Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.

Saturday, June 24, 2023

Insight into protein synthesis in axon regeneration

How is your doctor using this to successfully reconnect neurons for your recovery? 

Your doctor should have intuited that this could work for stroke rehab way back in September 2015. If not you don't have a functioning stroke doctor.

Protein synthesis in regenerating spinal cord axons September 2015 

The latest here:

Insight into protein synthesis in axon regeneration

Abstract

Successful axon regeneration is crucial for the treatment of numerous nerve injuries and neurodegenerative diseases, which requires adequate and accurate protein synthesis, including mRNA translation, both in the neuron somas and locally in the axons. Recent studies have shed light on novel functions and mechanisms of protein synthesis that are relevant for axon regeneration, with a particular focus on local translation. Here, we review the new developed technologies and approaches for investigating local translation, discuss the roles of local translation in axon regeneration, and summarize the key signaling molecules and pathways that regulate local translation during axon regeneration. Additionally, we give an overview of local translation in the peripheral and central nervous systems neurons and the latest progress in protein synthesis in neuron somas respectively. Finally, we consider the potential directions for future research in this field to provide insights into protein synthesis in axon regeneration.

Introduction

Numerous disorders involving axon damage can benefit from successful axon regeneration, including stroke, traumatic brain injury, spinal cord injury, peripheral nerve injury, and a range of neurodegenerative diseases (Li et al., 2020; Qian and Zhou, 2020). As a complex and synergistic process involving multiple cellular events, axon regeneration requires the sustained activity of structural and regulatory proteins in both neuronal somas and axons (Rozenbaum et al., 2018; Terenzio et al., 2018; Zheng et al., 2001), implying that de novo protein synthesis in somas and axons is critical for axon regeneration in adult mammalian nervous systems (Belin et al., 2015; Donnelly et al., 2013; Weng et al., 2018). Due to technical constraints, it has long been believed that transcripts and their translational machinery are found in the dendrites of neurons but not in axons. Although polysomes have been found at the base of dendritic spines (Steward and Levy, 1982), mature axons typically exhibit low levels of ribosomes, which are primarily localized in periaxoplasmic ribosomal plaques (Calliari et al., 2014; Koenig et al., 2000; Sotelo-Silveira et al., 2008; Sotelo-Silveira et al., 2004). Thus, the prevalent view has been that axons are incapable of locally synthesizing proteins.

However, with methodological advances, it was eventually discovered that axon compartments contain a variety of RNA molecules, including ribosomal RNA, transfer RNA, and messenger RNA (Koenig, 1979; Koenig et al., 2000; Van Minnen, 1994; Weiner et al., 1996), suggesting protein synthesis in axons. The earliest direct evidence of local translation in mature mammalian axons came from sensory neurons in the peripheral nervous system (PNS). Zhang et al. separated pure regenerating axons from the dorsal root ganglion (DRG) cell bodies, and found that the axons can actively synthesize proteins (Zheng et al., 2001). Then numerous studies demonstrated that mature neurons in the central nervous system (CNS) can also synthesize proteins in their axons (Baleriola et al., 2014; Kalinski et al., 2015). And the local protein synthesis dynamically control the neuronal function in the CNS (Akins et al., 2017; Monday et al., 2022). In addition, studies have revealed that translation and ribosome biogenesis are rate-limiting processes for axon and dendrite growth (Slomnicki et al., 2016; Williams et al., 2016) and that the equilibrium of protein synthesis in the soma and axon influences axonal growth rates (Perry et al., 2016). These observations suggest that protein synthesis regulation at the levels of both axons and somas plays an important role in axon regeneration.

However, compared with transcriptional regulation, translational regulation in axon repair after injury is less understood. This emerging field is working toward the goal of revealing novel functions of protein synthesis in axon regeneration and identifying potential pharmacological targets in nerve injury or neurodegenerative diseases. Here, we will discuss these functions and provide a brief overview of the current understanding of the underlying mechanisms, including local translation and protein synthesis in the soma. Furthermore, we discuss what advancements in this field can be expected in the future.

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