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Study on the influence of substrate roughness on the development of E-cadherin junction in oral keratinocytes

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dc.contributor.advisor김현만-
dc.contributor.author김성표-
dc.date.accessioned2017-10-27T17:18:47Z-
dc.date.available2017-10-27T17:18:47Z-
dc.date.issued2017-08-
dc.identifier.other000000145555-
dc.identifier.urihttps://hdl.handle.net/10371/137224-
dc.description학위논문 (박사)-- 서울대학교 대학원 치의학대학원 치의과학과, 2017. 8. 김현만.-
dc.description.abstractJunctional epithelium (JE) may attach to the substrates with varying levels of roughness from a smooth crown surface to a root surface roughened due to various causes including periodontal treatments such as root planing. Since the physical property of substrates to which the epithelial cells attach may regulate the development of intercellular junctions, the development of intercellular junction between human gingival keratinocytes (HGKs) was studied on the rough substrates. HGKs were cultured on substrates with varying levels of roughness, which were prepared by rubbing hydrophobic polystyrene dishes with silicon carbide papers. The development of intercellular junctions was analyzed using scanning electron microscopy or confocal laser scanning microscopy after immunohistochemical staining of the cells for E-cadherin which organizes adherens junction, one of major intercellular junctions of oral keratinocytes. HGKs developed tight intercellular junctions devoid of wide intercellular gaps on smooth substrates and on rough substrates with low-nanometer dimensions (average roughness [Ra] = 121.3 ± 13.4 nm), although the ECJs of HGKs on rough substrates with low-nanometer dimensions developed later than those of HGKs on smooth substrates. In contrast, HGKs developed short intercellular junctions with wide intercellular gaps on rough substrates with mid- or high-nanometer dimensions (Ra = 505.3 ± 115.3 nm, 867.0 ± 168.6 nm). Notably, the stability of the ECJs was low on the rough substrates, as demonstrated by the rapid destruction of the cell junction following calcium depletion. Cortical actins developed at the cell membrane where ECJ did not develop. JNK activation promoted the development of cortical actins to regulate the development of ECJs in HGKs. In contrast, inhibition of JNK activity promoted ECJ development concomitant with the dissociation of cortical actins regardless of the levels of substrate roughness when HGKs were cultured at high density. These results indicate that the ECJs of HGKs develop slowly or defectively on the rough substrates with nanometer dimensions, and that this effect can be reversed by inhibiting JNK.-
dc.description.tableofcontents1. Introduction 1
1-1. Junctional epithelium 1
1-2. Epithelial attachments of junctional epithelium to tooth surface 2
1-3. Scaling and root planing 3
1-4. Effects of surface roughness on cell activity 4
1-5. E-cadherin junction 5
1-6. c-Jun N-terminal kinases 6
1-7. Purpose of the study 7
2. Material and Methods 9
2-1. Preparation of rough substrates 9
2-2. Reagents 11
2-3. Cell culture 12
2-4. Field emission scanning electron microscopic observation 12
2-5. Immunoblotting 12
2-6. Immunocytochemistry 13
2-7. Statistical analysis 14
3. Results 15
3-1. Limited and delayed spreading of oral keratinocytes on rough substrates 15
3-2. Defective intercellular junction development in HGKs cultured on rough substrates 16
3-3. Low stability of ECJs in cells cultured on rough substrates 19
3-4. Role of JNK in ECJ the development in HGKs cultured on rough surface 20
3-5. various F-actin bundles in ECJ development 22
4. Discussion 28
5. Conclusion 33
References 35
Tables 47
Figures and Legends 51
국문초록 76
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dc.formatapplication/pdf-
dc.format.extent3573243 bytes-
dc.format.mediumapplication/pdf-
dc.language.isoen-
dc.publisher서울대학교 대학원-
dc.subjectE-cadherin junctions-
dc.subjectCortical actins-
dc.subjectc-Jun N-terminal kinases-
dc.subjectGingival keratinocytes-
dc.subjectSubstrate roughness-
dc.subject.ddc617.6-
dc.titleStudy on the influence of substrate roughness on the development of E-cadherin junction in oral keratinocytes-
dc.typeThesis-
dc.contributor.AlternativeAuthorJin Chengbiao-
dc.description.degreeDoctor-
dc.contributor.affiliation치의학대학원 치의과학과-
dc.date.awarded2017-08-
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