Summary
Haemocytes from the ascidianBotrylloides leachii were observed in vivo to phagocytose sheep erythrocytes. The possibility that a sheep erythrocyte agglutinin (the HA-2 agglutinin) previously purified fromB. leachii haemolymph functions as a recognition molecule for the phagocytosis of these erythrocytes was investigated.
Untreated sheep erythrocytes were found to adhere toB. leachii haemocytes in vitro. Adherence appeared to be mediated by the HA-2 agglutinin, as evidenced by the inhibition of adhesion by lactose (which is a specific inhibitor of the HA-2 agglutinin) and by an anti-HA-2 IgG preparation. Immunofluorescence studies indicated that HA-2 molecules secreted by the haemocytes bound to unsensitised erythrocytes, causing them to adhere to haemocytes. No HA-2 agglutinin could be detected on the surface of the haemocytes in the absence of erythrocytes but receptors for the agglutinin were detected. The results suggest that the HA-2 agglutinin can function as a recognition molecule for sheep erythrocytes and other particles bearing the appropriate carbohydrate moieties on their surfaces. At least one of two other lectins purified from haemolymph (HA-1 and LBP-3) was detected by immunofluorescence on the surface of haemocytes. The function(2) of these latter molecules, neither of which binds to sheep erythrocytes, is not known.
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Abbreviations
- BSS :
-
Botrylloides salt solution
- HA-1 :
-
haemagglutinin one
- HA-2 :
-
haemagglutinin two
- IgG :
-
immunoglobulin G
- LBP-3 :
-
lactose binding protein three
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Coombe, D.R., Ey, P.L. & Jenkin, C.R. Particle recognition by haemocytes from the colonial ascidianBotrylloides leachii: Evidence that theB. leachii HA-2 agglutinin is opsonic. J Comp Physiol B 154, 509–521 (1984). https://doi.org/10.1007/BF02515156
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DOI: https://doi.org/10.1007/BF02515156