Nf1-/- Schwann Cell-Conditioned Medium Modulates Mast Cell Degranulation by c-Kit-Mediated Hyperactivation of Phosphatidylinositol 3-Kinase

Neurofibromatosis type 1 (NF1) is a common genetic disorder and is characterized by both malignant and nonmalignant neurofibromas which are composed of Schwann cells degranulating mast cells fibroblasts and extracellular matrix We and others have previously shown that hyperactivation of the c Kit pathway in an Nf1 haploinsufficient microenvironment is required for both tumor formation and progression Mast cells play a key role in both tumorigenesis and neoangiogenesis via the production of matrix metalloprotemases heparin and a range of different growth factors In the present study we show that tumorigenic Schwann cells derived from Nf1(-/-) embryos promote increased degranulation of Nf1(+/-) mast cells compared with wild type mast cells via the secretion of the Kit ligand Furthermore we used genetic intercrosses as well as pharmacological agents to link the hyperactivation of the p21(Ra) phosphatidylinositol 3 kinase (PI3K) pathway to the in creased degranulation of Nf1(+/-) mast cells both in vitro and in vivo These studies identify the p21(Ra) PI3K pathway as a major regulator of the gain in Nf1(+/-) mast cell degranulation in neurofibromas Collectively these studies identify both c Kit and PI3K as molecular targets that modulate mast cell functions in cases of NF1 (Am J Pathol 2010 177 3125-3132 DOI 10 2353/ajpath 2010 100369)