Neurofibromas from NF1^flox/−;Krox20-cre mice contain multiple cell types. (A) Higher magnification of a neurofibroma demonstrates myelinated axons (N) separated by dissociated Schwann cells (arrows) and collagen bundles (arrowhead). (B) In addition to dissociated Schwann cells, the neurofibroma also contains differentiated Schwann cell processes surrounding individual unmyelinated axons (arrows), suggesting a continuum of dysplastic to overly neoplastic transformation. (C) Electron microscopy analysis demonstrates the presence of perineurial-like cells surrounding axons in a concentric fashion, reminiscent of the multilamellar arrays of perineurial cells seen in human perineuriomas (14). (D) In contrast to Schwann cells elsewhere in the tumor, these perineurial-like cells lack a continuous basal lamina (arrows). Sections from a neurofibroma were stained with H&E (E) and Leder staining, an enzymatic stain for Naphthol AS-D (3-hydroxy-2-naphoic acid-O-toluidine) choloroacetate esterase (F), displaying numerous mast cells (arrowheads) infiltrating the tumors. Scale bar, (A) to (D), 2 μm; (E) and (F), 100 μm.

Histological and molecular analysis of neurofibromas from NF1 ^flox/−;Krox20-cre mice. Sections from a neurofibroma (arrow) associated with cranial nerves were stained with hematoxylin and eosin (H&E) (A and B) and S100 antibody (C). Sections from two neurofibromas (arrows) originating from dorsal root ganglia (DRG) were stained with H&E (D and E) and S100 (F). SC, spinal cord. (G) An example of three macroscopic neurofibromas from spinal roots (right, arrows), as compared to control spinal roots (left, arrowheads). (H) Genomic DNAs isolated from three neurofibromas in (G) (T1 to T3) were subjected to polymerase chain reaction analysis, as described in (11). Cre, genomic DNAs from a NF1^flox/flox Schwann cell culture infected with Cre-expressing adenovirus. Of note, only the recombined allele (Rcre) remains in this culture. LacZ, genomic DNAs from similar Schwann cell culture infected with LacZ-expressing adenovirus. Scale bar, (A) to (F), 25 μm.

Phenotypic comparison of NF1^flox/−;Krox20-cre (CKO^×1+/−) and NF1^flox/flox;Krox20-cre (CKO^×1/×1) mice. (A) Quantification of neurofibromas associated with cranial nerves (CN) and spinal nerves (SN) from 12-month-old (n = 6) and 15-month-old (n = 1) CKO^×1/− mutant mice and of hyperplastic lesions from similar areas of 12-month-old (n = 2) and 15-month-old (n = 1) CKO^×1/×1 mice. Data are means ±SEM, n = 2 to 6, P < 0.01. (B) Neurofibromas (marked by dotted lines) that develop in the CKO^×1/− mice are significantly larger than hyperplastic lesions from CKO^×1/×1 mice. HB, hindbrain. (C) A substantial infiltration of mast cells (arrowheads), identified by Leder staining, found in 6-month-old CKO^×1/− pre-neoplastic cranial and spinal nerves, whereas few mast cells are present in the hyperplastic nerves of 15-month-old CKO^×1/×1 mice. Scale bar, (B), 50 μm; (C), 100 μm.