Point mutations of single amino acids abolish ability of alpha(3) NC1 domain to elicit experimental autoimmune glomerulonephritis in rats
(2003) In Journal of Biological Chemistry 278(47). p.46516-46522- Abstract
- We previously showed concordance between Goodpasture syndrome antibody binding and production of experimental glomerulonephritis using human chimeric proteins. We now examine a more limited aminoterminal region of alpha(3)( IV) non- collagenous domain ( NC1) and the impact of single amino acid ( AA) mutations of this region on glomerulonephritis induction. Rats were immunized with collagenase- solubilized glomerular basement membrane ( csGBM), D3, an alpha(1)( IV) NC1 chimeric protein with 69 AA of alpha(3)( IV) NC1 ( binds Goodpasture sera), D4, the D3 construct shortened by 4 AA ( nonbinding), P9, P10, single AA mutants ( non- binding), and S2, alpha(1)( IV) NC1 with 9 AA of alpha(3)( IV) NC1 ( binding). All rats immunized with csGBM and... (More)
- We previously showed concordance between Goodpasture syndrome antibody binding and production of experimental glomerulonephritis using human chimeric proteins. We now examine a more limited aminoterminal region of alpha(3)( IV) non- collagenous domain ( NC1) and the impact of single amino acid ( AA) mutations of this region on glomerulonephritis induction. Rats were immunized with collagenase- solubilized glomerular basement membrane ( csGBM), D3, an alpha(1)( IV) NC1 chimeric protein with 69 AA of alpha(3)( IV) NC1 ( binds Goodpasture sera), D4, the D3 construct shortened by 4 AA ( nonbinding), P9, P10, single AA mutants ( non- binding), and S2, alpha(1)( IV) NC1 with 9 AA of alpha(3)( IV) NC1 ( binding). All rats immunized with csGBM and S2 and 50% of D3 rats developed glomerulonephritis. csGBM rats had intense GBM- bound IgG deposits, but S2 and D3 rats had minimal deposits. None of the D4, P9, or P10 rats developed glomerulonephritis. Lymphocytes from nephritic rats proliferated with csGBM, S2, and D3, but not with D4, P9, or P10. Discrete segments of alpha(3)( IV) NC1 within the alpha(1)( IV) NC1 backbone can induce glomerulonephritis. Single AA mutations within that epitope render the antigen unresponsive to Goodpasture sera and incapable of inducing glomerulonephritis. These studies support the concordance of glomerulonephritis inductivity and Goodpasture serum binding. Further, they define a critical limited AA sequence within alpha(3)( IV) NC1 of nine or fewer AA, which confers nephritogenicity to the non-nephritogenic alpha(1)( IV) NC1 without in vivo antibody binding. This region may be a T- cell epitope responsible for induction of glomerulonephritis in this model in rats and Goodpasture syndrome in man. (Less)
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https://lup.lub.lu.se/record/295041
- author
- Hellmark, Thomas LU ; Chen, LL ; Ohlsson, Sophie LU ; Wieslander, R and Bolton, WK
- organization
- publishing date
- 2003
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Journal of Biological Chemistry
- volume
- 278
- issue
- 47
- pages
- 46516 - 46522
- publisher
- American Society for Biochemistry and Molecular Biology
- external identifiers
-
- wos:000186569400036
- scopus:0344875580
- pmid:12970356
- ISSN
- 1083-351X
- DOI
- 10.1074/jbc.M211951200
- language
- English
- LU publication?
- yes
- id
- 8a95bc68-7975-48a3-96c8-582d670d72b7 (old id 295041)
- date added to LUP
- 2016-04-01 12:19:38
- date last changed
- 2022-01-27 02:07:15
@article{8a95bc68-7975-48a3-96c8-582d670d72b7, abstract = {{We previously showed concordance between Goodpasture syndrome antibody binding and production of experimental glomerulonephritis using human chimeric proteins. We now examine a more limited aminoterminal region of alpha(3)( IV) non- collagenous domain ( NC1) and the impact of single amino acid ( AA) mutations of this region on glomerulonephritis induction. Rats were immunized with collagenase- solubilized glomerular basement membrane ( csGBM), D3, an alpha(1)( IV) NC1 chimeric protein with 69 AA of alpha(3)( IV) NC1 ( binds Goodpasture sera), D4, the D3 construct shortened by 4 AA ( nonbinding), P9, P10, single AA mutants ( non- binding), and S2, alpha(1)( IV) NC1 with 9 AA of alpha(3)( IV) NC1 ( binding). All rats immunized with csGBM and S2 and 50% of D3 rats developed glomerulonephritis. csGBM rats had intense GBM- bound IgG deposits, but S2 and D3 rats had minimal deposits. None of the D4, P9, or P10 rats developed glomerulonephritis. Lymphocytes from nephritic rats proliferated with csGBM, S2, and D3, but not with D4, P9, or P10. Discrete segments of alpha(3)( IV) NC1 within the alpha(1)( IV) NC1 backbone can induce glomerulonephritis. Single AA mutations within that epitope render the antigen unresponsive to Goodpasture sera and incapable of inducing glomerulonephritis. These studies support the concordance of glomerulonephritis inductivity and Goodpasture serum binding. Further, they define a critical limited AA sequence within alpha(3)( IV) NC1 of nine or fewer AA, which confers nephritogenicity to the non-nephritogenic alpha(1)( IV) NC1 without in vivo antibody binding. This region may be a T- cell epitope responsible for induction of glomerulonephritis in this model in rats and Goodpasture syndrome in man.}}, author = {{Hellmark, Thomas and Chen, LL and Ohlsson, Sophie and Wieslander, R and Bolton, WK}}, issn = {{1083-351X}}, language = {{eng}}, number = {{47}}, pages = {{46516--46522}}, publisher = {{American Society for Biochemistry and Molecular Biology}}, series = {{Journal of Biological Chemistry}}, title = {{Point mutations of single amino acids abolish ability of alpha(3) NC1 domain to elicit experimental autoimmune glomerulonephritis in rats}}, url = {{http://dx.doi.org/10.1074/jbc.M211951200}}, doi = {{10.1074/jbc.M211951200}}, volume = {{278}}, year = {{2003}}, }