Integrated Calendar

Most of the Pacific Northwest (PNW, USA) and British Columbia
experienced extraordinarily high air temperatures during an extreme heat
wave event (“heat dome”) in late June of 2021. In many locations, alltime
record high air temperatures (Tair) exceeding 40-45 °C were
observed. In this talk I will present evidence of the widespread impacts of
this extreme heat event. These impacts include foliar damage observed in
many locations of this region, along with some tree mortality.
Additionally, I will present data from dendrometers and eddy covariance
towers in contrasting forest types highlighting the impacts on tree growth
and ecosystem-atmosphere CO2, H2O, and energy fluxes. Better
understanding the environmental drivers, biophysical and physiological
mechanisms, and ecological consequences of heat damage incurred by
forests is of broad relevance and societal importance.

The mitoribosome translates specific mitochondrial mRNAs and regulates energy production that is a signature of all eukaryotic life forms. We present cryo-EM analyses of its assembly intermediates, mRNA binding process, and nascent polypeptide delivery to the membrane. To study the assembly mechanism, we determined a series of the small mitoribosomal subunit intermediates in complex with auxiliary factors that explain how action of step-specific factors establishes the catalytic mitoribosome. Its activation is then performed by LRPPRC that forms a stable complex with SLIRP, which delivers mRNA to the mitoribosome. In mammals, LRPPRC stabilised mRNAs co-transcriptionally, thus it links the entire gene expression system. Specific mitoribosomal proteins align the delivered mRNA with tRNA in the decoding center. This allows a nascent polypeptide to form in the tunnel, and next it needs to be delivered to the mitochondrial inner membrane. Here, we report the human mitoribosomes bound to the insertase OXA1, which elucidates the basis by which protein synthesis is coupled to membrane delivery. Finally, comparative structural and biochemical analyses reveal functionally important binding of cofactors NAD, ATP, GDP, iron-sulfur clusters and polyamines. Together with experimental identification of specific rRNA and protein modifications, the data illuminate principal components responsible for the translation of genetic material in mitochondria.

For decades, Alzheimer's disease (AD) was perceived as a disease of the neuron alone. However, research advances in recent years have challenged this concept and shed light on the critical roles of other cells within the central nervous system (CNS) and the periphery. Within the CNS, microglia and astrocytes were revealed to be key players in disease progression, while other cell types, such as oligodendrocytes, pericytes, and endothelial cells, remained relatively understudied. In my PhD, I focused on understanding how two non-neuronal cell types, the oligodendroglia in the brain parenchyma and the choroid plexus (CP) epithelium, respond to AD and how they possibly affect pathological processes. My research identified a cellular state of oligodendrocytes that significantly increased in association with brain pathology, which we termed disease-associated oligodendrocytes (DOLs). Oligodendrocytes with DOL signature could also be identified in a mouse model of tauopathy and other neurodegenerative and autoimmune inflammatory conditions, suggesting a common response of oligodendrocytes to severe deviation from homeostasis. In the second part of my PhD, I contributed to a research aiming to investigate the mechanisms underlying the decline of the CP's neuroprotective abilities in the context of AD. We found that exposure of choroid plexus epithelial cultures to 24-hydroxycholesterol (24-OH), the enzymatic product of the brain-specific enzyme cholesterol 24-hydroxylase (CYP46A1), results in downregulation of aging- related transcriptomic signatures-such as Interferon type I (IFN-I) associated inflammation. Moreover, we found that CYP46A1 is constitutively expressed by the CP of humans and mice but is reduced in AD patients and 5xFAD mice. Overexpression of Cyp46a1 at the CP in 5xFAD mice attenuated cognitive loss and brain inflammation. Our results suggest that CP CYP46A1 is an unexpected safeguard against chronic anti-viral-like responses that can be rescued when lost. Overall, my PhD work highlights the significance of studying the fate of non-neuronal cell types in neurodegenerative diseases, in general, and in AD, in particular, and emphasizes the potential of next- generation transcriptomic techniques as a powerful tool to unveil previously unexpected pathways and mechanisms involved in these diseases. 
Zoom link-https://weizmann.zoom.us/j/98815291638?pwd=cnZTanhzWkEyYmh4Mjk4OWxHMGE5UT09
Meeting ID:988 1529 1638
Password:880170

Animals distinguish sugars from non-nutritive sweeteners even in the
absence of sweet taste. This hidden sugar sense seems to reside in the gut,
but the cells and neural circuits are unknown. In 2018, the Bohórquez
Laboratory discovered a neural circuit linking the gut to the brain in one
synapse. The neural circuit is formed between neuropod cells in the gut and
the vagus nerve. This neural circuit is essential to convey sensory cues from
sugars. In 2020, the Bohórquez Laboratory discovered using a new fiber
optic technology along with optogenetics, that animals rely on neuropod cells to distinguish sugars from non-caloric sweeteners. Much like the brain
relies on retinal cone cells to see color, gut neuropod cells help the brain’s choose sugar over non-caloric sweeteners.

Herpes Simplex Virus 1 (HSV-1) is a usual suspect when it comes to Alzheimer's disease (AD), and its DNA and RNA were found in the brains and serological samples of AD patients. Such molecular presence of HSV-1 in AD is especially intriguing as HSV-1 virions are rarely detected in AD brains. To follow the molecular footsteps detected, we imaged viral proteins in postmortem human AD brains at superior resolution using expansion microscopy, a tissue manipulation method that physically expands the samples by a factor of 4.5x, allowing a 40 nm imaging resolution, and immunolabeled herpetic proteins, AD pathologies and cell markers. We found an abundance of herpetic proteins, previously undetectable with standard methods, across large brain areas. Importantly, we found that HSV-1 proteins strongly co-localized with AD pathologies. Consequently, we hypothesized that expression of HSV-1 proteins during latency may be linked to AD pathology. We are now in the process of characterizing the HSV-1 proteome in AD brains by imaging key proteins in expanded AD brain slices and examining their colocalization with AD pathologies across brain areas and disease stages. As a complementary system to the fixed human brain slices, we are exposing live human brain organoids, to HSV-1, and imaging the relationships between viral proteins and the formation of AD pathologies via expansion microscopy. Pathogens may be triggers of immune responses driving AD; this study would shed light on one common pathogen, HSV-1, while serving as a framework to unveiling molecular causation between infectious agents and AD hallmarks.