Sago Ken, Tamahara Satoshi, Tomihari Mizuki, Matsuki Naoaki, Asahara Yukiho, Takei Akihiro, Bonkobara Makoto, Washizu Tsukimi, Ono Kenichiro
Department of Veterinary Clinical Pathobiology, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo, Japan.
J Vet Med Sci. 2008 Apr;70(4):353-7. doi: 10.1292/jvms.70.353.
To investigate in vitro differentiation of canine adipose tissue-derived stromal cells (ATSCs) into neuronal cells, ATSCs from celiac adipose tissue in clinically healthy beagle dogs were treated with 100 muM dibutyryl cyclic adenosine monophosphate (dbcAMP) and 125 muM isobuthylmethylxanthine (IBMX). ATSCs were morphologically changed into differentiated ATSCs from spindle-shaped cells to neuron-like cells with numerous processes after the treatment. Expression of neuron-specific enolase (NSE) as an early neuron specific marker protein was detected in both ATSCs and differentiated ATSCs, however diachronic increase of NSE expression was observed in differentiated ATSCs after the treatment with dbcAMP/IBMX. In addition, neurofilament-68 (NF-68) as an early to mature neuron specific marker protein was weakly expressed in differentiated ATSCs. Neuron specific glutamate and glucose transporter (EAAC1 and GLUT-3, respectively) mRNAs were strongly expressed in differentiated ATSCs compared with those in ATSCs, although glia specific glutamate transporter mRNA (GLT-1) was also detected in differentiated ATSCs. ATSCs can differentiate into early to mature neuronal cells and are candidate cells for autologous nerve regeneration therapy, although additional research is needed to examine functional characteristics of differentiated ATSCs.
为研究犬脂肪组织来源的基质细胞(ATSCs)在体外向神经元细胞的分化情况,对临床健康的比格犬腹腔脂肪组织中的ATSCs用100μM二丁酰环磷腺苷(dbcAMP)和125μM异丁基甲基黄嘌呤(IBMX)进行处理。处理后,ATSCs的形态从梭形细胞转变为具有许多突起的类神经元细胞,即分化的ATSCs。在ATSCs和分化的ATSCs中均检测到作为早期神经元特异性标志物蛋白的神经元特异性烯醇化酶(NSE)的表达,然而在用dbcAMP/IBMX处理后的分化的ATSCs中观察到NSE表达的历时性增加。此外,作为早期至成熟神经元特异性标志物蛋白的神经丝68(NF-68)在分化的ATSCs中弱表达。与ATSCs相比,神经元特异性谷氨酸和葡萄糖转运体(分别为EAAC1和GLUT-3)的mRNA在分化的ATSCs中强烈表达,尽管在分化的ATSCs中也检测到胶质细胞特异性谷氨酸转运体mRNA(GLT-1)。ATSCs可以分化为早期至成熟的神经元细胞,是自体神经再生治疗的候选细胞,不过还需要进一步研究来检测分化的ATSCs的功能特性。