Aït-Ikhlef A, Hantaz-Ambroise D, Henderson C E, Rieger F
INSERM Laboratoire de Neuromodulations Interactives et Neuropathologies, Paris, France.
J Neurosci Res. 2000 Jan 1;59(1):100-6.
During late postnatal development, mice with the autosomal recessive wobbler mutation (wr/wr) develop motoneuron degeneration associated with astrogliosis in the spinal cord. In vitro, primary wobbler astrocytes are also affected, exhibiting abnormal cell-cell contacts. To characterize further the wobbler disease, we investigated the in vitro effects of wobbler astrocytes on primary neuronal cultures from the spinal cords of 15-day-old wild-type mouse and rat embryos. Cocultures with the wobbler astrocytes, or direct addition of wobbler astrocyte-conditioned medium, led to a decrease in neuron number in primary mixed neuronal cultures, containing motoneurons and interneuron-like cells. In contrast, wobbler astrocyte-conditioned medium enhanced survival of highly purified motoneurons. These in vitro results suggest the possibility that wobbler astrocytes act not on motoneurons directly but, rather, through other spinal neurons to induce motoneuron degeneration in the wobbler disease.
在出生后晚期发育过程中,具有常染色体隐性震颤突变(wr/wr)的小鼠会发生运动神经元变性,并伴有脊髓星形胶质细胞增生。在体外,原代震颤星形胶质细胞也会受到影响,表现出异常的细胞间接触。为了进一步表征震颤疾病,我们研究了震颤星形胶质细胞对来自15日龄野生型小鼠和大鼠胚胎脊髓的原代神经元培养物的体外影响。与震颤星形胶质细胞共培养,或直接添加震颤星形胶质细胞条件培养基,会导致含有运动神经元和类中间神经元细胞的原代混合神经元培养物中的神经元数量减少。相比之下,震颤星形胶质细胞条件培养基可提高高度纯化的运动神经元的存活率。这些体外实验结果表明,震颤星形胶质细胞可能并非直接作用于运动神经元,而是通过其他脊髓神经元来诱导震颤疾病中的运动神经元变性。