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Hemolectin expression reveals functional heterogeneity in honey bee (Apis mellifera) hemocytes.
- Source :
-
Developmental and comparative immunology [Dev Comp Immunol] 2017 Nov; Vol. 76, pp. 403-411. Date of Electronic Publication: 2017 Jul 13. - Publication Year :
- 2017
-
Abstract
- The identification of molecular markers considerably facilitated the classification and functional analysis of blood cell types. Apis mellifera hemocytes have been classified by morphological criteria and lectin binding properties; however, the use of molecular markers has been minimal. Here we describe a monoclonal antibody to a non-phagocytic subpopulation of A. mellifera hemocytes and to a constituent of the hemolymph clot. We demonstrate that the antibody identifies the A. mellifera hemolectin, a protein carrying human von Willebrand factor homology domains, characteristic of proteins involved in blood coagulation and platelet aggregation in mammals. Hemolectin expressing A. mellifera hemocytes contain the protein as cytoplasmic granules and contribute to the formation of a protein matrix, building up around foreign particles. Consequently, hemolectin as a marker molecule reveals a clear functional heterogeneity of hemocytes, allowing for the analytical separation of hemocyte classes, and could promote the molecular identification of hemocyte lineages in A. mellifera.<br /> (Copyright © 2017 Elsevier Ltd. All rights reserved.)
- Subjects :
- Animals
Antibodies, Monoclonal isolation & purification
Biodiversity
Cell Separation
Lectins genetics
Lectins immunology
Mammals
Phagocytosis
Platelet Aggregation genetics
Sequence Homology, Amino Acid
Transcriptome
von Willebrand Factor genetics
Bees immunology
Hemocytes physiology
Hemolymph metabolism
Lectins metabolism
Thrombosis metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1879-0089
- Volume :
- 76
- Database :
- MEDLINE
- Journal :
- Developmental and comparative immunology
- Publication Type :
- Academic Journal
- Accession number :
- 28713010
- Full Text :
- https://doi.org/10.1016/j.dci.2017.07.013