques of RNA-RNA in situ hybridization, immunocytochemistry, and transmission electron microscopy, the identities of two important cell types that are infected by ecotropic MuLV in the gonads of inoculated mice were determined. These cells are the thecal cells surrounding the follicles in the ovary and the Leydig cells in the testis. Both types actively synthesize viral RNA and express a viral antigen. Furthermore, we documented the production of viral particles by the thecal cells. The expression of ecotropic MuLV by nonlymphoid cells in vivo may play a key role in the vertical transmission of these viruses by females as well as in their horizontal transmission.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC250630PMC
http://dx.doi.org/10.1128/JVI.63.5.2134-2142.1989DOI Listing

Publication Analysis

Top Keywords

expression ecotropic
8
ecotropic murine
8
murine leukemia
8
leukemia virus
8
gonads inoculated
8
ecotropic mulv
8
thecal cells
8
cells
5
pattern expression
4
ecotropic
4

Similar Publications

MLL1 promotes placental trophoblast ferroptosis and aggravates preeclampsia symptoms through epigenetic regulation of RBM15/TRIM72/ADAM9 axis.

Biol Direct

December 2024

Department of Gynaecology and Obstetrics, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, No. 32, West Second Section, 1st Ring Road, Qingyang District, Chengdu, 610072, Sichuan Province, China.

Article Synopsis
  • This study investigates how MLL1 influences trophoblast ferroptosis in preeclampsia (PE) through epigenetic mechanisms, using both murine models and in vitro cell tests.
  • Key findings reveal that MLL1 is highly expressed in the placental tissues of PE mice, and inhibiting MLL1 can alleviate PE symptoms and reduce ferroptosis.
  • The research highlights a regulatory pathway involving MLL1, RBM15, TRIM72, and ADAM9, where MLL1 enhances RBM15 expression, which in turn influences TRIM72 mRNA stability and its interaction with ADAM9, leading to the degradation of ADAM9.
View Article and Find Full Text PDF

Evi1 governs Kdm6b-mediated histone demethylation to regulate the Laptm4b-driven mTOR pathway in hematopoietic progenitor cells.

J Clin Invest

December 2024

Department of Medicine and Department of Biochemistry and Molecular Biology, UF Health Cancer Center, University of Florida, Gainesville, Florida, USA.

Ecotropic viral integration site 1 (EVI1/MECOM) is frequently upregulated in myeloid malignancies. Here, we present an Evi1-transgenic mouse model with inducible expression in hematopoietic stem/progenitor cells (HSPCs). Upon induction of Evi1 expression, mice displayed anemia, thrombocytopenia, lymphopenia, and erythroid and megakaryocyte dysplasia with a significant expansion of committed myeloid progenitor cells, resembling human myelodysplastic syndrome/myeloproliferative neoplasm-like (MDS/MPN-like) disease.

View Article and Find Full Text PDF

Clinical significance of dynamic monitoring of EVI1 gene expression in pediatric acute myeloid leukemia.

BMC Pediatr

December 2024

Department of Hematology, Children's Medical Institute of Hematology, Wuhan Children's Hospital, Tongji Medical College, Huazhong University of Science & Technology, Wuhan, 430016, China.

Objective: To investigate the clinical significance of dynamic monitoring ecotropic virus integration site-1 (EVI1) expression in childhood acute myeloid leukemia (AML).

Methods: A retrospective analysis was conducted on 113 pediatric AML patients of Wuhan Children's Hospital from 2014 to 2022. The correlation between EVI1 expression levels and clinical indicators including clinical characteristics, first complete remission (CR1), relapse, and overall survival (OS) was analyzed.

View Article and Find Full Text PDF

Microcell-mediated chromosome transfer between non-identical human iPSCs.

Mol Ther Nucleic Acids

December 2024

Department of Chromosome Biomedical Engineering, Integrated Medical Sciences, Graduate School of Medical Sciences, Tottori University, 86 Nishi-cho, Yonago, Tottori 683-8503, Japan.

Article Synopsis
  • Microcell-mediated chromosome transfer (MMCT) is a new technique for manipulating chromosome numbers using human induced pluripotent stem cells (hiPSCs) to create disease models with hyperaneuploidy.
  • The study highlights the efficiency of using hiPSCs as both donor and recipient cells in the chromosome transfer process, allowing for the tagging and transfer of specific chromosomes like Chr21 and ChrY using CRISPR-Cas9.
  • This innovative method aims to improve the study of rare diseases and enhance our understanding of early development by integrating key chromosomal regions into hiPSCs.
View Article and Find Full Text PDF
Article Synopsis
  • MEIS1 and MEIS2 are important genes that code for proteins involved in development across various tissues, particularly in the brain, but their specific roles in early neural differentiation need further investigation.
  • Research involving knockout and overexpression of these genes in human neural stem cells reveals that MEIS1 and MEIS2 regulate different groups of target genes linked to various biological functions.
  • MEIS1 is not only connected to gene regulation, especially in relation to other transcription factors, but it also has a significant risk factor for restless legs syndrome (RLS), as it controls genes associated with this condition.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!