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. 2007 Nov;171(5):1608–1618. doi: 10.2353/ajpath.2007.060661

Figure 2.

Figure 2

Representative images of cultured CAFs (A) and LFs (B) stained for vimentin, α-SMA, Thy-1, ICAM-1, cytokeratin (CK)-7, laminin, CK-19, and neural cell adhesion molecule (NCAM), indicating that the myofibroblastic phenotype of CAFs and LFs was stable in vitro (original magnification, ×400; positive staining, red).