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From the Outset, We Spread Rapidly

The original cell, resembling a single hair shaft, gave rise to the ten trillion cells that constitute each individual body. While we are not merely bags of identical cells, the development process leads to around two hundred distinct cell types. We are enclosed by these diverse cell structures.

Initially Infectious: From the Outset
Initially Infectious: From the Outset

From the Outset, We Spread Rapidly

In the realm of biology, viruses are often seen as harmful agents, but a closer look reveals that they can also play a crucial role in the development of living organisms. This is particularly true for endogenous retroviruses, as demonstrated in various studies and research.

One such example is HIV, a virus that inserts its genes into the DNA of a cell, making a living this way. However, the focus of recent research has shifted towards endogenous retroviruses that have integrated into the DNA of cells, becoming a permanent part of the body.

Scientists have discovered that during the earliest stage of embryo development, virus-controlled genes are active. These genes are crucial for making cells totipotent, meaning they can give rise to any part of the embryo, as well as the placenta and other tissue outside the embryo. This 'magic state' of cells holds immense potential for regenerative medicine.

Researchers, such as Marisa Bartolomei and others in the field of developmental biology and virology, have been studying endogenous retroviruses and their regulatory elements. Their work has enabled the domestication of these viral promoters in the early stages of mammalian embryo development.

This discovery could lead to a 'delicious triumph' in regenerative medicine. Scientists are currently reprogramming cells to goose them back into an early state for potential treatments for Parkinson's disease and other disorders. The idea is to switch on these virus-controlled genes to help push cells back to a magic state.

One practical application of this hypothesis is proposed by Pfaff and his colleagues, who suggest that the domestication of these virus promoters was a key step in the evolution of mammals with placentas.

In a study, over 100 genes were found to be active in human egg cells during the two-cell stage, which then shut down later in development. This suggests that once genes are silenced, totipotent cells become pluripotent, capable of forming any cell type in the body, but not the extraembryonic tissues like the placenta.

However, the application of this research is not without its challenges. For instance, koalas are currently suffering from an epidemic of one such endogenous retrovirus. The book 'A Planet of Viruses' discusses these inner passengers in more detail, providing a comprehensive look at the role of viruses in our bodies.

It is important to note that a human body contains approximately 10 trillion cells, and human development involves the production of a couple hundred types of cells. The human genome contains about 100,000 fragments of endogenous retroviruses, making up about 8% of all DNA. This underscores the significant role that viruses, particularly retroviruses, play in human development.

As research continues, the potential applications of endogenous retroviruses in regenerative medicine are becoming increasingly clear. The future of medicine may very well be shaped by our understanding and harnessing of these inner passengers.

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