Functional consequences of myeloid cell-specific Stat3 activation in skin fibrosis:
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1. Verfasser: | |
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Format: | Abschlussarbeit Buch |
Sprache: | English |
Veröffentlicht: |
Köln
2017
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Online-Zugang: | Inhaltsverzeichnis Inhaltsverzeichnis |
Beschreibung: | 91 Seiten Illustrationen 21 cm |
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Datensatz im Suchindex
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adam_text | TABLE OF CONTENT
ZUSAMMENFASSUNG
SUMMARY
TABLE OF FIGURES
TABLE OF TABLES
1
INTRODUCTION..................................................................................................................
-1 -
1.1 SKIN ARCHITECTURE AND FUNCTION
.............................................................................
-1 -
1.1.1 EXTRACELLULAR
MATRIX.......................................................................................-
2 -
1.2 SKIN
FIBROSIS...........................................................................................................
- 5 -
1.2.1 CUTANEOUS WOUND HEALING IN
PHYSIOLOGY..................................................- 5 -
1.2.2 IMPAIRED WOUND HEALING AND PATHOLOGICAL FIBROTIC RESPONSES
..............
- 7 -
1.2.3 MOUSE MODEL OF BLEOMYCIN-INDUCED SKIN FIBROSIS
...................................
- 8 -
1.2.4 THE ROLE OF MACROPHAGES IN SKIN REPAIR AND FIBROSIS
.............................
- 9 -
1.3
MACROPHAGES.......................................................................................................-10-
1.3.1 MACROPHAGE ORIGIN AND
IDENTIFICATION......................................................-1 0
-
1.3.2 MACROPHAGE FUNCTION
..................................................................................
-11-
1.3.3 MACROPHAGE ACTIVATION AND NOMENCLATURE
............................................
-1 2 -
1.3.4 TOLL-LIKE RECEPTOR 4 SIGNALING-MEDIATED INFLAMMATORY RESPONSE
...........
-1 3 -
1.4 CYTOKINES, GROWTH FACTORS AND THEIR SIGNALING PATHWAYS
............................
-1 4 -
1.4.1 P38A M
ARK.................................................................................................
-14-
1.4.2 SIGNAL TRANSDUCER AND ACTIVATOR OF TRANSCRIPTION 3 (STAT3)
....................
-15-
1.4.3 TRANSFORMING GROWTH FACTOR SS (TG
FSS)......................................................- 20 -
2
AIMS.............................................................................................................................
-23-
3
RESULTS.........................................................................................................................-24-
3.1 EFFICIENT GENE DELETION AND IMPAIRED PROTEIN ACTIVATION IN P38AMKO
OR STAT3MKO
MICE
3.2 SKIN INJURY AND ACUTE WOUND HEALING MOUSE MODEL
-24-
-26-
3.2.1 MYELOID CELL-RESTRICTED P38A DEFICIENCY HAS NO MAJOR IMPACT ON
WOUND
MORPHOLOGY AND KINETICS OF SKIN
REPAIR..................................................................-
26 -
3.2.2 MYELOID CELL-RESTRICTED STAT3 DEFICIENCY HAS NO MAJOR IMPACT ON
WOUND
MORPHOLOGY AND KINETICS OF SKIN
REPAIR..................................................................-
32 -
3.3 BLEOMYCIN-INDUCED SKIN FIBROSIS MOUSE
MODEL.............................................- 36 -
3.3.1 MYELOID CELL-SPECIFIC STAT3 DEFICIENCY ACCELERATES THE DEVELOPMENT
OF
BLEOMYCIN-INDUCED SKIN FIBROSIS
..............................................................................
- 36 -
3.3.2 MYELOID CELL-RESTRICTED STAT3 DEFICIENCY INCREASES COLLAGEN
DEPOSITION IN
BLEOMYCIN-INDUCED FIBROTIC
LESIONS..........................................................................-
37 -
3.3.3 ENHANCED FIBROSIS IN STAT3MK0 MICE IS CHARACTERIZED BY INCREASED
SMAD2
PHOSPHORYLATION AND COMP EXPRESSION
...............................................................
-41 -
3.3.4 MYELOID CELL-SPECIFIC STAT3 DEFICIENCY LEADS TO AUGMENTED MAST
CELL
NUMBERS AT THE FIBROTIC EDGE OF THE BLEOMYCIN-INDUCED LESION
.........................
- 42 -
3.3.5 STAT3-DEFICIENT MACROPHAGES FROM THE FIBROTIC LESION ARE
DIFFERENTLY
ACTIVATED AND EXPRESS LESS ANTI-FIBROTIC MEDIATORS
..............................................
- 44 -
3.3.6 DECORIN EXPRESSION IS NOT REDUCED IN THE OVERALL FIBROTIC LESION
OF STAT3MKO
MICE IN
VIVO.................................................................................................................-
45 -
3.3.7 IL-10 INCREASES SOCS3 EXPRESSION AND REPRESSES TGFSS PRODUCTION IN
BMDMS VIA STAT3 SIGNALING IN
VITRO.........................................................................-
46 -
3.3.6 IL-10 STIMULATED MACROPHAGES CONTROL THE EXPRESSION OF CTGF IN
FIBROBLASTS IN
VITRO.......................................................................................................
- 49 -
4
DISCUSSION....................................................................................................................
-50-
4.1 P38AMKO MICE SHOW AN INCREASED NUMBER OF NEUTROPHILS IN THE EARLY
WOUND
TISSUE, YET SHOW NO MAJOR WOUND HEALING
PHENOTYPE.............................................- 50 -
4.2 STAT3MKO MICE HAVE DIFFERENTLY ACTIVATED WOUND MACROPHAGES, YET SHOW
NO
MAJOR WOUND HEALING PHENOTYPE
.................................................................................
- 51 -
4.3 MYELOID CELL-RESTRICTED STAT3 DEFICIENCY ACCELERATES THE DEVELOPMENT
OF
BLEOMYCIN-INDUCED SKIN FIBROSIS
..................................................................................
- 52 -
4.3.1 STAT3 RESTRICTS THE AUTOCRINE TGFSS LOOP IN MACROPHAGES, THUS
LIMITING
TGFSS AVAILABILITY AND PRO-FIBROTIC FIBROBLAST ACTIVATION
.......................................
- 52 -
4.3.2 IMPAIRED DECORIN EXPRESSION IN MACROPHAGES DOES NOT REDUCE THE
TOTAL
AMOUNT OF DECORIN IN BLEOMYCIN-INDUCED FIBROTIC SKIN
........................................
- 54 -
4.3.3 ACCELERATED FIBROSIS DEVELOPMENT IN STAT3MK0 MICE IS INDEPENDENT
FROM
PRO-INFLAMMATORY CYTOKINE EXPRESSION IN MACROPHAGES
...................................
- 55 -
4.3.4 HOW MUCH DO ECM DEGRADATION AND PROTEOLYTIC ACTIVATION OF TGFSS
CONTRIBUTE TO THE FIBROTIC
PHENOTYPE?.....................................................................-
56 -
4.4
PERSPECTIVE...........................................................................................................-57-
5 MATERIALS AND
METHODS.............................................................................................-
60 -
5.1 REAGENTS AND BUFFERS
........................................................................................
- 60 -
5.2 EXPERIMENTAL
ANIMALS.........................................................................................-
61 -
5.2.1 MOUSE STRAINS (P38AMKO, STAT3MK0, TGFSSRIIMK0)
................................
-61 -
5.2.2
GENOTYPING...................................................................................................
-61-
5.2.2.1 ISOLATION OF GENOMIC
DMA.....................................................................-
61 -
5.2.2.2 P C R
.........................................................................................................
-62-
5.2.3
WOUNDING.....................................................................................................
-63-
5.2.3.1 FULL-THICKNESS SKIN EXCISIONAL
WOUNDING...........................................- 63 -
5.2.3 2 BLEOMYCIN-INDUCED SKIN
FIBROSIS......................................................... - 63 -
5.3
HISTOLOGY...............................................................................................................-64-
5.3.1
HISTOCHEMISTRY.............................................................................................
-64-
5.3.2 I MM U
NOHISTOCHEMISTRY................................................................................-
64 -
5.3.3 MORPHOMETRIC
ANALYSIS................................................................................-
66 -
5.3.3.1 SIRIUS
RED................................................................................................-
66 -
5.3.3.2 SECOND HARMONIC GENERATION MICROSCOPY
.......................................
- 66 -
5.4 CELL ISOLATION FROM
TISSUE...................................................................................
- 67 -
5.4.1 FLUORESCENCE ACTIVATED CELL SORTING (FACS)
...........................................
- 67 -
5.4.1 ISOLATION OF PRIMARY
FIBROBLASTS..................................................................-
69 -
5.4.2 ISOLATION OF MACROPHAGES ( M 0 )
................................................................- 69 -
5.4.2.1 PERITONEAL EXUDATE CELLS/ PERITONEAL MACROPHAGES
........................
- 69 -
S.4.2.2 BONE-MARROW DERIVED MACROPHAGES (BM DM S)
.............................
-6 9
5.5 CELL
CULTURE...........................................................................................................-
70
5.5.1 CULTURE OF PRIMARY
MACROPHAGES.............................................................-7
0
5.5.1 CULTURE OF PRIMARY
FIBROBLASTS....................................................................-
71
5.5.2 TRANS-WELL CO-CULTURE OF MACROPHAGES AND
FIBROBLASTS.......................-71
5.6 ENZYME-LINKED IMMUNOSORBENT ASSAY (ELISA) FOR TGFSS DETECTION
........
-7 2
5.7 RNA EXTRACTION, REVERSE TRANSCRIPTION PCR AND
QRT-PCR........................- 72
5.8 WESTERN
BLOT........................................................................................................
- 75
5.9 STATISTICAL
ANALYSIS..............................................................................................
- 76
6
REFERENCES..................................................................................................................-
77
7
ABBREVIATIONS.............................................................................................................
-8 6
6
ACKNOWLEDGEMENTS...................................................................................................-
90
9 EIDESSTATTLICHE
ERKLAERUNG.........................................................................................
- 91
|
any_adam_object | 1 |
author | Do, Nhu-Nguyen |
author_GND | (DE-588)1125143614 |
author_facet | Do, Nhu-Nguyen |
author_role | aut |
author_sort | Do, Nhu-Nguyen |
author_variant | n n d nnd |
building | Verbundindex |
bvnumber | BV044465056 |
ctrlnum | (OCoLC)990781560 (DE-599)DNB1131738160 |
discipline | Medizin |
format | Thesis Book |
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spelling | Do, Nhu-Nguyen Verfasser (DE-588)1125143614 aut Functional consequences of myeloid cell-specific Stat3 activation in skin fibrosis vorgelegt von Nhu-Nguyen Do Köln 2017 91 Seiten Illustrationen 21 cm txt rdacontent n rdamedia nc rdacarrier Dissertation Universität zu Köln 2017 (DE-588)4113937-9 Hochschulschrift gnd-content B:DE-101 application/pdf http://d-nb.info/1131738160/04 Inhaltsverzeichnis DNB Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=029865631&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis |
spellingShingle | Do, Nhu-Nguyen Functional consequences of myeloid cell-specific Stat3 activation in skin fibrosis |
subject_GND | (DE-588)4113937-9 |
title | Functional consequences of myeloid cell-specific Stat3 activation in skin fibrosis |
title_auth | Functional consequences of myeloid cell-specific Stat3 activation in skin fibrosis |
title_exact_search | Functional consequences of myeloid cell-specific Stat3 activation in skin fibrosis |
title_full | Functional consequences of myeloid cell-specific Stat3 activation in skin fibrosis vorgelegt von Nhu-Nguyen Do |
title_fullStr | Functional consequences of myeloid cell-specific Stat3 activation in skin fibrosis vorgelegt von Nhu-Nguyen Do |
title_full_unstemmed | Functional consequences of myeloid cell-specific Stat3 activation in skin fibrosis vorgelegt von Nhu-Nguyen Do |
title_short | Functional consequences of myeloid cell-specific Stat3 activation in skin fibrosis |
title_sort | functional consequences of myeloid cell specific stat3 activation in skin fibrosis |
topic_facet | Hochschulschrift |
url | http://d-nb.info/1131738160/04 http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=029865631&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |
work_keys_str_mv | AT donhunguyen functionalconsequencesofmyeloidcellspecificstat3activationinskinfibrosis |
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