𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Thyroid hormone stimulates adipocyte differentiation of 3T3 cells

✍ Scribed by Guillermo Flores-Delgado; Meytha Marsch-Moreno; Walid Kuri-Harcuch


Publisher
Springer
Year
1987
Tongue
English
Weight
609 KB
Volume
76
Category
Article
ISSN
0300-8177

No coin nor oath required. For personal study only.

✦ Synopsis


Triiodothyronine added at 0.1 nM to 3T3-F442A cells cultured in adipogenic medium having endogenous hormone concentrations similar to those of hypothyroid serum stimulated adipose conversion; activities of both lipogenic enzymes, glycerophosphate dehydrogenase and malic enzyme, increased with hormone treatment. The number of adipocytes was also augmented by L-T3 addition but the number of fat cell clusters remained the same as compared to non-treated cultures, suggesting that thyroid hormone increased the number of adipocytes probably through stimulating selective multiplication of precursor adipose cells. Hormone addition to cells cultured with non-adipogenic medium did not promote conversion showing that L-T3 is not an adipogenic factor by itself. Triiodothyronine added at concentrations similar to those found in hyperthyroidism, from 10 nM up to 10 microM, also increased the proportion of adipocytes without changing the number of fat cell clusters, but they decreased the activity of both lipogenic enzymes and lipid accumulation in mature adipocytes. It can be concluded that during 3T3-F442A differentiation into adipocytes L-T3 increases the number of differentiated adipocytes and, at low concentrations, also enhances lipogenic enzyme activities, whereas at the hyperthyroid hormone levels these enzyme activities are significantly reduced, remaining at levels similar to those of cells cultured with hypothyroid medium. This cloned cell line seems to be a useful model to study thyroid hormone action at both molecular and cellular level.


πŸ“œ SIMILAR VOLUMES


Sex steroid hormones induce acylation st
✍ Yu Wen; HongWei Wang; Robin MacLaren; HuiLing Lu; Xiu-Fen Hu; Katherine Cianflon πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons 🌐 English βš– 400 KB

## Abstract Acylation stimulating protein (ASP) stimulates triglyceride synthesis and glucose transport via its receptor C5L2. In human studies, ASP is increased in insulin resistant states such as obesity, diabetes, polycystic ovary syndrome and late pregnancy (the latter two associated with alter

Heparin potentiation of 3T3-adipocyte st
✍ John J. Castellot Jr.; Arbetta M. Kambe; Deborah E. Dobson; Bruce M. Spiegelman πŸ“‚ Article πŸ“… 1986 πŸ› John Wiley and Sons 🌐 English βš– 845 KB

We have examined the cellular mechanisms by which heparin potentiates the ability of 3T3-adipocytes to stimulate the formation of new blood vessels. Both anticoagulant and non-anticoagulant heparin species enhanced the angiogenic activity of adipocyte-secreted products in the chick chorioallantoic m

Cholera toxin stimulates division of 3T3
✍ Rebecca M. Pruss; Harvey R. Herschman πŸ“‚ Article πŸ“… 1979 πŸ› John Wiley and Sons 🌐 English βš– 424 KB

## Abstract Cholera toxin was used in an attempt to inhibit epidermal growth factor stimulated 3T3 cell division. Instead, cholera toxin alone at low concentrations (10^βˆ’10^ M), was able to stimulate cell division and could augment EGF stimulated cell division. The mitogenic effect of cholera toxin

Signaling pathways implicated in Ξ±-melan
✍ Kyung-Joo Cho; Jung-Hyun Shim; Min-Chul Cho; Yong-Kyung Choe; Jin-Tae Hong; Dong πŸ“‚ Article πŸ“… 2005 πŸ› John Wiley and Sons 🌐 English βš– 228 KB

## Abstract Melanocortins, besides their central roles, have also recently been reported to regulate adipocyte metabolism. In this study, we attempted to characterize the mechanism underlying α‐melanocyte‐stimulating hormone (MSH)‐induced lipolysis, and compared it with that of the adrenocorticotro

Ξ²-cryptoxanthin stimulates cell differen
✍ Satoshi Uchiyama; Masayoshi Yamaguchi πŸ“‚ Article πŸ“… 2005 πŸ› John Wiley and Sons 🌐 English βš– 431 KB

## Abstract The effect of β‐cryptoxanthin, a kind of carotenoid, on cell differentiation and mineralization in osteoblastic MC3T3‐E1 cells was investigated. Cells were cultured for 72 h in a minimum essential medium containing 10% fetal bovine serum (FBS), and the cells with subconfluency were chan