Knight Cardiovascular Institute; Oregon Health & Science University; Portland, OR USA.
Organogenesis. 2013 Jul-Sep;9(3):176-93. doi: 10.4161/org.24892. Epub 2013 May 14.
Autonomic cardiac neurons have a common origin in the neural crest but undergo distinct developmental differentiation as they mature toward their adult phenotype. Progenitor cells respond to repulsive cues during migration, followed by differentiation cues from paracrine sources that promote neurochemistry and differentiation. When autonomic axons start to innervate cardiac tissue, neurotrophic factors from vascular tissue are essential for maintenance of neurons before they reach their targets, upon which target-derived trophic factors take over final maturation, synaptic strength and postnatal survival. Although target-derived neurotrophins have a central role to play in development, alternative sources of neurotrophins may also modulate innervation. Both developing and adult sympathetic neurons express proNGF, and adult parasympathetic cardiac ganglion neurons also synthesize and release NGF. The physiological function of these "non-classical" cardiac sources of neurotrophins remains to be determined, especially in relation to autocrine/paracrine sustenance during development. Cardiac autonomic nerves are closely spatially associated in cardiac plexuses, ganglia and pacemaker regions and so are sensitive to release of neurotransmitter, neuropeptides and trophic factors from adjacent nerves. As such, in many cardiac pathologies, it is an imbalance within the two arms of the autonomic system that is critical for disease progression. Although this crosstalk between sympathetic and parasympathetic nerves has been well established for adult nerves, it is unclear whether a degree of paracrine regulation occurs across the autonomic limbs during development. Aberrant nerve remodeling is a common occurrence in many adult cardiovascular pathologies, and the mechanisms regulating outgrowth or denervation are disparate. However, autonomic neurons display considerable plasticity in this regard with neurotrophins and inflammatory cytokines having a central regulatory function, including in possible neurotransmitter changes. Certainly, neurotrophins and cytokines regulate transcriptional factors in adult autonomic neurons that have vital differentiation roles in development. Particularly for parasympathetic cardiac ganglion neurons, additional examinations of developmental regulatory mechanisms will potentially aid in understanding attenuated parasympathetic function in a number of conditions, including heart failure.
自主心脏神经元具有神经嵴的共同起源,但在向成年表型成熟的过程中经历了明显的发育分化。祖细胞在迁移过程中对排斥信号做出反应,然后来自旁分泌源的分化信号促进神经化学和分化。当自主轴突开始支配心脏组织时,血管组织中的神经营养因子对于神经元在到达靶标之前的维持是必不可少的,之后靶标衍生的营养因子接管最终成熟、突触强度和出生后存活。尽管靶标衍生的神经营养因子在发育中起着核心作用,但替代的神经营养因子来源也可能调节神经支配。发育中和成年的交感神经元都表达 proNGF,而成年副交感心脏神经节神经元也合成和释放 NGF。这些“非经典”心脏神经营养素来源的生理功能仍有待确定,特别是在发育过程中与自分泌/旁分泌维持有关。心脏自主神经在心脏丛、神经节和起搏区密切空间相关,因此对来自相邻神经的神经递质、神经肽和营养因子的释放敏感。因此,在许多心脏病理中,自主神经系统的两个分支之间的失衡对于疾病进展至关重要。尽管交感和副交感神经之间的这种串扰在成年神经中已经得到很好的证实,但在发育过程中,自主神经支之间是否存在一定程度的旁分泌调节尚不清楚。异常神经重塑是许多成年心血管病理中的常见现象,调节生长或去神经支配的机制也不同。然而,自主神经元在这方面表现出相当大的可塑性,神经营养因子和炎症细胞因子具有中央调节作用,包括可能的神经递质变化。当然,神经营养因子和细胞因子调节成年自主神经元中的转录因子,这些转录因子在发育中具有重要的分化作用。特别是对于副交感心脏神经节神经元,对发育调节机制的进一步研究可能有助于理解许多情况下副交感功能减弱的情况,包括心力衰竭。