Cloning, expression and characterization of CCL21 and CCL25 chemokines in zebrafish
- Authors
- Lu, I.N., Chiang, B.L., Lou, K.L, Huang, P.T., Yao, C.C., Wang, J.S., Lin, L.D., Jeng, J.H., and Chang, B.E.
- ID
- ZDB-PUB-120807-5
- Date
- 2012
- Source
- Developmental and comparative immunology 38(2): 203-214 (Journal)
- Registered Authors
- Chang, Bei-En
- Keywords
- chemokine, CCL21, CCL25, In situ, zebrafish
- MeSH Terms
-
- Amino Acid Sequence
- Animals
- Chemokine CCL21/chemistry
- Chemokine CCL21/genetics*
- Chemokine CCL21/immunology
- Chemokine CCL21/metabolism
- Chemokines, CC/chemistry
- Chemokines, CC/genetics*
- Chemokines, CC/immunology
- Chemokines, CC/metabolism
- Cloning, Molecular
- Embryo, Nonmammalian/metabolism
- Models, Molecular
- Molecular Sequence Data
- Oocytes/metabolism
- Phylogeny
- Sequence Alignment
- Thymus Gland/embryology
- Thymus Gland/metabolism
- Transcriptome*
- Zebrafish/embryology
- Zebrafish/genetics*
- Zebrafish/immunology
- Zebrafish/metabolism
- Zebrafish Proteins/chemistry
- Zebrafish Proteins/genetics*
- Zebrafish Proteins/immunology
- Zebrafish Proteins/metabolism
- PubMed
- 22842207 Full text @ Dev. Comp. Immunol.
Chemokines are a large group of proteins implicated in migration, activation, and differentiation of leukocytes. They are well-surveyed in mammals, but less is known in lower vertebrates about their spatiotemporal expressions and functions. From an evolutionary point of view, comparative analyses may provide some fundamental insights into these molecules. In mammals, CCL21 and CCL25 are crucial for thymocyte homing. Herein, we identified and cloned the zebrafish orthologues of CCL21 and CCL25, and analyzed their expression in embryos and adult fish by in situ hybridization. We found that CCL21 was expressed in the craniofacial region, pharynx, and blood vessels in embryos. In adult fish, CCL21 transcripts were located in the kidney, spinal cord, and blood cells. In contrast, expression of CCL25 was only detected in the thymus primordia in embryos. In adult fish, transcripts of CCL25 were maintained in the thymus, and they were also found in the brain and oocytes. Furthermore, we performed an antisense oligonucleotide experiment to evaluate the biological function of CCL25. Results showed that the recruitment of thymocytes was impeded by morpholino-mediated knockdown of CCL25, suggesting that CCL25 is essential for colonization of T-cells in the thymus in early development. Together, our results demonstrate the basic profiles of two CCL chemokines in zebrafish. The tissue-specific expression patterns may pave the way for further genetic dissection in this model organism.