Cell division and apoptosis in the adult neural stem cell niche are differentially affected in transthyretin null mice

Autor: Zahra Hassani, Barbara A. Demeneix, Samantha J. Richardson, Gregory F. Lemkine, Gladys Alfama
Přispěvatelé: Department of Epidemiology and Public Health, Imperial College Norfolk Place, Evolution des régulations endocriniennes (ERE), Muséum national d'Histoire naturelle (MNHN)-Centre National de la Recherche Scientifique (CNRS)
Jazyk: angličtina
Rok vydání: 2007
Předmět:
MESH: Cell Differentiation
medicine.medical_specialty
Programmed cell death
endocrine system
Cell division
Tyrosine 3-Monooxygenase
MESH: Neurons
Subventricular zone
Apoptosis
MESH: Stem Cells
Biology
MESH: Mice
Knockout

Cerebral Ventricles
03 medical and health sciences
Mice
0302 clinical medicine
Internal medicine
MESH: Prealbumin
medicine
Animals
Prealbumin
MESH: Animals
[SDV.BBM]Life Sciences [q-bio]/Biochemistry
Molecular Biology

Progenitor cell
MESH: Tyrosine 3-Monooxygenase
MESH: Mice
030304 developmental biology
Mice
Knockout

Neurons
0303 health sciences
General Neuroscience
Stem Cells
MESH: Apoptosis
nutritional and metabolic diseases
Cell Differentiation
Neural stem cell
Transthyretin
medicine.anatomical_structure
Endocrinology
nervous system
biology.protein
MESH: Cell Division
Choroid plexus
MESH: Cerebral Ventricles
Stem cell
030217 neurology & neurosurgery
Cell Division
Zdroj: Neuroscience Letters
Neuroscience Letters, Elsevier, 2007, 421 (3), pp.234-8. ⟨10.1016/j.neulet.2007.05.040⟩
ISSN: 0304-3940
DOI: 10.1016/j.neulet.2007.05.040⟩
Popis: Thyroid hormones (THs) are fundamental in regulation of growth and development, particularly of the brain. THs are required for full proliferative activity of neural stem cells in the subventricular zone (SVZ) of adult mouse brains, and also affect the normal fate of progenitor cells: apoptosis. Transthyretin (TTR) is a TH distributor protein in the blood and cerebrospinal fluid. TTR secretion by the choroid plexus is involved in transport of THs from blood into cerebrospinal fluid. We investigated the regulation of neural stem cell cycle in the SVZ of adult TTR null mice. Markers for neural stem cell mitosis that are reduced during hypothyroidism, did not differ between genotypes. However, in TTR null mice the level of apoptosis, the fate of most progenitor cells, was as low as that in brains of hypothyroid wildtype mice. Thus, lack of TTR results in reduced availability of TH to progenitor cells in the SVZ. We show that proliferation and apoptosis in the SVZ neural stem cell niche are differentially affected by the lack of TTR synthesis.
Databáze: OpenAIRE