Faculty Opinions recommendation of TAK1 regulates SOX9 expression in chondrocytes and is essential for postnatal development of the growth plate and articular cartilages.

Estrogen regulates skeletal growth and promotes epiphyseal fusion. To explore the mechanisms underlying these effects we investigated the expression of estrogen receptor-alpha (ERalpha) and -beta (ERbeta) in rat and rabbit growth plates during postnatal development, using immunohistochemistry. Immunoreactivity for ERalpha and ERbeta was observed in resting zone and proliferative zone chondrocytes at all ages studied for both rat (7, 14, 28 and 70 days of age) and rabbit (1, 7, 28 and 120 days of age). In the rat distal humerus and the rabbit proximal tibia, expression of both receptors in the hypertrophic zone was minimal at early ages, increasing only at the last time point prior to epiphyseal fusion. Expression was rarely seen in the hypertrophic zone of the rat proximal tibia, a growth plate that does not fuse until late in life. Therefore, we conclude that ERalpha and ERbeta are both expressed in the mammalian growth plate. The temporal and anatomical pattern suggests that ER expression in the hypertrophic zone in particular may play a role in epiphyseal fusion.

Download Full-text

Review for "Postnatal Development of the Entorhinal Cortex: A Stereological Study in Macaque Monkeys"

10.1002/cne.24897/v2/review2 ◽

2020 ◽

Author(s):

Takashi Kitamura

Keyword(s):

Postnatal Development ◽

Entorhinal Cortex ◽

Macaque Monkeys

Download Full-text

Review for "Postnatal Development of the Entorhinal Cortex: A Stereological Study in Macaque Monkeys"

10.1002/cne.24897/v2/review1 ◽

2020 ◽

Author(s):

Ricardo Insausti

Keyword(s):

Postnatal Development ◽

Entorhinal Cortex ◽

Macaque Monkeys

Download Full-text

Effects of Hypophysectomy on the Occurrence and Calcifiability of Matrix Vesicles in the Epiphyseal Growth Plate of Immature Rats

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s1431927600002579 ◽

1980 ◽

Vol 38 ◽

pp. 578-579

Author(s):

S. I. Coleman ◽

W. J. Dougherty

Keyword(s):

Growth Plate ◽

Matrix Vesicles ◽

Epiphyseal Growth Plate ◽

Hard Tissue ◽

Hormonal Factors ◽

Post Surgery ◽

Mineral Deposition ◽

Thin Sectioning ◽

Integral Role ◽

Cellular Secretion

In the cellular secretion theory of mineral deposition, extracellular matrix vesicles are believed to play an integral role in hard tissue mineralization (1). Membrane limited matrix vesicles arise from the plasma membrane of epiphyseal chondrocytes and tooth odontoblasts by a budding process (2, 3). Nutritional and hormonal factors have been postulated to play essential roles in mineral deposition and apparently have a direct effect on matrix vesicles of calcifying cartilage as concluded by Anderson and Sajdera (4). Immature (75-85 gm) Long-Evans hooded rats were hypophysectomized by the parapharyngeal approach and maintained fourteen (14) days post-surgery. At this time, the animals were anesthetized and perfusion fixed in cacodylate buffered 2.5% glutaraldehyde. The proximal tibias were quickly dissected out and split sagittally. One half was used for light microscopy (LM) and the other for electron microscopy (EM). The halves used for EM were cut into blocks approximately 1×3 mm. The tissue blocks were prepared for ultra-thin sectioning and transmission EM. The tissue was oriented so as to section through the epiphyseal growth plate from the zone of proliferating cartilage on down through the hypertrophic zone and into the initial trabecular bone. Sections were studied stained (double heavy metal) and unstained.

Download Full-text