Imune-pineal Axis: injury shifts melatonin production from endocrine to paracrine
Characterization of the immune-pineal axis: the pineal gland as a target for LPS
Induction of melatonin synthesis by glia and neurons in injured central nervous sy...
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Author(s): |
Cláudia Emanuele Carvalho de Sousa
Total Authors: 1
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Document type: | Master's Dissertation |
Press: | São Paulo. |
Institution: | Universidade de São Paulo (USP). Instituto de Biociências (IBIOC/SB) |
Defense date: | 2011-03-28 |
Examining board members: |
Regina Pekelmann Markus;
Thiago Mattar Cunha;
Alexandre Denadai Souza
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Advisor: | Regina Pekelmann Markus |
Abstract | |
TNF acts directly on the pineal gland by inhibiting the biosynthesis of melatonin. Similarly, LPS, a potent activator of the innate immune response has an inhibitory effect on the production of melatonin and its precursor. The suppression of nocturnal melatonin synthesis is admitted to allow the full mounting of the inflammatory response both during the day and night. Data from our laboratory have shown that the NFKB is constitutively expressed in the pineal gland and that the daily rate of translocation can be determinant for the onset of melatonin synthesis. Inhibition of their activation potentiates melatonin synthesis whereas factors that promote its activation classically inhibit this production. In this dissertation we find the molecules involved in recognition and signaling of this cytokine in the pineal. We demonstrated that the pineal is responsive to TNF, the pineal glial cells and secretory cells, the pinealocytes, constitutively express the TNF-R1. TNF promotes nuclear translocation of p50/RelA and p50/p50 NFKB dimers in the pineal glands in culture. We confirmed the activation of this pathway in pinealocytes by analyzing the inhibitory protein IKB. We have seen that the activation of this factor is essential for iNOS expression and NO production induced by TNF in isolated pinealocytes. Furthermore we show that TNF promotes the reduction of the expression of TNF-R1 receptor on the membrane of pinealocytes. In summary, we show here that the pineal is instrumented to respond to TNF and that the pinealocytes are direct targets for its recognition. We confirm the relevance of NFKB in the pineal response in situations of injury extending the concept that the pineal is able to detect molecules in the inflammatory process and respond accordingly. (AU) |