Characterization of beta-keratins and associated proteins in adult and regenerating epidermis of lizards

• Published in: Tissue & cell 2004-10, Vol.36 (5), p.333-349
• Main Authors: Alibardi, L., Spisni, E., Frassanito, A.G., Toni, M.
• Format: Article
• Language: English
• Subjects: Animals; Autoradiography; Beta-keratin; Collagen - biosynthesis; Collagen - isolation & purification; Cytoskeleton - metabolism; Cytoskeleton - ultrastructure; Dermis - metabolism; Dermis - ultrastructure; Epidermis; Epidermis - metabolism; Epidermis - ultrastructure; Female; Histidine - metabolism; Immunoblotting; Immunocytochemistry; Immunohistochemistry; Keratinocytes - metabolism; Keratinocytes - ultrastructure; Keratins - biosynthesis; Keratins - isolation & purification; Keratins - metabolism; Keratins - ultrastructure; Lizard; Lizards - anatomy & histology; Lizards - metabolism; Male; Microscopy, Electron, Transmission; Molecular Weight; Proline - metabolism; Proline-histidine autoradiography; Regeneration - physiology; Ribosomes - metabolism
• ISSN: 0040-8166; 1532-3072
• DOI: 10.1016/j.tice.2004.06.001

Reptilian epidermis contains two types of keratin, soft (alpha) and hard (beta). The biosynthesis and molecular weight of beta-keratin during differentiation of lizard epidermis have been studied by autoradiography, immunocytochemistry and immunoblotting. Tritiated proline is mainly incorporated into differentiating and maturing beta-keratin cells with a pattern similar to that observed after immunostaining with a chicken beta-keratin antibody. While the antibody labels a mature form of beta-keratin incorporated in large filaments, the autoradiographic analysis shows that beta-keratin is produced within the first 30 min in ribosomes, and is later packed into large filaments. Also the dermis incorporates high amount of proline for the synthesis of collagen. The skin was separated into epidermis and dermis, which were analyzed separately by protein extraction and electrophoresis. In the epidermal extract proline-labeled proteic bands at 10, 15, 18–20, 42–45, 52–56, 85–90 and 120 kDa appear at 1, 3 and 5 h post-injection. The comparison with the dermal extract shows only the 85–90 and 120 kDa bands, which correspond to collagen. Probably the glycine-rich sequences of collagen present also in beta-keratins are weakly recognized by the beta-1 antibody. Immunoblotting with the beta-keratin antibody identifies proteic bands according to the isolation method. After-saline or urea–thiol extraction bands at 10–15, 18–20, 40, 55 and 62 kDa appear. After extraction and carboxymethylation, weak bands at 10–15, 18–20 and 30–32 kDa are present in some preparations, while in others also bands at 55 and 62 kDa are present. It appears that the lowermost bands at 10–20 kDa are simple beta-keratins, while those at 42–56 kDa are complex or polymeric forms of beta-keratins. The smallest beta-keratins (10–20 kDa) may be early synthesized proteins that are polymerized into larger beta-keratins which are then packed to form larger filaments. Some proline-labeled bands differ from those produced after injection of tritiated histidine. The latter treatment does not show 10–20 kDa labeled proteins, but tends to show bands at 27, 30–33, 40–42 and 50–62 kDa. Histidine-labeled proteins mainly localize in keratohyalin-like granules and dark keratin bundles of clear-oberhautchen layers of lizard epidermis, and their composition is probably different from that of beta-keratin.