Related Experiment Video
Updated: Aug 17, 2026

Peptide-based Identification of Functional Motifs and their Binding Partners
Published on: June 30, 2013
Endogenous retroviral envelope peptide expression is involved in a regulation of lymphocyte and hematopoietic
I V Chernukhin1, S K Khaldoyanidi, K V Gaidul
1Institute of Clinical Immunology, Siberian Branch, Russian Academy of Medical Sciences, Novosibirsk.
Abstract:
A biological function of endogenously expressed MuLV p15E-related proteins for lymphocyte and hematopoietic precursor activity in mice was examined. A high level of endogenous p15E-related peptide expression in spleen cells of mice with hemolytic anemia rendered by phenylhydrazine (PHZ) treatment was observed, detected by hyperimmune rabbit antisera against amino acid sequence which compose the immunosuppressive domain (ISD) of exogenous viral transmembrane (TM) p15E protein. The conditioned medium of these cultured cells (PHZ/CM) was inhibitory for lymphocyte blastogenesis and granulocyte-macrophage (GM) precursor activity, but stimulatory for the erythroid colony growth. When added to PHZ/CM, anti-ISD/p15E antibodies were capable to abrogate these effects. These antibodies bound 14K and 48K structural peptides contented in PHZ/CM as presumably smaller components of env gene products. Given together, the results indicate that erythroid immature cells produce proteins appearing in cell culture medium which exert p15E-related properties. These peptides are suggested to exert a down regulation for both lymphocyte and GM precursor activities, and the colony-promoting effect towards erythroid compartment cells.
Insights
Endogenous MuLV p15E-related proteins in mice regulate hematopoietic stem cell activity. These peptides inhibit lymphocyte and granulocyte-macrophage precursors while stimulating erythroid colony growth.
Area of Science:
- Immunology
- Hematology
- Molecular Biology
Background:
- Endogenous retroviral proteins, such as MuLV p15E, play roles in cellular functions.
- The immunosuppressive domain (ISD) of MuLV p15E is known to affect immune responses.
- Hematopoietic precursor activity is crucial for blood cell formation and regulation.
Purpose of the Study:
- To investigate the biological function of endogenously expressed MuLV p15E-related proteins in mice.
- To determine the role of these proteins in lymphocyte and hematopoietic precursor activity.
- To examine the effects of phenylhydrazine (PHZ)-induced hemolytic anemia on p15E-related peptide expression.
Main Methods:
- Spleen cells from PHZ-treated mice were cultured.
- Hyperimmune rabbit antisera against the ISD of MuLV p15E were used for detection.
- Conditioned medium (PHZ/CM) was analyzed for its effects on lymphocyte blastogenesis and hematopoietic precursor activity.
- Antibodies against ISD/p15E were used to abrogate observed effects.
Main Results:
- High levels of endogenous p15E-related peptides were detected in spleen cells of PHZ-treated mice.
- PHZ/CM inhibited lymphocyte blastogenesis and granulocyte-macrophage (GM) precursor activity.
- PHZ/CM stimulated erythroid colony growth.
- Anti-ISD/p15E antibodies neutralized the effects of PHZ/CM.
- Antibodies bound to 14K and 48K structural peptides in PHZ/CM.
Conclusions:
- Erythroid immature cells produce and release p15E-related proteins into the cell culture medium.
- These endogenous peptides exhibit MuLV p15E-like properties, down-regulating lymphocyte and GM precursor activities.
- The identified peptides promote colony growth in the erythroid compartment, suggesting a regulatory role in hematopoiesis.
More Related Videos
Related Concept Videos
Retrovirus Life Cycles
Retroviruses
LTR Retrotransposons
The internal coding region of LTR retrotransposons and their mechanism of transposition closely resembles a...
Regulation of Nuclear Protein Sorting
Receptor Downregulation in MVBs
The EGFR can initiate signaling pathways that lead to cell proliferation, migration, and differentiation. Overexpression of EGFR stimulates cells to proliferate. Excessive EGFR activation may...
Regulation of Hematopoietic Stem Cells

