T-kininogen: A biomarker of aging in fisher 344 rats with possible implications for the immune response
Author
dc.contributor.author
Acuña Castillo, Claudio
Author
dc.contributor.author
Leiva-Salcedo, Elias
Author
dc.contributor.author
Gómez, Christian R.
Author
dc.contributor.author
Pérez, Viviana
Author
dc.contributor.author
Li, Min
Author
dc.contributor.author
Torres, Claudio
Author
dc.contributor.author
Walter, Robin Ann
Author
dc.contributor.author
Murasko, Donna M.
Author
dc.contributor.author
Sierra, Felipe
Admission date
dc.date.accessioned
2019-03-11T12:51:16Z
Available date
dc.date.available
2019-03-11T12:51:16Z
Publication date
dc.date.issued
2006
Cita de ítem
dc.identifier.citation
Journals of Gerontology - Series A Biological Sciences and Medical Sciences, Volumen 61, Issue 7, 2018, Pages 641-649
Identifier
dc.identifier.issn
10795006
Identifier
dc.identifier.other
10.1093/gerona/61.7.641
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/164176
Abstract
dc.description.abstract
T-kininogen (T-KG) is a reliable biomarker of aging in male Sprague-Dawley rats. Here we confirm, in a longitudinal study, a similar behavior in Fisher 344 rats of both sexes. In males, the increase in serum levels of T-KG follows an exponential curve, whereas in females the increase is best fitted by a linear curve. In both genders, dietary restriction delays the increase in T-KG. We have previously shown that T-KG inhibits T lymphocyte proliferation. Here we show that serum T-KG levels correlate negatively with the ability of splenocytes (most likely B cells) to proliferate in response to lipopolysaccharide. A similar correlation was not observed with other markers of inflammation, including α1-acid glycoprotein (AGP), haptoglobin, or interleukin-10. We conclude that the increase in serum T-KG represents a useful biomarker of aging in Fisher 344, and it correlates with decreased lymphocyte proliferation with age, although a cause-effect relationship has not been established. Copyrigh