309 Tumor Necrosis Factor-Inducible Gene 6 Protein: A Novel Neuroprotective Factor Against Inflammatory Developmental Brain Injury. (October 2012)
- Record Type:
- Journal Article
- Title:
- 309 Tumor Necrosis Factor-Inducible Gene 6 Protein: A Novel Neuroprotective Factor Against Inflammatory Developmental Brain Injury. (October 2012)
- Main Title:
- 309 Tumor Necrosis Factor-Inducible Gene 6 Protein: A Novel Neuroprotective Factor Against Inflammatory Developmental Brain Injury
- Authors:
- Bertling, F
Prager, S
Hermann, R
Bendix, I
Wisniewski, HG
FelderhoffMüser, U
Keller, M - Abstract:
- Abstract : Background and Aims: An important factor of developmental brain injury is inflammation. It has been shown that tumor necrosis factor-inducible gene 6 protein (TSG-6) has anti-inflammatory effects in several inflammatory conditions. Nothing is known so far about the role of TSG-6 in the developing brain, its impact on inflammation and its therapeutic potential. Methods: PCR, Western Blotting and Immunohistochemistry was performed according to standard protocols. Brain hemispheres of untreated Wistar rats (p1-p15) were evaluated under developmental aspects of TSG-6. LPS-treated rats (0.25mg/kg LPS i.p. on p3) were evaluated under pathological aspects of TSG-6. To evaluate whether exogenous rhTSG-6 reduces inflammatory-induced brain injury, newborn Wistar rats, exposed to LPS at p3, were treated with rhTSG-6 i.p. (four repetitive doses of 2.25mg/kg every 12h, first dose three hours before LPS-injection). Results: Investigations of TSG-6's developmental brain expression showed a linear increase from p1 to p15 on gene level. Additionally, different expression was detected in Cortex, Thalamus and Striatum on gene level at p6. Expression of TSG-6 after LPS treatment (0–24h) was significantly increased on gene level and tendentiously on protein level. cCaspase-3, a marker of apoptosis, showed a significant down-regulation of >30% under additional TSG-6 treatment versus sole LPS exposure (n=12–14, p=0, 025). Conclusions: TSG-6 Expression is developmentally regulated andAbstract : Background and Aims: An important factor of developmental brain injury is inflammation. It has been shown that tumor necrosis factor-inducible gene 6 protein (TSG-6) has anti-inflammatory effects in several inflammatory conditions. Nothing is known so far about the role of TSG-6 in the developing brain, its impact on inflammation and its therapeutic potential. Methods: PCR, Western Blotting and Immunohistochemistry was performed according to standard protocols. Brain hemispheres of untreated Wistar rats (p1-p15) were evaluated under developmental aspects of TSG-6. LPS-treated rats (0.25mg/kg LPS i.p. on p3) were evaluated under pathological aspects of TSG-6. To evaluate whether exogenous rhTSG-6 reduces inflammatory-induced brain injury, newborn Wistar rats, exposed to LPS at p3, were treated with rhTSG-6 i.p. (four repetitive doses of 2.25mg/kg every 12h, first dose three hours before LPS-injection). Results: Investigations of TSG-6's developmental brain expression showed a linear increase from p1 to p15 on gene level. Additionally, different expression was detected in Cortex, Thalamus and Striatum on gene level at p6. Expression of TSG-6 after LPS treatment (0–24h) was significantly increased on gene level and tendentiously on protein level. cCaspase-3, a marker of apoptosis, showed a significant down-regulation of >30% under additional TSG-6 treatment versus sole LPS exposure (n=12–14, p=0, 025). Conclusions: TSG-6 Expression is developmentally regulated and increased after LPS exposure. The reduction of activated Caspase-3 demonstrates the neuroprotective potential of exogenous TSG-6 administration in inflammatory-induced developmental brain injury. … (more)
- Is Part Of:
- Archives of disease in childhood. Volume 97(2012)Supplement 2
- Journal:
- Archives of disease in childhood
- Issue:
- Volume 97(2012)Supplement 2
- Issue Display:
- Volume 97, Issue 2 (2012)
- Year:
- 2012
- Volume:
- 97
- Issue:
- 2
- Issue Sort Value:
- 2012-0097-0002-0000
- Page Start:
- A90
- Page End:
- A91
- Publication Date:
- 2012-10
- Subjects:
- Children -- Diseases -- Periodicals
Infants -- Diseases -- Periodicals
618.920005 - Journal URLs:
- http://adc.bmjjournals.com/ ↗
http://www.bmj.com/archive ↗ - DOI:
- 10.1136/archdischild-2012-302724.0309 ↗
- Languages:
- English
- ISSNs:
- 0003-9888
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 18426.xml