We talked about the importance of the circadian rhythm in proper organismal function and health, and tooth development and dental health is not to be overlooked. A research group from Wuhan University in China was curious as to how the circadian rhythm would affect the regulation of ameloblast differentiation. 1 The ameloblast is a specialized cell that is key to the development of enamel, the hardest tissue in the human body that strengthens teeth and allows us to eat a variety of foods. Enamel does not have much regenerative ability, and therefore must last our entire lives, so the proper differentiation and function of ameloblasts is critical to dental health. The authors of this study built off previous findings that both circadian genes and markers of ameloblast differentiation would oscillate. They used circadian disruption techniques in mice to show that knocking down the period gene PER2 would lead to decreased expression of critical gene products and inhibit enamel formation. While this finding is quite niche, it gives us yet another reason to be thankful for an orderly circadian rhythm!
Recently, a Massachusetts-based biotechnology company showed that small molecule therapy could be used to reprogram progenitor cells in the inner ear to reproduce the hair cells that could potentially reverse hearing loss in deaf patients. Researchers from Shandong University in China noted that annexin A4 (ANXA4) is expressed in hair cells, but wanted to understand its function in the development and function of those cells. 2 The unexpected result was that ANXA4 knockout did not affect hair cell function at all, suggesting that other annexins might serve a redundant function. While this would sometimes be considered a “negative result,” this will provide other avenues to explore the function of ANXA4 in these particular cells.
Here are the ABclonal antibody products (with catalog numbers) used in this study:
Here are the ABclonal antibody products (with catalog numbers) used in this study:
In the context of traumatic brain injury, scientists from Huazhong University in China studied the effects of an anti-inflammatory drug, BAY61-3606, in modulating microglial cells (the immune cells in the nervous system) and damage to neurons. 5 Treatment with BAY61-3606 was able to reduce inflammation in both cell and mouse models of brain injury. This finding is encouraging as a possible treatment strategy for people who have suffered brain injury due to accidents, and also professional athletes suffering from concussions such as American football and ice hockey players.
In all cells of all organisms, dehydrogenase and reductase enzymes are required for most life functions including the processing of metabolites and macromolecules. Much is still unknown about the human microsomal dehydrogenase reductase 9 (DHRS9), including its target substrates. A collaboration between American universities sought to determine this substrate preference. 6 The study found that DHRS9 reacted against oxylipins, which are lipids generated by oxidation, and are implicated in the inflammatory response. This discovery may contribute to further mechanistic studies of DHRS9 in disease progression associated with inflammation.
Macrophages are critical to the immune response from the time of embryo implantation into the uterus. Unfortunately, sometimes tumors are able to seize macrophages into their microenvironment and use inflammatory response for their own gains. In a collaboration between Chinese and American universities, scientists studying the role of macrophages during early pregnancy were able to show that blocking lactic acid uptake by macrophages could prevent pregnancy loss. 7 The study involved targets in lactic acid metabolism (LDHA), hypoxia (HIF-2alpha), and signal transduction pathways (SRC), among many others (what a lovely customer!). While the study was performed in the context of a pregnancy model, knowing that lactic acid also plays a role in tumorigenesis, this finding may suggest a new method to temper tumor progression.
Here are the ABclonal antibody products (with catalog numbers) used in this study:
Prostate cancer remains one of the leading causes of death in men. A group from Stanford University presented a small molecule termed SU086 as a therapy against advanced prostate cancer. 9 The molecule targets heat shock protein 90 (HSP90), impairs glycolysis, and reduces prostate tumor growth, migration, and invasion in cell lines and tissues derived from patients. The apparently low toxicity of SU086 in mice suggests it may be an effective therapy for prostate cancer once cleared for human clinical trials.
Here are the ABclonal antibody products (with catalog numbers) used in this study:
Messenger RNA has a fleeting lifespan, with highly regulated checkpoints from the initiation of transcription all the way through to degradation. Scientists from the University of Victoria in Canada were interested in further defining the particulars of ARS2-mediated RNA metabolism. 10 They showed that ARS can be alternative spliced into two distinct isoforms, one that operates in the cytoplasm, with the other isoform remaining in the nucleus. Switching between ARS isoforms has implications in proper RNA turnover and the ability of the cell to sense stress stimuli, including toxins such as arsenic.
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