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Jiri Kalabis, Kenji Oyama, Takaomi Okawa, Hiroshi Nakagawa, Carmen Z. Michaylira, Douglas B. Stairs, Jose-Luiz Figueiredo, Umar Mahmood, J. Alan Diehl, Meenhard Herlyn, Anil K. Rustgi
Published in Volume 118, Issue 12
J Clin Invest. 2008; 118(12):3860–3869 doi:10.1172/JCI35012
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Figure 5
SP cells are able to differentiate in organotypic culture, giving rise to proliferative basal CK14+CK13CK4 and differentiated suprabasal CK14CK13+CK4+ cells.

(AC) Unsorted freshly isolated WT (GFP) cells did not form an epithelium layer (similar to data shown in Figure 4) with immunohistochemical staining for (A) CK14, (B) CK4, and (C) CK13. (DF) Sorted 103 NSP cells from GFP+ mice mixed with 3 × 104 unsorted GFP cells did not form an epithelium (similar to data shown in Figure 4) with immunohistochemical staining for (D) CK14, (E) CK4, and (F) CK13. (GI) SP cells (103) from GFP+ mice mixed with 3 × 104 unsorted GFP cells formed a complete epithelium with luminal keratinization (similar to data shown in Figure 4) with well-defined proliferative basal and differentiated suprabasal cells. Immunohistochemical staining for (G) CK14, (H) CK4, and (I) CK13. Dashed lines indicate the basement membrane. Original magnification, ×400. Scale bar: 25 μm.