Phagocytosis of Cholesteryl Ester Is Amplified in Diabetic Mouse Macrophages and Is Largely Mediated by CD36 and SR-A Cholesteryl Ester in MΦs
2007

Increased Cholesteryl Ester Uptake in Diabetic Mouse Macrophages

publication Evidence: moderate

Author Information

Author(s): Guest Christopher B., Hartman Matthew E., O'Connor Jason C., Chakour Kenneth S., Sovari Ali A., Freund Gregory G.

Primary Institution: University of Illinois at Urbana-Champaign

Hypothesis

Macrophages from type-2 diabetic (db/db) mice have increased direct cholesteryl ester uptake and that this is mediated by CD36 and SR-A.

Conclusion

Diabetic mouse macrophages show increased cholesteryl ester uptake due to higher expression of scavenger receptors CD36 and SR-A.

Supporting Evidence

  • Diabetic mice showed a 58% increase in cholesteryl ester accumulation compared to controls.
  • Blocking CD36 and SR-A reduced cholesteryl ester uptake by 37% and 25%, respectively.
  • Flow cytometry revealed a 43% increase in CD36 expression and an 80% increase in SR-A expression in diabetic macrophages.

Takeaway

Mice with diabetes have special cells that can take in more fat, which might make their hearts sick.

Methodology

The study involved administering cholesteryl esters to diabetic and control mice and measuring the uptake in peritoneal macrophages using flow cytometry.

Participant Demographics

The study used B6.Cg-M+/+Leprdb (db/+) and B6.Cg-+Leprdb/+Leprdb (db/db) mice.

Statistical Information

P-Value

p<0.01

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1371/journal.pone.0000511

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