Church Christopher, Brown Mallory, Rodeheffer Matthew S
Section of Comparative Medicine; School of Medicine; Yale University ; New Haven, CT, USA.
Department of Molecular; Cell and Developmental Biology; School of Medicine; Yale University ; New Haven, CT, USA.
Adipocyte. 2015 Jan 20;4(3):203-11. doi: 10.1080/21623945.2014.995510. eCollection 2015 Jul-Sep.
The production of new adipocytes requires the differentiation of adipocyte precursor (AP) cells residing within the adipose tissue stromal-vascular compartment. The objective was to obtain an immortalized primary adipogenic cell line derived from FACS isolated committed APs using the conditional expression of SV40 T antigen. Adipocyte precursors were isolated from white adipose tissue (WAT) using FACS to remove non-adipogenic cell populations from mice expressing a conditionally regulated SV40 T antigen. APs were maintained by continuous culture and induced to undergo adipogenic differentiation. Adipogenesis, determined by Oil Red O staining, was assessed with each passage and compared to wildtype controls. Adipogenic capability was rapidly lost with increased passage number in committed APs with concurrent reduction in cell proliferation and expression of essential late adipogenic genes, including Pparγ and C/ebpα. Thus, FACS purified committed APs have limited capability to undergo expansion and subsequent adipogenic differentiation in vitro even if they are immortalized with the SV40 T antigen.
新脂肪细胞的产生需要脂肪组织基质血管隔室内的脂肪细胞前体(AP)细胞进行分化。目的是利用SV40 T抗原的条件性表达,从经荧光激活细胞分选(FACS)分离的定向AP中获得永生化的原代脂肪生成细胞系。使用FACS从小鼠白色脂肪组织(WAT)中分离脂肪细胞前体,以去除表达条件性调控的SV40 T抗原的小鼠中的非脂肪生成细胞群体。通过连续培养维持AP,并诱导其进行脂肪生成分化。每次传代时通过油红O染色测定脂肪生成,并与野生型对照进行比较。在定向AP中,随着传代次数增加,脂肪生成能力迅速丧失,同时细胞增殖以及包括过氧化物酶体增殖物激活受体γ(Pparγ)和CCAAT增强子结合蛋白α(C/ebpα)在内的关键晚期脂肪生成基因的表达也随之降低。因此,即使经FACS纯化的定向AP用SV40 T抗原永生化,其在体外进行扩增和随后脂肪生成分化的能力也有限。