Seeding cell number required for optimal lipid accumulation during adipocyte differentiation using 3T3-L1 cell line

Fuente: Zenodo
Saved in:
Bibliographic Details
Main Authors: Ariyanto, Eko Fuji, Odaiyappan, Naren A/L S., Lidyana, Lynna, Wikayani, Tenny Putri, Qomarilla, Nurul, Wira, Dwi Wahyudha, Triatin, Rima Destya
Format: Recurso digital
Language:English
Published: Zenodo 2019
Subjects:
Online Access:
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1866901745946329088
author Ariyanto, Eko Fuji
Odaiyappan, Naren A/L S.
Lidyana, Lynna
Wikayani, Tenny Putri
Qomarilla, Nurul
Wira, Dwi Wahyudha
Triatin, Rima Destya
author_facet Ariyanto, Eko Fuji
Odaiyappan, Naren A/L S.
Lidyana, Lynna
Wikayani, Tenny Putri
Qomarilla, Nurul
Wira, Dwi Wahyudha
Triatin, Rima Destya
contents <p><span lang="EN-US">Obesity is one of the major causes of metabolic diseases, such as diabetes and heart attack, and, hence, can lead to low quality of life<strong>. </strong>Elaborating adipocyte differentiation is very crucial for formulating the treatment and prevention of obesity. The objective of this study is to investigate the seeding cell number required to obtain optimum lipid accumulation during adipocyte differentiation using the 3T3-L1 cell line. </span><span lang="EN-US">Two sets of 5.48×10<sup>4</sup> (for Day 0 and Day 8 of differentiation), of 10.96×10<sup>4 </sup>(for Day 8) and of 21.92×10<sup>4</sup> (for Day 8) of 3T3-L1 cells were seeded in </span><span lang="EN-US">each</span><span lang="EN-US"> wells</span><span lang="EN-US"> of a 12-well plate. Isobuthylmethylxanthine (IBMX), Dexamethasone, and Insulin-containing differentiation cocktails were added into the medium at Day 0 for 48 hours. The medium was changed every two days. Day 0 and Day 8 samples were then stained using Oil Red O and were examined under the microscope to observe the lipid droplets (red-coloured). The lipid droplets were quantified by measuring the absorbance at wavelength of 550 nm.</span><span lang="EN-US"> In the study, s</span><span lang="EN-US">eeding the number of 10.96×10<sup>4</sup> </span><span lang="EN-US">cells produced very significantly higher lipid accumulation, as compared with seeding the number of 5.48×10<sup>4</sup> </span><span lang="EN-US">cells. However, doubling the seeding number into 21.92×10<sup>4 </sup>cells did not increase the lipid droplets significantly. This study found that the optimum seeding number to obtain the maximum lipid droplets during 3T3-L1 adipocyte differentiation was 10.96×10<sup>4</sup> cells.</span></p>
format Recurso digital
id zenodo_https___doi_org_10_5281_zenodo_19224848
institution Zenodo
language eng
publishDate 2019
publisher Zenodo
record_format zenodo
spellingShingle Seeding cell number required for optimal lipid accumulation during adipocyte differentiation using 3T3-L1 cell line
Ariyanto, Eko Fuji
Odaiyappan, Naren A/L S.
Lidyana, Lynna
Wikayani, Tenny Putri
Qomarilla, Nurul
Wira, Dwi Wahyudha
Triatin, Rima Destya
3T3-L1 preadipocytes, differentiation, lipid accumulation, seeding cell number
<p><span lang="EN-US">Obesity is one of the major causes of metabolic diseases, such as diabetes and heart attack, and, hence, can lead to low quality of life<strong>. </strong>Elaborating adipocyte differentiation is very crucial for formulating the treatment and prevention of obesity. The objective of this study is to investigate the seeding cell number required to obtain optimum lipid accumulation during adipocyte differentiation using the 3T3-L1 cell line. </span><span lang="EN-US">Two sets of 5.48×10<sup>4</sup> (for Day 0 and Day 8 of differentiation), of 10.96×10<sup>4 </sup>(for Day 8) and of 21.92×10<sup>4</sup> (for Day 8) of 3T3-L1 cells were seeded in </span><span lang="EN-US">each</span><span lang="EN-US"> wells</span><span lang="EN-US"> of a 12-well plate. Isobuthylmethylxanthine (IBMX), Dexamethasone, and Insulin-containing differentiation cocktails were added into the medium at Day 0 for 48 hours. The medium was changed every two days. Day 0 and Day 8 samples were then stained using Oil Red O and were examined under the microscope to observe the lipid droplets (red-coloured). The lipid droplets were quantified by measuring the absorbance at wavelength of 550 nm.</span><span lang="EN-US"> In the study, s</span><span lang="EN-US">eeding the number of 10.96×10<sup>4</sup> </span><span lang="EN-US">cells produced very significantly higher lipid accumulation, as compared with seeding the number of 5.48×10<sup>4</sup> </span><span lang="EN-US">cells. However, doubling the seeding number into 21.92×10<sup>4 </sup>cells did not increase the lipid droplets significantly. This study found that the optimum seeding number to obtain the maximum lipid droplets during 3T3-L1 adipocyte differentiation was 10.96×10<sup>4</sup> cells.</span></p>
title Seeding cell number required for optimal lipid accumulation during adipocyte differentiation using 3T3-L1 cell line
topic 3T3-L1 preadipocytes, differentiation, lipid accumulation, seeding cell number
url https://doi.org/10.5281/zenodo.19224848