Heterozygous knockout of Synaptotagmin13 phenocopies ALS features and TP53 activation in human motor neurons.

Spinal motor neurons (MNs) represent a highly vulnerable cellular population, which is affected in fatal neurodegenerative diseases such as amyotrophic lateral sclerosis (ALS) and spinal muscular atrophy (SMA). In this study, we show that the heterozygous loss of SYT13 is sufficient to trigger a neurodegenerative phenotype resembling those observed in ALS and SMA. SYT13+/- hiPSC-derived MNs displayed a progressive manifestation of typical neurodegenerative hallmarks such as loss of synaptic contacts and accumulation of aberrant aggregates. Moreover, analysis of the SYT13+/- transcriptome revealed a significant impairment in biological mechanisms involved in motoneuron specification and spinal cord differentiation. This transcriptional portrait also strikingly correlated with ALS signatures, displaying a significant convergence toward the expression of pro-apoptotic and pro-inflammatory genes, which are controlled by the transcription factor TP53. Our data show for the first time that the heterozygous loss of a single member of the synaptotagmin family, SYT13, is sufficient to trigger a series of abnormal alterations leading to MN sufferance, thus revealing novel insights into the selective vulnerability of this cell population.

Synaptogenic gene therapy with FGF22 improves circuit plasticity and functional recovery following spinal cord injury.

Functional recovery following incomplete spinal cord injury (SCI) depends on the rewiring of motor circuits during which supraspinal connections form new contacts onto spinal relay neurons. We have recently identified a critical role of the presynaptic organizer FGF22 for the formation of new synapses in the remodeling spinal cord. Here, we now explore whether and how targeted overexpression of FGF22 can be used to mitigate the severe functional consequences of SCI. By targeting FGF22 expression to either long propriospinal neurons, excitatory interneurons, or a broader population of interneurons, we establish that FGF22 can enhance neuronal rewiring both in a circuit-specific and comprehensive way. We can further demonstrate that the latter approach can restore functional recovery when applied either on the day of the lesion or within 24 h. Our study thus establishes viral gene transfer of FGF22 as a new synaptogenic treatment for SCI and defines a critical therapeutic window for its application.

Accelerating upward treeline shift in the Altai Mountains under last-century climate change.

Treeline shift and tree growth often respond to climatic changes and it is critical to identify and quantify their dynamics. Some regions are particularly sensitive to climate change and the Altai Mountains, located in Central and East Asia, are showing unequivocal signs. The mean annual temperature in the area has increased by 1.3-1.7 °C in the last century. As this mountain range has ancient and protected forests on alpine slopes, we focus on determining the treeline structure and dynamics. We integrated in situ fine-scale allometric data with analyses from dendrochronological samples, high-resolution 3D drone photos and new satellite images to study the dynamics and underlying causal mechanisms of any treeline movement and growth changes in a remote preserved forest at the Aktru Research Station in the Altai Mountain. We show that temperature increase has a negative effect on mountain tree growth. In contrast, only younger trees grow at higher altitudes and we document a relatively fast upward shift of the treeline. During the last 52 years, treeline moved about 150 m upward and the rate of movement accelerated until recently. Before the 1950s, it never shifted over 2150-2200 m a.s.l. We suggest that a continuous upward expansion of the treeline would be at the expense of meadow and shrub species and radically change this high-mountain ecosystem with its endemic flora. This documented treeline shift represents clear evidence of the increased velocity of climate change during the last century.