Human development is breathtaking in its complexity. After an egg is fertilized by a sperm, the cell starts to divide. Some of the earliest cells in the clump are known as embryonic stem cells because they can duplicate themselves endlessly, and change themselves (or differentiate) into any cell in the body by selectively switching off some of their genes.
Later, the cells become more specialized. The neural stem cells can only differentiate into neural cells of various kinds, and skin stem cells can only differentiate into skin cells (but not neural cells), even though the underlying genes in each cell are still the same (but selectively de-activated).
As development continues, three layers of cells (germ layers) form – the “ectoderm”, “mesoderm” and “endoderm”. The mesoderm cells further develop into the muscles and blood, the endoderm develops into the digestive tract and lungs, and the ectoderm develops into the skin, nerves and brain.
It's all an iterative process of increasing cell specialization. As our hands develop, for example, they begin as tiny buds of mostly undifferentiated cells, like the hands of gingerbread men. Initially, our fingers are webbed like frog feet, but eventually the webbing cells are killed when they receive the programmed cell death signal, for which they are designed to respond.
I’m always most interested in the development of the brain itself, a process known as neurulation. The neural cells continue to differentiate into specialized neurons in the brain. A sort of chemical grid, or map, guides them as they migrate to their proper position, connecting with other neurons along the way.
There are two types of development in the early brain. Activity-independent mechanisms (such as differentiation, migration and axon guidance) proceed according to genetic programming, independent of the environment (neural activity and sensory experience).
But once the neurons are in place, with their axons connected to other neurons, activity-dependent mechanisms of development (influenced by the environment) can begin. Neurons do not connect directly with each other. Instead, there is a gap, called a synapse, between every neuron, where chemical signals pass back and forth. The chemical signals are vulnerable to being intercepted by drugs, like antidepressants and antipsychotics, because the brain is designed for exploitation by "global signals" and external agents (if not, the neurons would connect together directly).
The synaptic connections between neurons change over time, influenced by our experiences. But those are not just any experiences. They are the specific experiences for which our development was programmed to respond, like an elevator which is programmed to respond to "button presses" but not loud screams. Some genes are programmed to switch off (semi-permanently) in some people under certain environments, which is why identical twins (people with the same genes) may differ. One twin may have a slightly different experience in his life, for which a particular gene is programmed to switch off, so now the twins have, in effect, different (active) genes!
We learn skills, perfect them, and make new memories – all of which are possible by the activity of the brain. The genetically developed substructures in our brain help us remember new things (hippocampus), motivate us (amygdala), allow us to plan (frontal lobes), and learn language and other skills. Evolutionary psychologists believe we have evolved hundreds of specialized regions in the brain, each triggering specialized human desires, motivations and behaviors. Since each of us has different gene variants (probably leading to a different amygdala structure), no two people are motivated by the same things.