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Updated: Aug 18, 2026

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Published on: May 17, 2015
Angiotensin-converting enzyme in macrophages and Freund's adjuvant granuloma
Abstract:
Low angiotensin-converting enzyme (ACE) activity was found in rat and mouse peritoneal macrophages, in rat and rabbit pulmonary alveolar macrophages, in cultured mouse peritoneal macrophages stimulated i.p. for four days by thioglycollate, and in rabbit pulmonary alveolar macrophages stimulated in culture by 0.1 to 100 microgram/ml Salmonella typhosa endotoxin for four days. Rat subcutaneous Freund's adjuvant granulomas induced with Mycobacterium butyricum or M. tuberculosis H37 Ra contianed low ACE activity which was generally lower than that present in control tissues. Increased ACE activity in sarcoidosis and Gaucher's disease lesions does not reflect a universally high synthesis of ACE in mammalian macrophages or granulomas, but may be due to specific mechanisms.
Insights
Angiotensin-converting enzyme (ACE) activity is generally low in macrophages and granulomas across multiple species. Specific mechanisms, not universal high synthesis, likely explain increased ACE in certain diseases.
Area of Science:
- Immunology
- Biochemistry
- Cell Biology
Background:
- Angiotensin-converting enzyme (ACE) plays a crucial role in the renin-angiotensin system.
- Macrophages are key immune cells involved in various physiological and pathological processes.
- Altered ACE activity in macrophages is implicated in certain disease states.
Purpose of the Study:
- To investigate the intrinsic angiotensin-converting enzyme (ACE) activity in macrophages and granulomas from different species.
- To determine if ACE activity is universally high in mammalian macrophages and granulomas.
- To explore factors influencing ACE activity in these cellular contexts.
Main Methods:
- Assessed ACE activity in peritoneal macrophages from rats and mice.
- Measured ACE activity in pulmonary alveolar macrophages from rats and rabbits.
- Quantified ACE activity in stimulated macrophages (thioglycollate, endotoxin) and granulomas (Freund's adjuvant).
Main Results:
- Low basal ACE activity was observed in rat and mouse peritoneal macrophages and rabbit pulmonary alveolar macrophages.
- Stimulated macrophages and granulomas (induced by thioglycollate, endotoxin, or mycobacteria) also exhibited low ACE activity.
- ACE activity in granulomas was generally lower than in control tissues.
Conclusions:
- Mammalian macrophages and granulomas generally possess low angiotensin-converting enzyme (ACE) activity.
- Increased ACE activity in diseases like sarcoidosis and Gaucher's disease is likely due to specific regulatory mechanisms, not widespread high ACE synthesis.
- Further research is needed to elucidate the specific mechanisms driving localized increases in ACE activity.
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