Effect of TNF-alpha on CD3-zeta and MHC-I in postnatal rat hippocampus.

Abstract:

:The zeta subunit of the CD3 T-cell receptor complex and the major histocompatibility complex class 1 (MHC-I) are important not only for the immune response to antigens, they also function as signal molecules in the brain, where they play a role in the postnatal maturation process. The expression of these molecules can be regulated by cytokines. In situations associated with increased cytokine production, such as neonatal hypoxia, the hippocampus is particularly susceptible to permanent damage. This has prompted us to examine the MHC-I and CD3-zeta expression in hippocampus from early postnatal, weanling and adolescent rats and to record the effects of TNF-alpha and IL-1beta, cytokines commonly increased in neonatal hypoxia, on MHC-I and CD3-zeta expression in the hippocampus. We show that there is a robust postnatal up-regulation of CD3-zeta and MHC-I protein as well as of MHC-I mRNA and that TNF-alpha down-regulates the expression of CD3-zeta protein and MHC-I mRNA in early postnatal but not in weanling nor in adolescent rats. These results may offer a molecular explanation to the adverse effects of increased circulating levels of cytokines on brain in neonatal hypoxia.

journal_name

Pediatr Res

journal_title

Pediatric research

authors

Sourial-Bassillious N,Eklöf AC,Scott L,Aperia A,Zelenin S

doi

10.1203/01.pdr.0000238246.74817.a0

subject

Has Abstract

pub_date

2006-10-01 00:00:00

pages

377-81

issue

4

eissn

0031-3998

issn

1530-0447

pii

01.pdr.0000238246.74817.a0

journal_volume

60

pub_type

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