Medicine
New proteins help shape brain cell structures
Research suggests that these proteins play a crucial role in organizing microtubules within neurons.
Illustration: Blue Dot News
1 min read
The discovery of kinetochore proteins' role in regulating dendritic spine formation in postmitotic neurons has shed light on a complex and previously unappreciated aspect of neuronal development. Kinetochore proteins, long known for their function in cell division, have been found to play a crucial role in the proper development of hippocampal and cortical neurons.
In this study, researchers observed that kinetochore proteins were present in axons and dendrites of postmitotic iNeurons, residing at least in part at microtubule plus ends. The conditional deletion of mouse Ndc80 or Dsn1 resulted in an increase in the number of dendritic spines. Furthermore, loss of any of three kinetochore components (Ndc80, Dsn1, or Mis12) increased microtubule plus-end dynamics.
The mechanism by which kinetochore proteins regulate dendritic spine formation is multifaceted. Observations of individual microtubules in Caenorhabditis elegans indicated that Ndc80, the microtubule-binding component of the kinetochore complex, slowed the rate of microtubule growth. The increase in spine number induced by Ndc80 deletion was correlated with increased microtubule invasion of spines.
The significance of this discovery lies not only in its implications for our understanding of neuronal development but also in its connection to the fundamental processes that govern cellular behavior. As we reflect on the intricate mechanisms that underlie kinetochore proteins' role in regulating dendritic spine formation, we are reminded of the awe-inspiring complexity and beauty of the universe around us – a universe in which even the most seemingly disparate components can be revealed to be intertwined.
1 min read
In the intricate dance of neurons, a delicate balance is maintained between structure and function. Research has revealed that kinetochore proteins, long known for their role in cell division, play a crucial part in the development of hippocampal and cortical neurons. These proteins reside at the microtubule plus ends, where they help regulate the dynamics of microtubules – tiny structures that form the foundation of neuronal structure.
In postmitotic neurons, kinetochore proteins have been shown to control the formation of dendritic spines – small protrusions on the surface of neurons that receive and process signals. When these proteins are absent or impaired, the number of dendritic spines increases, leading to changes in microtubule invasion and dynamics within the spine. This delicate interplay suggests a complex mechanism by which kinetochore proteins stabilize microtubules at their plus ends.
The discovery sheds light on the intricate processes that govern neuronal development and function. It highlights the importance of understanding the role of kinetochore proteins in regulating microtubule dynamics, which is essential for maintaining proper neuronal structure and function. This research not only advances our knowledge of cellular biology but also has implications for our understanding of neurological disorders, such as those affecting cognitive function and synaptic plasticity.
1 min read
In tiny branches called axons, a key part of the brain's communication system, scientists have discovered a new role for proteins that help cells divide. These proteins, long thought to be important only during cell division, also play a crucial part in the development of brain cells after they stop dividing.
When these proteins are working properly, they help keep the tiny structures called dendritic spines from growing too big and getting in the way of the neuron's signals. But when the proteins are missing or not working right, the spines can grow too large and even more problems arise. This discovery sheds new light on how our brains develop and function, and could lead to new ways to understand and treat brain disorders.
The people behind the work
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Zhao G et al.
Author
Published in Proceedings of the National Academy of Sciences of the United States of America
Source: Proceedings of the National Academy of Sciences of the United States of America
Sources & Verification
Every statement in this story is drawn from the facts below. Each is linked to a primary or reputable source — follow any citation to check it for yourself.
- Kinetochore proteins, long studied for their role in cell division, are also required for the proper postmitotic development of hippocampal and cortical neurons. Proceedings of the National Academy of Sciences of the United States of America
- Proteins of the kinetochore complex were present in axons and dendrites of postmitotic iNeurons where they resided, at least in part, at microtubule plus ends. Proceedings of the National Academy of Sciences of the United States of America
- Conditional deletion of mouse Ndc80 or Dsn1 increased the number of dendritic spines. Proceedings of the National Academy of Sciences of the United States of America
- Loss of any of three kinetochore components (Ndc80, Dsn1, or Mis12) increased microtubule plus-end dynamics. Proceedings of the National Academy of Sciences of the United States of America
- Observations of individual microtubules in Caenorhabditis elegans indicated that Ndc80, the microtubule-binding component of the kinetochore complex, slowed the rate of microtubule growth. Proceedings of the National Academy of Sciences of the United States of America
- The increase in spine number in mammalian neurons correlated with increased microtubule invasion of spines. Proceedings of the National Academy of Sciences of the United States of America
- Both spine number and microtubule invasion phenotypes induced by Ndc80 deletion could be rescued by reexpression of Ndc80, but only if the microtubule-binding region of NDC80 was preserved. Proceedings of the National Academy of Sciences of the United States of America
- We propose that kinetochore proteins act in a complex resembling the mitotic kinetochore in order to stabilize microtubule plus ends and thereby restrain spine invasions and the development of dendritic spines. Proceedings of the National Academy of Sciences of the United States of America
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