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Published on: December 4, 2017
Extracellular matrix proteins Pericardin and Lonely heart mediate periostial hemocyte aggregation in the mosquito
Cole J Meier1, Shabbir Ahmed1, Jordyn S Barr1
1Department of Biological Sciences, Vanderbilt University, Nashville, TN, USA.
Insights
Cardiac extracellular matrix proteins, Pericardin (Prc) and Lonely heart (Loh), are crucial for directing immune cell (hemocyte) migration to the mosquito heart during infection. Their absence impairs this vital immune response.
Area of Science:
- Insect immunology
- Cardiovascular physiology
- Extracellular matrix biology
Background:
- Infections trigger hemocyte migration to insect hearts, where they aggregate at ostia to combat pathogens.
- The roles of cardiac extracellular matrix proteins in this immune cell aggregation are not well understood.
Purpose of the Study:
- To investigate if Pericardin (Prc) and Lonely heart (Loh) regulate infection-induced hemocyte aggregation at the mosquito heart.
- To determine the cardiac specificity of Prc and Loh function in immune responses.
Main Methods:
- RNA interference (RNAi) was used to silence Prc and Loh genes in An. gambiae mosquitoes.
- Hemocyte populations and distribution were analyzed in infected and uninfected mosquitoes.
- Melanin levels and infection intensity were assessed post-challenge.
Main Results:
- Silencing Prc or Loh reduced infection-induced hemocyte migration to the heart.
- These proteins did not affect resident hemocyte populations or their distribution in uninfected mosquitoes.
- Prc and Loh knockdown did not alter melanin production or early infection intensity, indicating a specific role in hemocyte trafficking.
Conclusions:
- Pericardin and Lonely heart are positive regulators of infection-induced hemocyte migration to the mosquito heart.
- Their function appears to be cardiac-specific, influencing immune cell trafficking rather than overall immune intensity or melanin production.
Abstract:
An infection induces the migration of immune cells called hemocytes to the insect heart, where they aggregate around heart valves called ostia and phagocytose pathogens in areas of high hemolymph flow. Here, we investigated whether the cardiac extracellular matrix proteins, Pericardin (Prc) and Lonely heart (Loh), regulate the infection-induced aggregation of periostial hemocytes in the mosquito, An. gambiae. We discovered that RNAi-based post-transcriptional silencing of Prc or Loh did not affect the resident population of periostial hemocytes in uninfected mosquitoes, but that knocking down these genes decreases the infection-induced migration of hemocytes to the heart. Knocking down Prc or Loh did not affect the proportional distribution of periostial hemocytes along the periostial regions. Moreover, knocking down Prc or Loh did not affect the number of sessile hemocytes outside the periostial regions, suggesting that the role of these proteins is cardiac-specific. Finally, knocking down Prc or Loh did not affect the amount of melanin at the periostial regions, or the intensity of an infection at 24 h after challenge. Overall, we demonstrate that Prc and Loh are positive regulators of the infection-induced migration of hemocytes to the heart of mosquitoes.
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