分子生物学
IVD分子诊断
细胞培养与分析
蛋白研究
细胞因子
重组蛋白
抗体
高通量测序建库
病原检测UCF系列
生物医药
工具酶
抑制剂激活剂与常用试剂
仪器
耗材

Cell cytoskeleton and proliferation study for the RANKL-induced RAW264.7 differentiation

Lingbo Kong, Rui Ma, Yang Cao, Wanli Smith, Yuan Liu, Xiaobin Yang, Liang Yan

Journal:JOURNAL OF CELLULAR AND MOLECULAR MEDICINE

IF:5.31

DOI:10.1111/jcmm.16390

PMID:33742541

Published:2021-03-19

research field:肿瘤学分子生物学药理学细胞生物学

Abstract

Although document studies (including ours) have been reported the achieved in vitro osteoclastic cellular model establishment from the RAW264.7 cell lineage, there was no study directly reported that American Type Culture Collection (ATCC) cell bank has various RAW264.7 cell lineages. Besides that, for our knowledge there was only one study compared the two different RAW264.7 TIB-71 and RAW264.7 CRL-2278 cell lineages for their osteoclastic differentiation, and they concluded that the RAW264.7 CRL-2278 demonstrated to generate much osteoclast than RAW264.7 TIB-71 . However, on the contrary to their results we noticed the fusion of RAW264.7 TIB-71 in our previous studies was much compromising. Therefore, we try to explore the two cell lineages for their properties in osteoclastic differentiation with an in-depth cellular cytoskeletal study. Our current study has showed that comparing to the RAW264.7 CRL-2278 , RAW264.7 TIB-71 demonstrated a much higher efficacies for RANKL-stimulated osteoclastic differentiation. Besides that, in our depth cytoskeletal studies, we found that the RANKL-induced RAW264.7 TIB-71 cells could finally differentiate into mature osteoclasts. However, regardless the various pre-treatment conditions, there was no mature osteoclast formed in RANKL-induced RAW264.7 CRL-2278 cell lineage.

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