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. Author manuscript; available in PMC: 2014 Apr 7.
Published in final edited form as: Cell Tissue Res. 2014 Jan 30;356(1):137–145. doi: 10.1007/s00441-013-1785-5

Fig. 4.

Fig. 4

The histology, and vascularization of the mouse molar mesenchyme examined by CD31 immunohistochemistry after z-VAD-fmk treatment. E14.0 first lower molars were cultured in vitro in control medium (ac, j) or in the presence of 50 (df, k) or 100 μM (gi, l) z-VAD-fmk for 2 days, then cultured under mouse kidney capsules for 0 (j), 2 (ai), or 4 days (k, l). ac In the control molars, blood vessels appeared in the central part of the dental papilla after 2-day subrenal culture. d–i Blood vessels were only localized in the mandibular portion of the dental mesenchyme and the surrounding tissue in the 50-μM group (df) and in the 100-μM group (gi) after 2-day subrenal culture. j Blood vessels are only detected in the surrounding dental follicle in the molars cultured in vitro in control medium for 2 days. k, lCapillaries are noted not only in the dental follicle but also in the dental papilla after a 2-day culture with the presence of z-VAD-fmk and a following 4-day subrenal culture. a, d, g H&E staining; b, c, e, f, hl CD31 immunostaining. Bars (a, b, d, e, g, h, jl) 100 μm, c, f, i 50 μm