Huizinga J D, Thuneberg L, Klüppel M, Malysz J, Mikkelsen H B, Bernstein A
Department of Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada.
Nature. 1995 Jan 26;373(6512):347-9. doi: 10.1038/373347a0.
The pacemaker activity in the mammalian gut is responsible for generating anally propagating phasic contractions. The cellular basis for this intrinsic activity is unknown. The smooth muscle cells of the external muscle layers and the innervated cellular network of interstitial cells of Cajal, which is closely associated with the external muscle layers of the mammalian gut, have both been proposed to stimulate pacemaker activity. The interstitial cells of Cajal were identified in the last century but their developmental origin and function have remained unclear. Here we show that the interstitial cells of Cajal express the Kit receptor tyrosine kinase. Furthermore, mice with mutations in the dominant white spotting (W) locus, which have cellular defects in haematopoiesis, melanogenesis and gametogenesis as a result of mutations in the Kit gene, also lack the network of interstitial cells of Cajal associated with Auerbach's nerve plexus and intestinal pacemaker activity.
哺乳动物肠道中的起搏活动负责产生向肛门方向传播的阶段性收缩。这种内在活动的细胞基础尚不清楚。有人提出,外肌层的平滑肌细胞以及与哺乳动物肠道外肌层紧密相关的 Cajal 间质细胞的神经支配细胞网络,均可刺激起搏活动。Cajal 间质细胞于上世纪被发现,但其发育起源和功能仍不清楚。在此,我们表明 Cajal 间质细胞表达 Kit 受体酪氨酸激酶。此外,由于 Kit 基因突变导致造血、黑色素生成和配子发生存在细胞缺陷的显性白斑(W)位点突变小鼠,也缺乏与奥尔巴赫神经丛相关的 Cajal 间质细胞网络以及肠道起搏活动。