The activity of purine salvage pathway enzymes in murine and horse models of congenital and acquired dysimmunity.
Abstract: Previous studies of human congenital immunodeficiency states and in vitro observations of lymphocyte response to mitogens have implicated two purine salvage pathway enzymes, andenosine deaminase (ADA) and nucleoside phosphorylase (NP), as critical in the normal maturation and/or function of the immune system. Based on this information, ADA and NP activities were examined in a variety of congenital and acquired animal models of dysimmunity. The animals studied herein included: congenitally athymic (nude) mice; congenitally asplenic mice; congenitally athymic-asplenic mice; motheaten mice; New Zealand mice; and Arabian foals with severe combined immunodeficiency. No significant differences in the activities of ADA and NP were observed in any of these animals when compared with either normal littermates or animals with intact immune function. Major species differences were apparent when erythrocyte ADA acitivty was compared between mice and horses. In contrast, only minor strain alterations in ADA or NP activity were noted between several inbred groups of mice.
Publication Date: 1977-04-01 PubMed ID: 416973DOI: 10.1016/s0145-305x(77)80009-8Google Scholar: Lookup
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- Journal Article
- Research Support
- U.S. Gov't
- P.H.S.
Summary
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The research investigates the activity of two enzymes involved in the immune system’s normal functioning – Adenosine Deaminase (ADA) and Nucleoside Phosphorylase (NP) – in various congenital and acquired animal models of immune dysregulation. The study found no significant difference in these enzymes’ activities across these models, highlighting potential species variations in enzyme activity.
Research Background
- Adenosine Deaminase (ADA) and Nucleoside Phosphorylase (NP) are enzymes involved in the purine salvage pathway, a critical part of cellular metabolism.
- Prior research on human congenital immune deficiencies and lymphocyte responses suggests that these enzymes play a significant role in the immune system’s normal maturation and functionality.
Research Methodology
- The research examined ADA and NP activities in various congenital and acquired animal models of dysimmunity, which refers to conditions where the immune system fails to function adequately.
- The animal models used for this study included: congenitally athymic mice (lacking a thymus gland, important for immune system function); congenitally asplenic mice (born without a spleen); congenitally athymic-asplenic mice; motheaten mice; New Zealand mice; and Arabian foals with severe combined immunodeficiency.
Research Findings
- The researchers did not observe any significant differences in the activities of ADA and NP enzymes in the studied animals when compared to normal littermates or animals with normal immune function.
- There were significant species differences in erythrocyte ADA activity when comparing mice with horses. This finding suggests that there may be inherent variations in enzyme function attributable to species differences.
- However, minor variations in ADA or NP activity were observed between several inbred groups of mice, suggesting only minor strain alterations in these enzyme activities.
Implications
- These results contribute to the understanding of the role of ADA and NP enzymes in the immune function and might pave the way for new researches on how these enzymes function across different species.
- The lack of significant differences in enzyme activity amongst the studied models suggests that these enzymes may function consistently across different immune statuses. However, this pattern may vary across species, which warrants further investigation.
Cite This Article
APA
Castles JJ, Gershwin ME, Saito W, Ardans A, Osburn B.
(1977).
The activity of purine salvage pathway enzymes in murine and horse models of congenital and acquired dysimmunity.
Dev Comp Immunol, 1(2), 165-173.
https://doi.org/10.1016/s0145-305x(77)80009-8 Publication
Researcher Affiliations
MeSH Terms
- Adenosine Deaminase / blood
- Animals
- Disease Models, Animal
- Horses
- Immunologic Deficiency Syndromes / congenital
- Immunologic Deficiency Syndromes / immunology
- Mice
- Mice, Inbred BALB C
- Mice, Inbred CBA
- Mice, Inbred DBA
- Mice, Inbred NZB
- Mice, Nude
- Purine-Nucleoside Phosphorylase / blood
- Purines / metabolism
Citations
This article has been cited 3 times.- Crispens CG Jr. Adenosine deaminase activity in peripheral blood cells from SJL/J mice.. Experientia 1980 Oct 15;36(10):1220-1.
- Al-Safi SA, Maddocks JL. Azathioprine and 6-mercaptopurine (6-MP) suppress the human mixed lymphocyte reaction (MLR) by different mechanisms.. Br J Clin Pharmacol 1984 Apr;17(4):417-22.
- Magnuson NS, Perryman LE. In vitro of adenosine on lymphocytes and erythrocytes from horses with combined immunodeficiency.. J Clin Invest 1979 Jul;64(1):89-101.
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