Minerva Foundation Institute for Medical Research, Tukholmankatu 8, 00290 Helsinki, Finland.
HiLIFE-Neuroscience Center, University of Helsinki, 00014 Helsinki, Finland.
Cells. 2021 Sep 12;10(9):2392. doi: 10.3390/cells10092392.
Dendritic spines are small, bulbous protrusions along neuronal dendrites where most of the excitatory synapses are located. Dendritic spine density in normal human brain increases rapidly before and after birth achieving the highest density around 2-8 years. Density decreases during adolescence, reaching a stable level in adulthood. The changes in dendritic spines are considered structural correlates for synaptic plasticity as well as the basis of experience-dependent remodeling of neuronal circuits. Alterations in spine density correspond to aberrant brain function observed in various neurodevelopmental and neuropsychiatric disorders. Dendritic spine initiation affects spine density. In this review, we discuss the importance of spine initiation in brain development, learning, and potential complications resulting from altered spine initiation in neurological diseases. Current literature shows that two Bin Amphiphysin Rvs (BAR) domain-containing proteins, MIM/Mtss1 and SrGAP3, are involved in spine initiation. We review existing literature and open databases to discuss whether other BAR-domain proteins could also take part in spine initiation. Finally, we discuss the potential molecular mechanisms on how BAR-domain proteins could regulate spine initiation.
树突棘是神经元树突上的小球状突起,大多数兴奋性突触都位于此处。正常人类大脑中的树突棘密度在出生前后迅速增加,在 2-8 岁时达到最高密度。在青春期期间密度会下降,在成年期达到稳定水平。树突棘的变化被认为是突触可塑性的结构相关物,也是神经元回路依赖经验重塑的基础。树突棘密度的改变与各种神经发育和神经精神疾病中观察到的异常大脑功能相对应。树突棘的起始会影响树突棘密度。在这篇综述中,我们讨论了树突棘起始在大脑发育、学习中的重要性,以及神经疾病中树突棘起始改变所导致的潜在并发症。目前的文献表明,两种含有 Bin 结构域的 Amphiphysin Rvs(BAR)结构域蛋白 MIM/Mtss1 和 SrGAP3 参与了树突棘的起始。我们综述了现有文献和开放数据库,以讨论其他 BAR 结构域蛋白是否也可以参与树突棘的起始。最后,我们讨论了 BAR 结构域蛋白如何调节树突棘起始的潜在分子机制。