Hertzberg T, Fan G, Finley J C, Erickson J T, Katz D M
Department of Neurosciences, Case Western Reserve University, School of Medicine, Cleveland, Ohio 44106-4975.
Dev Biol. 1994 Dec;166(2):801-11. doi: 10.1006/dbio.1994.1358.
Chemoreceptor neurons innervating the rat carotid body were used as a model system to define target regulation of visceral sensory development in fetal and newborn animals. In vitro, chemoafferents were selectively supported by coculture with the carotid body or by treatment with trkB ligands [brain-derived neurotrophic factor (BDNF) and neurotrophin-4], whereas nerve growth factor and neurotrophin 3 had no effect. In vivo, chemoafferent neurons died following carotid body removal at birth, indicating a predominant role of peripheral, rather than central, targets in mediating survival at this stage. However, in the absence of target tissues, a large proportion of carotid body afferents could be rescued by implants containing BDNF. Moreover, BDNF mRNA was detected in the newborn carotid body by reverse transcriptase polymerase chain reaction. These data provide the first demonstration that BDNF can substitute for peripheral target support of sensory neuron survival in vivo and indicate that trkB ligands may be particularly important for development of visceral afferents involved in cardiorespiratory control.
支配大鼠颈动脉体的化学感受器神经元被用作模型系统,以确定胎儿和新生动物内脏感觉发育的靶标调控。在体外,化学传入神经通过与颈动脉体共培养或用trkB配体[脑源性神经营养因子(BDNF)和神经营养素-4]处理而得到选择性支持,而神经生长因子和神经营养素3则没有作用。在体内,出生时切除颈动脉体后化学传入神经元死亡,表明在此阶段外周而非中枢靶标在介导存活中起主要作用。然而,在没有靶组织的情况下,很大一部分颈动脉体传入神经可以通过含有BDNF的植入物得到挽救。此外,通过逆转录聚合酶链反应在新生大鼠颈动脉体中检测到BDNF mRNA。这些数据首次证明BDNF可以替代体内感觉神经元存活的外周靶标支持,并表明trkB配体对于参与心肺控制的内脏传入神经的发育可能特别重要。