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在ER81基因缺陷小鼠中,以高尔基腱器官为代价形成多余的肌梭。

Formation of supernumerary muscle spindles at the expense of Golgi tendon organs in ER81-deficient mice.

作者信息

Kucera J, Cooney W, Que A, Szeder V, Stancz-Szeder H, Walro J

机构信息

Department of Neurology, Boston University, 80 East Concord Street, Boston, MA 02118, USA.

出版信息

Dev Dyn. 2002 Mar;223(3):389-401. doi: 10.1002/dvdy.10066.

Abstract

ER81, a member of the ETS family of transcription factors, is essential for the formation of connections between sensory and motor neurons in the spinal cord. Mice lacking Er81 genes exhibit reduced monosynaptic sensory-motoneuron connectivity in response to muscle nerve stimulation. Proximal muscle nerve stimulation elicits fewer monosynaptic potentials than stimulation of distal nerves in hindlimbs, a deficit that is paralleled by a paucity of muscle spindles in proximal muscles (Arber et al., 2000). We examined whether a presence of spindles innervated by afferents in distal muscles correlated with the increased preservation of monosynaptic sensory-motor potentials in distal muscle nerves. Not only were spindles and Ia afferents present, but also they were supernumerary in distal muscles such as the soleus, medial gastrocnemius, and extensor hallucis longus. Concomitantly, a deficiency of Golgi tendon organs (GTOs) and Ib afferents was observed in distal muscles, as if supernumerary spindles formed at the expense of tendon organs in the absence of Er81. Thus, ER81 may be involved in mechanisms that regulate acquisition of the Ia and Ib phenotypes by subsets of proprioceptive muscle afferents. Segmental differences in muscle spindle and GTO dependence on ER81 suggest that more than one ETS transcription factor may participate in the regulation of limb proprioceptive system assembly in the mouse.

摘要

ER81是ETS转录因子家族的成员之一,对脊髓中感觉神经元和运动神经元之间连接的形成至关重要。缺乏Er81基因的小鼠在受到肌肉神经刺激时,单突触感觉运动神经元的连接性降低。近端肌肉神经刺激引发的单突触电位比后肢远端神经刺激引发的少,近端肌肉中肌梭数量的减少也存在类似缺陷(Arber等人,2000年)。我们研究了远端肌肉中由传入神经支配的肌梭的存在是否与远端肌肉神经中单突触感觉运动电位的更多保留相关。不仅存在肌梭和Ia传入神经,而且在比目鱼肌、内侧腓肠肌和拇长伸肌等远端肌肉中它们的数量还过多。同时,在远端肌肉中观察到高尔基腱器官(GTO)和Ib传入神经缺乏,就好像在没有Er81的情况下,过多的肌梭是以腱器官为代价形成的。因此,ER81可能参与了调节本体感受性肌肉传入神经亚群获得Ia和Ib表型的机制。肌肉梭和GTO对ER81的节段性差异表明,可能不止一种ETS转录因子参与了小鼠肢体本体感受系统组装的调节。

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