Contribution of the Innate Immune System to Autoimmune Diabetes: A Role for the CR1/CR2 Complement Receptors

1999 ◽  
Vol 195 (1) ◽  
pp. 75-79 ◽  
Author(s):  
Hooman Noorchashm ◽  
Daniel J. Moore ◽  
Yen K. Lieu ◽  
Negin Noorchashm ◽  
Alexander Schlachterman ◽  
...  
1999 ◽  
Vol 198 (2) ◽  
pp. 143
Author(s):  
Hooman Noorchashm ◽  
Daniel J. Moore ◽  
Yen K. Lieu ◽  
Negin Noorchashm ◽  
Alexander Schlachterman ◽  
...  

2018 ◽  
Author(s):  
Quigly Dragotakes ◽  
Man Shun Fu ◽  
Arturo Casadevall

AbstractCryptococcus neoformansis a pathogenic yeast capable of a unique and intriguing form of cell-to-cell transfer between macrophage cells. The mechanism for cell-to-cell transfer is not understood. Here we imaged macrophages with CellTracker Green CMFDA-labeled cytosol to ascertain whether cytosol was shared between donor and acceptor macrophages. Analysis of several transfer events detected no transfer of cytosol from donor to acceptor macrophages. However, blocking Fc and complement receptors resulted in a major diminution of cell-to-cell transfer events. The timing cell-to-cell transfer (11.17 min) closely approximated the sum of phagocytosis (4.18 min) and exocytosis (6.71 min) times. We propose that macrophage cell-to-cell transfer represents a non-lytic exocytosis event followed by phagocytosis into a macrophage that is in close proximity and name this process Dragotcytosis (Dragot is a Greek surname meaning ‘Sentinel’) as it represents sharing of a microbe between two sentinel cells of the innate immune system.


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