Department of Urology, Nihon University School of Medicine, Nihon University, Tokyo, Japan.
J Urol. 2009 Jul;182(1):355-65. doi: 10.1016/j.juro.2009.02.103. Epub 2009 May 20.
We recently reported that mature, adipocyte derived, dedifferentiated fat cells show high proliferative activity and multilineage differentiation potential. In the current study we investigated whether such cells could differentiate into a smooth muscle cell lineage and contribute to bladder tissue regeneration in a mouse bladder injury model.
Human adipocyte derived dedifferentiated fat cells were cultured for 1 week under conditions favorable for smooth muscle cell differentiation and immunostained for alpha-smooth muscle actin. The expression of smooth muscle cell marker genes for differentiating dedifferentiated fat cells was measured by real-time reverse transcription-polymerase chain reaction. Green fluorescence protein labeled dedifferentiated fat cells were injected into cryo-injured bladder walls in mice. The ability of the fat cells to regenerate smooth muscle tissue was examined immunohistochemically 14 and 30 days after transplantation.
Immunohistochemical analysis revealed that more than 50% of the fat cells were successfully differentiated into alpha-smooth muscle actin positive cells under the optimum culture condition of a medium containing 5% fetal bovine serum and 5 ng/ml transforming growth factor-beta1. Real-time reverse transcription-polymerase chain reaction revealed increased expression of SM22alpha, alpha-smooth muscle actin and smooth muscle-myosin heavy chain in dedifferentiated fat cells during week 1 of differentiation culture. Cells expressing alpha-smooth muscle actin plus green fluorescence protein were observed at the bladder wall injection sites in mice 14 and 30 days after transplantation. Alpha-smooth muscle actin positive areas in injured bladder tissue in mice with fat cell injection were significantly larger than those in saline injected control mice.
These findings suggest that dedifferentiated fat cells can differentiate into smooth muscle cell lineages and contribute to the regeneration of bladder smooth muscle tissue.
我们最近报道了成熟的脂肪细胞在去分化后具有高度的增殖活性和多能性分化潜能。在本研究中,我们研究了这些细胞是否能够分化为平滑肌细胞谱系,并在小鼠膀胱损伤模型中促进膀胱组织再生。
将人脂肪细胞来源的去分化脂肪细胞在有利于平滑肌细胞分化的条件下培养 1 周,并对α-平滑肌肌动蛋白进行免疫染色。通过实时逆转录聚合酶链反应测量分化的去分化脂肪细胞中平滑肌细胞标记基因的表达。将绿色荧光蛋白标记的去分化脂肪细胞注射到小鼠冷冻损伤的膀胱壁中。在移植后 14 和 30 天,通过免疫组织化学检查脂肪细胞再生平滑肌组织的能力。
免疫组织化学分析显示,在含有 5%胎牛血清和 5ng/ml 转化生长因子-β1 的培养基的最佳培养条件下,超过 50%的脂肪细胞成功分化为α-平滑肌肌动蛋白阳性细胞。实时逆转录聚合酶链反应显示,在分化培养的第 1 周,去分化脂肪细胞中 SM22α、α-平滑肌肌动蛋白和平滑肌肌球蛋白重链的表达增加。在移植后 14 和 30 天,在小鼠的膀胱壁注射部位观察到表达α-平滑肌肌动蛋白和绿色荧光蛋白的细胞。与生理盐水注射对照组相比,脂肪细胞注射小鼠的损伤膀胱组织中α-平滑肌肌动蛋白阳性区域明显更大。
这些发现表明,去分化脂肪细胞可以分化为平滑肌细胞谱系,并有助于膀胱平滑肌组织的再生。