Immunohistochemical localization of calcium-binding proteins (CaBPs) in the epidermis of the earthworm Lumbricus terrestris (Annelida, Oligochaeta)

• Published in: Acta histochemica Vol. 102; no. 2; pp. 159 - 166
• Main Authors: Licata, Aurelio, Mauceri, Angela, Ricca, Maria B., Lo Cascio, Patrizia, Martella, Silvestro, Amato, Aldo
• Format: Journal Article
• Language: English
• Published: Germany Elsevier GmbH 2000
• Subjects: Animals; annelida; Calbindins; calcium binding proteins; Calcium-Binding Proteins - immunology; Calcium-Binding Proteins - metabolism; Calmodulin - metabolism; Cytoskeleton - metabolism; epidermis; Fluorescent Antibody Technique, Indirect; Immunoenzyme Techniques; Immunohistochemistry; Oligochaeta - metabolism; Parvalbumins - metabolism; S100 Calcium Binding Protein G - metabolism; S100 Proteins - metabolism; Skin - cytology; Skin - metabolism; Water-Electrolyte Balance - physiology; annelida; immunohistochemistry; calcium binding proteins; epidermis
• ISSN: 0065-1281; 1618-0372
• DOI: 10.1078/S0065-1281(04)70025-2

The present immunohistochemical study provides the first evidence of the presence of calcium-binding proteins (CaBPs) in the epidermis of the earthworm Lumbricus terrestris (Annelida, Oligochaeta) a lower invertebrate. The entire epidermis was labelled for calmodulin which is in agreement with its ubiquitous occurrence. Immunopositivity for calbindin D28K was limited to mucous cells, while that for S-100 protein was present only in neuroendocrine-like small granular cells. Finally, labelling for parvalbumin was specifically present in the subcutaneous nerve plexus. S-100 protein is considered to be a marker of neuroendocrine cells, at least in lower invertebrates such as Annelida. Although calbindin D28K is considered to be a marker of these cells in vertebrates, the same function cannot be attributed in Lumbricus terrestris. However, we can conclude that S-100 protein, as a regulatory protein, is phylogenetically older than calbindin D28K. We assume that the latter has an autoregulatory function in secretory processes. In agreement with previous data, we suggest that small granular cells exert a paracrine action in osmoregulatory and secretory processes.