Issue 4, 2005

By the abstracts:

"Two Hands Make Light Work of Gene Modification". About a then new DNA-modification technique where they combined zinc-fingers and nucleases to chop the DNA wherever they wanted. The idea is to put a suitable replacement patch into the cell, and letting the cell's repair system patch the substitute in. A very similar idea has been making the rounds lately and has been advertised as an easier and cheaper version of the one used in this paper.

"Mitochondrial DNA Mutations, Apoptosis, and the Misfolded Protein Response" seems to be a theoretical paper postulating a mechanism explaining the results of experiments in mice with mutant mitochondrial DNA polymerase. They claim that the main way that mitochondrial mutations drive aging is that mutated proteins occasionally trigger apoptosis by interacting with mitochondrial membrane proteins. This then triggers compensatory effects of the tissue to this loss of cells. In the abstract they mention that heart tissue upregulates anti-apoptotic signals and also drives the rest of the surviving heart cells hard to compensate for pumping loss. In this model, ROS triggers the mtDNA mutations but is not a major part of the downstream mechanism (sort of the reverse of http://readingrejuvenationresearch.blogspot.com.au/2013/03/mitochondrial-microheteroplasmy-and.html, although very obviously related).  I found a summary that looks to be an extract from the paper at http://crabsallover.blogspot.com.au/2006/11/mitochondrial-dna-mutations-apoptosis.html. I'll read the rest if I find it.

"Cellular Responses to Protein Accumulation Involve Autophagy and Lysosomal Enzyme Activation". Study of what happens when high level of protein gunk builds up on neurons in vitro. Lysosomes and macroautophagy are activated, but not enough to compensate.

"A Yang-Invigorating Chinese Herbal Formula Enhances Mitochondrial Functional Ability and Antioxidant Capacity in Various Tissues of Male and Female Rats". Chinese herbal formula upregulates SODs in rats.

"NANOG Changes in Mouse Kidneys with Age". Tracking of expression of NANOG, gene needed to keep pluripotency and one of the genes introduced to create iPSCs later, in mice's kidneys as they age. Expression goes down.

Also, there was a report on the 11th Congress of the International Association of Biomedical Gerontology which I'd like to read.