Materials and Reagents
- Neural buffered formalin (Sigma-Aldrich, catalog number: HT5014 )
- Alcian blue 8GX (Sigma-Aldrich, catalog number: A5268 )
- Trypsin (Sigma-Aldrich, catalog number: T1426 )
- Saturated sodium borate (Sigma-Aldrich, catalog number: S9640 )
- Alizarin red (Sigma-Aldrich, catalog number: A3882 )
- Thymol (EM Life Science, catalog number: TX0615-1 )
- Ethanol
- Glacial acetic acid
- Potassium hydroxide
- Glycerol
- KOH
- Trypsin solution (see Recipes)
Equipment
- Conical tube
Procedure
- Adults:
- Fix mouse skeleton in 10% neutral buffered formalin for at least 24 h.
- Rinse the sample in ddH2O O/N (1 h for embryos) with gentle shaking, and post-fix it in 70% ethanol.
Note: At this point, samples can be stored in 70% ethanol for a long period.
- Remove skins and internal organs carefully from the sample.
Note: Remove all skins, even those on the small toes.
- Stain the sample with 0.02% Alcian blue 8GX (prepared in ethanol/ glacial acetic acid, 7:3) for 1 to 2 days.
Note: Cartilage tissues will be stained blue.
- Wash the sample with plain ethanol/ glacial acetic acid (7:3) for 1 h.
- Soak the sample in 100% ethanol O/N, and then in ddH2O for 1 to 2 days.
- Treat the sample with 1.0% trypsin (prepared in water solution containing 30% saturated sodium borate) O/N.
- Should limp and blue cartilage be readily observed at this point, proceed to stain the sample with Alizarin red (prepared in 0.5% KOH) O/N.
Note: Add enough (no specific amount) saturated Alizarin red until the solution appears dark purple. Mineralized bones will be stained red.
- Treat the sample with a gradient series of 0.5% KOH/ glycerol (i.e., 2:1, 1:1, 1:2 and 100% glycerol, 2 days for each step), and store it in glycerol with a crystal of thymol.
- Embryos:
- A similar protocol can be used to stain embryos. To do this, fix embryos in 90% ethanol for at least 1 week.
- Treat the sample with 0.01% Alcian blue 8GX for 3 days, and then perform rehydration through a gradient series of ethanol (70% ethanol, 2 to 3 h, twice; 40% ethanol, 2 to 3 h; 15% ethanol, 2 to 3 h; ddH2O, until the sample sinks to the bottom of a conical tube). Treat the sample further with fresh 1% KOH for 1 to 2 days until it becomes clear.
- Treat the sample with 0.001% Alizarin red for 2 to 3 days until the bone becomes purple.
- Rinse the sample ~ 3 times in 1% KOH, several hours each time.
- Treat the sample through a gradient series of glycerol-KOH (20% glycerol/ 1% KOH, 24 h; 50% glycerol/ 1% KOH, 24 h; 80% glycerol/ 1% KOH, 24 h; 100% glycerol, 24 h x 2).
Representative data

Figure 1. This figure is adapted from the original (Zhang et al., 2002). Shown here is Alizarin Red (mineralized bone) and Alcian Blue (cartilage) skeletal staining of 18-day-old wild-type A and Perk-/- mutant mice B. The mineralization of the flat bones of the skull (P, parietal; O, occipital; T, temporal) is greatly reduced in the Perk-/- mutant mouse.
Recipes
- Trypsin solution
1.0% trypsin
30% saturated sodium borate
H2O
Acknowledgments
This protocol was adapted from previously described work by Hanken and Wassersug (Hanken and Wassersug, 1981). PZ was supported by a research assistantship in the Cavener lab at the Pennsylvania State University. This work was supported by an NIH R01 grant awarded to DC.
References
- Hanken, J., Wassersug, R. J. (1981). The visible skeleton. Funct Photogr 16(4): 22-26, 44.
- Zhang, P., McGrath, B., Li, S., Frank, A., Zambito, F., Reinert, J., Gannon, M., Ma, K., McNaughton, K. and Cavener, D. R. (2002). The PERK eukaryotic initiation factor 2 alpha kinase is required for the development of the skeletal system, postnatal growth, and the function and viability of the pancreas. Mol Cell Biol 22(11): 3864-3874.
Article Information
Copyright
© 2012 The Authors; exclusive licensee Bio-protocol LLC.
Category
Developmental Biology > Morphogenesis