KRISHI
ICAR RESEARCH DATA REPOSITORY FOR KNOWLEDGE MANAGEMENT
(An Institutional Publication and Data Inventory Repository)
"Not Available": Please do not remove the default option "Not Available" for the fields where metadata information is not available
"1001-01-01": Date not available or not applicable for filling metadata infromation
"1001-01-01": Date not available or not applicable for filling metadata infromation
Please use this identifier to cite or link to this item:
http://krishi.icar.gov.in/jspui/handle/123456789/77163
Title: | Expression of biologically active bovine interleukin 7 and evaluating the activity in vitro |
Other Titles: | Not Available |
Authors: | J. Lijo N. Vijay H. J. Dechamma G. R. Reddy |
ICAR Data Use Licennce: | http://krishi.icar.gov.in/PDF/ICAR_Data_Use_Licence.pdf |
Author's Affiliated institute: | ICAR- Indian veterinary research institute |
Published/ Complete Date: | 2016-02-13 |
Project Code: | Not Available |
Keywords: | B-cell lymphoma 2 nuclear factor for activated T-cells c1 recombinant bovine interleukin 7 signal transducer and activator 3 |
Publisher: | PubMed Central |
Citation: | Lijo J, Vijay N, Dechamma HJ, Reddy GR. Expression of biologically active bovine interleukin 7 and evaluating the activity in vitro. Vet World. 2016 Feb;9(2):160-5. doi: 10.14202/vetworld.2016.160-165. Epub 2016 Feb 13. PMID: 27051202; PMCID: PMC4819366. |
Series/Report no.: | Not Available; |
Abstract/Description: | Aim: Interleukin 7 (IL-7) is a ϒc family cytokine involved in the homeostatic proliferation and maintenance of immune cells. In the present study, we report the expression of bovine IL-7 (bIL-7) in Escherichia coli and evaluated for its biological activity. Materials and Methods: The sequence coding for bIL-7 (mature protein) was amplified from primary bovine kidney cell culture and cloned into pET28-a vector and expressed in E. coli (BL 21 DE3). The expressed protein was purified by nickel-nitrilotriacetatechromatography, and the reactivity of the protein was confirmed by western blotting using monoclonal antibodies raised against human IL-7. The biological activity of expressed bIL-7 was evaluated by analyzing its effect on the expression of anuclear factor for activated T-cells c1 (NFATc1), B-cell lymphoma 2 (Bcl2), suppressor of cytokine signaling 3 (SOCS3) molecules in bovine peripheral blood mononuclear cells (PBMCs) by quantitative polymerase chain reaction. Ability of the expressed protein was also analyzed by its effect on phosphorylating signal transducer and activator 3 (STAT3) molecule by immunostaining in human embryonic kidney cells 293 (HEK293) cells. Results: The bIL-7 was able to induce the expression of Bcl2 and NFATc1expression in bovine PBMCs by 7 and 5-folds, respectively, whereas a 2-fold decrease was observed in the case of SOCS3 expression. Immunostaining studies in HEK293 cells using antihuman phospho-STAT3 showed activation and nuclear translocation of STAT3 molecule on bIL-7 treatment. Conclusion: bIL-7 gene was successfully amplified, cloned, and expressed in a prokaryotic expression system. The biological activity study showed that the E. coli expressed bIL-7 protein is biologically active. Considering the role of IL-7 in T-cell homeostasis and memory cell generation, this molecule can be used for enhancing the vaccine response and that has to be proved by further experiments. Keywords: B-cell lymphoma 2, nuclear factor for activated T-cells c1, recombinant bovine interleukin 7, signal transducer and activator 3 |
Description: | Not Available |
ISSN: | 2231-0916 |
Type(s) of content: | Research Paper |
Sponsors: | Not Available |
Language: | English |
Name of Journal: | Veterinary World |
Journal Type: | Included as NAAS JOURNAL |
NAAS Rating: | 5.71 |
Impact Factor: | 0.265 |
Volume No.: | 9 |
Page Number: | 160-165 |
Name of the Division/Regional Station: | IVRI, Regional station Bangalore |
Source, DOI or any other URL: | doi: 10.14202/vetworld.2016.160-165 |
URI: | http://krishi.icar.gov.in/jspui/handle/123456789/77163 |
Appears in Collections: | AS-IVRI-Publication |
Files in This Item:
There are no files associated with this item.
Items in KRISHI are protected by copyright, with all rights reserved, unless otherwise indicated.