Region-specific difference in apoE4-dependent glial responses to focal brain injury
- 주제(키워드) Apolipoprotein E , focal brain injury , injury repair , glial activation
- 주제(DDC) 570
- 발행기관 아주대학교
- 지도교수 박선아
- 발행년도 2022
- 학위수여년월 2022. 2
- 학위명 석사
- 학과 및 전공 일반대학원 의생명과학과
- 실제URI http://www.dcollection.net/handler/ajou/000000031375
- 본문언어 영어
- 저작권 아주대학교 논문은 저작권에 의해 보호받습니다.
초록/요약
Apolipoprotein E (apoE) involves in various physiological functions including lipid transports, synaptic plasticity and immune modulation. Epidemiological studies suggest that apoE4 isoform increase the risk of post-traumatic sequelae. To understand the involvement of apoE4 on the clinical heterogeneity of posttraumatic neurodegeneration the region-specific effect of apoE4 was studies. Two focal brain injuries were produced separately into motor cortex and hippocampus within a mouse. ApoE4 (4KI) and apoE3 knock-in (3KI), apoE knock-out, and wildtype mice were used for this study. The diminished injury recovery after focal damage was noted in hippocampus of 4KI mice compared to 3KI mice at recovery stage, which was shown by reduced synaptic protein levels on western blot. Early activations of glial cells and infiltrated monocytes demonstrating increased GFAP, Iba-1 and CD45 intensities on immunohistochemistry were also characteristic to 4KI mice. Interestingly, these apoE4-isoform depending changes were selective to hippocampus, not in motor cortex. Further, inverse correlation of microglial activations with number of neurons on immunohistochemistry and injured volume reduction on follow-up MRI was evident in hippocampus. This study demonstrates the effect of interaction between apoE4 and focal brain damage is specific to hippocampus. And it suggests that the delicate manipulation of inflammatory cell responses in hippocampus could be a strategy to diminish neurodegeneration and post-traumatic cognitive dysfunction in apoE4 carriers.
more목차
I. INTRODUCTION 1
II. MATERIALS AND METHODS 3
II-1. Mouse 3
II-2. Stereotaxic surgery 3
II-3. Magnetic resonance imaging (MRI) 4
II-4. Tissue preparation 5
II-5. Immunohistochemistry and analysis 6
II-6. Total protein extraction and Western blotting 8
II-7. Antibodies 9
II-8. Statistical Analysis 9
III. RESULTS 10
III-1. Serial check-up of focal brain damage in motor cortex and hippocampus using brain MRI 10
III-2. Isoform-dependent difference in synaptic protein levels in hippocampus during recovery from focal injury 16
III-3. Early increase of glial activity in hippocampus of 4KI mice after focal injury 19
III-4. Microglial conversion rate of monocytes in response to focal injury and correlation analysis 24
IV. DISCUSSIONS 29
REFERENCES 32
