The SH2-domain-containing inositol 5-phosphatase (SHIP) limits neutrophil motility and wound recruitment in zebrafish
- Authors
- Lam, P.Y., Yoo, S.K., Green, J.M., and Huttenlocher, A.
- ID
- ZDB-PUB-120905-23
- Date
- 2012
- Source
- Journal of Cell Science 125(21): 4973-4978 (Journal)
- Registered Authors
- Huttenlocher, Anna, Lam, Pui Ying
- Keywords
- none
- MeSH Terms
-
- Animals
- Cell Movement
- Embryo, Nonmammalian/cytology
- Embryo, Nonmammalian/enzymology
- Embryo, Nonmammalian/immunology
- Gene Expression
- Neutrophils/enzymology*
- Neutrophils/immunology
- Neutrophils/physiology
- Phosphatidylinositol 3-Kinases/metabolism
- Phosphatidylinositol Phosphates/metabolism
- Phosphoric Monoester Hydrolases/genetics
- Phosphoric Monoester Hydrolases/metabolism*
- Protein Transport
- Second Messenger Systems
- Tail
- Time-Lapse Imaging
- Wound Healing*
- Zebrafish
- Zebrafish Proteins/genetics
- Zebrafish Proteins/metabolism*
- PubMed
- 22946052 Full text @ J. Cell Sci.
Neutrophil recruitment to sites of injury or infection is essential for host defense, but it needs to be tightly regulated to prevent tissue damage. Phosphoinositide 3-kinase (PI3K), that generates the phosphoinositide PI(3,4,5)P3, is necessary for neutrophil motility in vivo, however, the role of SH2-domain–containing 5-inositol phosphatase (SHIP) enzymes, that hydrolyzes PI(3,4,5)P3 to PI(3,4)P2, is not well understood. Here we show that SHIP phosphatases limit neutrophil motility in live zebrafish. Using real-time imaging of bioprobes specific for PI(3,4,5)P3 and PI(3,4)P2 in neutrophils, we found that PI(3,4,5)P3 and PI(3,4)P2 accumulate at the leading edge while PI(3,4)P2 also localizes to the trailing edge of migrating neutrophils in vivo. Depletion of SHIP phosphatases using morpholinos led to increased neutrophil 3D motility and neutrophil infiltration into wounds. The increase in neutrophil wound recruitment in SHIP morphants was rescued by treatment with low dose PI3Kγ inhibitor, suggesting that SHIP limits neutrophil motility by modulating PI3K signaling. Moreover, overexpression of the SHIP phosphatase domain in neutrophils impaired neutrophil 3D migration. Taken together, our findings suggest that SHIP phosphatases control neutrophil inflammation by limiting neutrophil motility in vivo.