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Modelling Functional Thyroid Follicular Structures Using P19 Embryonal Carcinoma Cells
by
Wei, Li-Na
, Najjar, Fatimah
, Wei, Chin-Wen
, Lerdall, Thomas
, Milbauer, Liming
in
Acids
/ Activin
/ Activins - metabolism
/ Activins - pharmacology
/ Analysis
/ Animals
/ Cancer
/ Carcinoma
/ Cell culture
/ Cell Differentiation
/ Cell Line, Tumor
/ Cellulose acetate
/ Embryoid Bodies - cytology
/ Embryoid Bodies - metabolism
/ embryonal carcinoma stem cells
/ Embryonal Carcinoma Stem Cells - metabolism
/ Embryonal Carcinoma Stem Cells - pathology
/ Endoderm
/ Follicles
/ Genes
/ Genetic engineering
/ Genetic transcription
/ Glycoproteins
/ Growth factors
/ Hormones
/ Hypothyroidism
/ in vitro models
/ Maturation
/ Medical research
/ Medicine, Experimental
/ Mice
/ Models, Biological
/ Molecular modelling
/ Physiology
/ Proteins
/ siRNA
/ Stem cells
/ Thyrocytes
/ Thyroglobulin
/ Thyroglobulin - metabolism
/ Thyroid carcinoma
/ Thyroid diseases
/ Thyroid Epithelial Cells - metabolism
/ Thyroid gland
/ Thyroid Gland - cytology
/ Thyroid Gland - metabolism
/ Thyroid-stimulating hormone
/ Thyrotropin - metabolism
/ Thyrotropin - pharmacology
/ Transcription factors
2024
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Modelling Functional Thyroid Follicular Structures Using P19 Embryonal Carcinoma Cells
by
Wei, Li-Na
, Najjar, Fatimah
, Wei, Chin-Wen
, Lerdall, Thomas
, Milbauer, Liming
in
Acids
/ Activin
/ Activins - metabolism
/ Activins - pharmacology
/ Analysis
/ Animals
/ Cancer
/ Carcinoma
/ Cell culture
/ Cell Differentiation
/ Cell Line, Tumor
/ Cellulose acetate
/ Embryoid Bodies - cytology
/ Embryoid Bodies - metabolism
/ embryonal carcinoma stem cells
/ Embryonal Carcinoma Stem Cells - metabolism
/ Embryonal Carcinoma Stem Cells - pathology
/ Endoderm
/ Follicles
/ Genes
/ Genetic engineering
/ Genetic transcription
/ Glycoproteins
/ Growth factors
/ Hormones
/ Hypothyroidism
/ in vitro models
/ Maturation
/ Medical research
/ Medicine, Experimental
/ Mice
/ Models, Biological
/ Molecular modelling
/ Physiology
/ Proteins
/ siRNA
/ Stem cells
/ Thyrocytes
/ Thyroglobulin
/ Thyroglobulin - metabolism
/ Thyroid carcinoma
/ Thyroid diseases
/ Thyroid Epithelial Cells - metabolism
/ Thyroid gland
/ Thyroid Gland - cytology
/ Thyroid Gland - metabolism
/ Thyroid-stimulating hormone
/ Thyrotropin - metabolism
/ Thyrotropin - pharmacology
/ Transcription factors
2024
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Modelling Functional Thyroid Follicular Structures Using P19 Embryonal Carcinoma Cells
by
Wei, Li-Na
, Najjar, Fatimah
, Wei, Chin-Wen
, Lerdall, Thomas
, Milbauer, Liming
in
Acids
/ Activin
/ Activins - metabolism
/ Activins - pharmacology
/ Analysis
/ Animals
/ Cancer
/ Carcinoma
/ Cell culture
/ Cell Differentiation
/ Cell Line, Tumor
/ Cellulose acetate
/ Embryoid Bodies - cytology
/ Embryoid Bodies - metabolism
/ embryonal carcinoma stem cells
/ Embryonal Carcinoma Stem Cells - metabolism
/ Embryonal Carcinoma Stem Cells - pathology
/ Endoderm
/ Follicles
/ Genes
/ Genetic engineering
/ Genetic transcription
/ Glycoproteins
/ Growth factors
/ Hormones
/ Hypothyroidism
/ in vitro models
/ Maturation
/ Medical research
/ Medicine, Experimental
/ Mice
/ Models, Biological
/ Molecular modelling
/ Physiology
/ Proteins
/ siRNA
/ Stem cells
/ Thyrocytes
/ Thyroglobulin
/ Thyroglobulin - metabolism
/ Thyroid carcinoma
/ Thyroid diseases
/ Thyroid Epithelial Cells - metabolism
/ Thyroid gland
/ Thyroid Gland - cytology
/ Thyroid Gland - metabolism
/ Thyroid-stimulating hormone
/ Thyrotropin - metabolism
/ Thyrotropin - pharmacology
/ Transcription factors
2024
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Modelling Functional Thyroid Follicular Structures Using P19 Embryonal Carcinoma Cells
Journal Article
Modelling Functional Thyroid Follicular Structures Using P19 Embryonal Carcinoma Cells
2024
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Overview
Thyroid gland diseases remain clinical challenges due to the lack of reliable in vitro models to examine molecular pathways of thyrocytes development, maturation, and functional maintenance. This study aimed to develop in vitro thyrocytes model using a stem cell culture, P19 embryonal carcinoma which requires no feeder layer, differentiation into mature and functional thyrocytes that allow molecular and genetic manipulation for studying thyroid diseases. The procedure utilizes Activin A and thyroid stimulating hormone (TSH) to first induce embryoid body endoderm formation enriched in thyrocyte progenitors. Following dissociating embryoid bodies, thyrocyte progenitors are plated in Matrigel as monolayer cultures that allows thyrocyte progenitors mature to functional thyrocytes. These thyrocytes further maturate to form follicle-like structures expressing and accumulating thyroglobulin that can be secreted into the medium upon TSH stimulation. Thyrocyte differentiation-maturation process is monitored by the expression of essential transcriptional factors and thyrocyte-specific functional genes. Further, the applicability of this system is validated by introducing a siRNA control. Following molecular manipulation, the system can still be guided to differentiate into mature and functional thyrocytes. This system spans a time frame of 14 days, suitable for detailed molecular studies to dissect pathways and molecular players in thyrocytes development and functional maintenance.
Publisher
MDPI AG,MDPI
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