Immunohistochemical Demonstration of Hyaluronan and Its Possible Involvement in Axolotl Neural Crest Cell Migration

• Published in: Journal of structural biology 2000-10, Vol.132 (1), p.19-32
• Main Authors: Epperlein, Hans-Henning, Radomski, Norbert, Wonka, Fred, Walther, Paul, Wilsch, Michaela, Müller, Martin, Schwarz, Heinz
• Format: Article
• Language: English
• Subjects: Ambystoma - embryology; Animals; axolotl; Basement Membrane - chemistry; Basement Membrane - ultrastructure; Cell Movement - drug effects; Cell Movement - physiology; cryoimmobilization; Cryopreservation; Extracellular Matrix - chemistry; Extracellular Matrix - ultrastructure; hyaluronan; Hyaluronic Acid - pharmacology; Hyaluronic Acid - physiology; Hyaluronic Acid - ultrastructure; Immunohistochemistry; Microscopy, Electron - methods; neural crest; Neural Crest - chemistry; Neural Crest - cytology; Neural Crest - embryology; Tissue Fixation
• ISSN: 1047-8477; 1095-8657
• DOI: 10.1006/jsbi.2000.4298

Hyaluronan (HA), an extracellular matrix component, is involved mainly in the control of cell proliferation, neural crest and tumor cell migration, and wound repair. We investigated the effect of hyaluronan on neural crest (NC) cell migration and its ultrastructural localization in dark (wild-type) and white mutant embryos of the Mexican axolotl (Ambystoma mexicanum, Amphibia). The axolotl system is an accepted model for studying mechanims of NC cell migration. Using a biotinylated hyaluronan binding protein (HABP), major extracellular matrix (ECM) spaces, including those of NC cell migration, reacted equally positive on cryosections through dark and white embryos. Since neural crest-derived pigment cells migrate only in subepidermal spaces of dark embryos, HA does not seem to influence crest cell migration in vivo. However, when tested on different alternating substrates in vitro, migrating NC cells in dark and white embryos prefer HA to fibronectin. In vivo, such an HA migration stimulating effect might exist as well, but be counteracted to differing degrees in dark and white embryos. The ultrastructural localization of HA was studied by means of transmission electron microscopic immunohistochemistry using HABP and different protocols of standard chemical fixation, cryofixation, embedding, and immunolabeling. The binding reaction of HA to HABP was strong and showed an equal distribution throughout ECM spaces after both standard chemical fixation/freeze substitution and cryofixation. A preference for the somite or subepidermal side was not observed. Following standard fixation/freeze substitution HABP-labeled “honeycomb”-like networks reminiscent of fixation artifacts were more prominent than labeled fibrillar or irregular net-like structures. The latter predominated in adequately frozen specimens following high-pressure freezing/freeze substitution. For this reason fibrillar or irregular net-like structures very likely represent hyaluronan in the complex subepidermal matrix of the axolotl embryo in its native arrangement.