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胶质细胞系源性神经营养因子可诱导肾上腺嗜铬细胞原代培养物中神经纤维的形成。

Glial-cell-line-derived neurotrophic factor induces nerve fibre formation in primary cultures of adrenal chromaffin cells.

作者信息

Förander P, Broberger C, Strömberg I

机构信息

Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden.

出版信息

Cell Tissue Res. 2001 Jul;305(1):43-51. doi: 10.1007/s004410100401.

Abstract

Neurotrophic factors, such as nerve growth factor (NGF), have been shown to promote the differentiation of neural crest neuroblasts into sympathetic neurons, whereas glucocorticoids promote the endocrine phenotype of adrenal medullary chromaffin cells. This pluripotency is preserved to some extent in adult chromaffin cells, with NGF and other neurotrophic factors influencing the differentiation of these cells. In this study, the effects of glial cell line-derived neurotrophic factor (GDNF) on explanted chromaffin tissue have been investigated. The localization of mRNAs corresponding to the two components of the GDNF receptor, GDNF family receptor alpha 1 (GFRalpha1) and Ret, were demonstrated in adult adrenal medullary ganglion cells. GFRalpha1 mRNA was expressed in explanted chromaffin tissue at levels dependent on the presence of serum in the medium but decreased on the addition of blocking antibodies against transforming growth factor beta (TGFbeta). However, TGFbeta1 (1 ng/ml) did not upregulate GFRalpha1 mRNA expression when added to serum-free medium. GDNF induced neurite formation from chromaffin cells, as measured by the ratio of neurite-bearing versus total number of chromaffin cells in primary cultures of adult adrenal medulla. The most potent dose inducing neurites from chromaffin cells was 100 ng/ml GDNF. However, this dose was not as efficient as that seen when chromaffin cells were stimulated with NGF (100 ng/ml). Thus, adrenal medullary cells express mRNAs for the GDNF receptor components Ret and GFRalpha1, increase their expression upon being cultured in serum-containing medium and respond to GDNF treatment with an increase in the number of cells that develop nerve processes.

摘要

神经营养因子,如神经生长因子(NGF),已被证明可促进神经嵴神经母细胞分化为交感神经元,而糖皮质激素则促进肾上腺髓质嗜铬细胞的内分泌表型。这种多能性在成年嗜铬细胞中在一定程度上得以保留,NGF和其他神经营养因子会影响这些细胞的分化。在本研究中,研究了胶质细胞系源性神经营养因子(GDNF)对体外培养的嗜铬组织的影响。在成年肾上腺髓质神经节细胞中证实了与GDNF受体的两个组分,即GDNF家族受体α1(GFRα1)和Ret相对应的mRNA的定位。GFRα1 mRNA在体外培养的嗜铬组织中的表达水平取决于培养基中血清的存在,但在添加抗转化生长因子β(TGFβ)的阻断抗体后会降低。然而,当将TGFβ1(1 ng/ml)添加到无血清培养基中时,它并没有上调GFRα1 mRNA的表达。通过成年肾上腺髓质原代培养物中带有神经突的嗜铬细胞与嗜铬细胞总数的比率来衡量,GDNF诱导嗜铬细胞形成神经突。诱导嗜铬细胞形成神经突的最有效剂量是100 ng/ml GDNF。然而,该剂量不如用NGF(100 ng/ml)刺激嗜铬细胞时有效。因此,肾上腺髓质细胞表达GDNF受体组分Ret和GFRα1的mRNA,在含血清培养基中培养时其表达增加,并且对GDNF处理有反应,形成神经突起的细胞数量增加。

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