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Nucleus and Cytoplasm Macromolecular Communication
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Journal of Cytology & Histology

ISSN: 2157-7099

Open Access

Mini Review - (2023) Volume 14, Issue 4

Nucleus and Cytoplasm Macromolecular Communication

Gianrico Leuci*
*Correspondence: Gianrico Leuci, Department of Pathology, Stanford University, CA 94304, USA, Email:
Department of Pathology, Stanford University, CA 94304, USA

Received: 01-Jul-2023, Manuscript No. jch-23-111086; Editor assigned: 03-Jul-2023, Pre QC No. P-111086; Reviewed: 15-Jul-2023, QC No. Q-111086; Revised: 20-Jul-2023, Manuscript No. R-111086; Published: 27-Jul-2023 , DOI: 10.37421/2157-7099.2023.14.693
Citation: Leuci, Gianrico. “Nucleus and Cytoplasm Macromolecular Communication.” J Cytol Histol 14 (2023): 693.
Copyright: © 2023 Leuci G. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

The cytoplasm, a vital component of cells, plays a crucial role in various cellular processes. It is a complex and dynamic region filled with a diverse array of structures and molecules. In this article, we will delve into the fascinating world of cytoplasmic features and explore their functions within the cell. One of the prominent features of the cytoplasm is the cytosol, a gel-like substance that fills the space between the cell membrane and the nucleus. The cytosol is composed of water, ions, small molecules, and proteins, and serves as a medium for cellular metabolism. It facilitates the movement of molecules within the cell, allowing for chemical reactions and signaling processes to occur. Within the cytoplasm, various organelles are suspended, each with distinct roles and functions. One of the most well-known organelles is the mitochondrion, often referred to as the "powerhouse of the cell." Mitochondria are responsible for generating Adenosine Triphosphate (ATP), the energy currency of the cell, through a process known as oxidative phosphorylation. Additionally, mitochondria are involved in calcium storage, cell signaling, and apoptosis, highlighting their multifaceted nature.

Keywords

Nucleus • Cytoplasm • Macromolecular • Phosphorylation

Introduction

Another significant cytoplasmic organelle is the Endoplasmic Reticulum (ER), a network of interconnected membrane-bound tubules and sacs. The ER can be further divided into two regions: the Rough Endoplasmic Reticulum (RER) and the Smooth Endoplasmic Reticulum (SER). The RER is studded with ribosomes and is primarily responsible for protein synthesis and processing. The SER, on the other hand, lacks ribosomes and participates in lipid metabolism, detoxification reactions, and the storage and release of calcium ions. Moving on, we encounter the Golgi apparatus, often likened to a cellular post office. It consists of a series of stacked membrane-bound compartments called cisternae. The Golgi apparatus receives proteins and lipids from the ER, modifies them, and packages them into vesicles for transport to their final destinations. It plays a pivotal role in protein sorting, glycosylation, and the formation of lysosomes and secretory vesicles.

Lysosomes are membrane-bound organelles filled with digestive enzymes. They are responsible for the degradation of cellular waste, damaged organelles, and engulfed pathogens through a process called autophagy. Lysosomes maintain cellular homeostasis by recycling macromolecules and providing the cell with essential building blocks. In addition to organelles, the cytoplasm also contains a network of protein filaments known as the cytoskeleton. The cytoskeleton is composed of three main components: microfilaments, intermediate filaments, and microtubules. Microfilaments, consisting of the protein actin, provide structural support and facilitate cellular movement. Intermediate filaments provide mechanical strength and stability to the cell, while microtubules, made up of tubulin, are involved in intracellular transport, cell division, and the maintenance of cell shape [1].

Literature Review

Furthermore, the cytoplasm harbors numerous membrane-less organelles called biomolecular condensates. These condensates are formed through phase separation, a process in which molecules segregate from the cytoplasm to form distinct liquid-like compartments. Biomolecular condensates play critical roles in cellular processes such as gene expression, RNA processing, and signaling, acting as hubs for specific molecular interactions. Additionally, the cytoplasmic features described above are not static entities but rather exhibit dynamic properties that allow for intricate cellular processes to occur. For instance, organelles such as mitochondria, endoplasmic reticulum, and Golgi apparatus undergo continuous movement and rearrangement within the cytoplasm. This mobility enables efficient communication and coordination between different organelles, ensuring the smooth flow of materials and information throughout the cell.

Discussion

The cytoplasmic features also interact with each other in a highly coordinated manner. For example, the endoplasmic reticulum and mitochondria form close associations known as mitochondria-associated ER Membranes (MAMs). These specialized contact sites facilitate the exchange of lipids, calcium ions, and signaling molecules between the two organelles, thereby influencing various cellular processes such as energy metabolism, calcium homeostasis, and apoptosis. Furthermore, the cytoplasmic features actively participate in cellular signaling and response mechanisms. Signaling molecules, such as hormones or growth factors, can trigger a cascade of events within the cytoplasm, leading to specific cellular responses. These signals are often transmitted through the cytoplasmic network, utilizing the cytoskeleton as a highway for molecular transport and directing the movement of organelles and vesicles to specific cellular locations [2].

The cytoplasmic features are also intricately involved in cell division. During mitosis, the microtubules of the cytoskeleton form the mitotic spindle, a structure essential for the proper segregation of chromosomes into daughter cells. Additionally, the endoplasmic reticulum and Golgi apparatus play crucial roles in organizing and distributing cellular components necessary for the formation of new cells. Moreover, the cytoplasmic features can undergo alterations and adaptations in response to cellular conditions or external stimuli. For instance, stress conditions can trigger the formation of stress granules, which are cytoplasmic aggregates composed of RNA and proteins. These granules serve as temporary storage sites for cellular components during stress, allowing the cell to re-establish homeostasis once the stressor is removed [3,4].

In recent years, there has been increasing interest in the study of biomolecular condensates, as they have been implicated in various cellular processes and disease states. These condensates, formed through liquidliquid phase separation, can concentrate specific molecules and facilitate their interactions, leading to the formation of membrane less compartments with unique properties. Research on biomolecular condensates has provided insights into the regulation of gene expression, RNA processing, and the formation of membrane less organelles, highlighting the importance of cytoplasmic features beyond traditional membrane-bound organelles [5,6].

Conclusion

In conclusion, the cytoplasmic features within cells are not only diverse and complex but also highly interconnected and dynamic. They play essential roles in cellular metabolism, communication, transport, signaling, division, and adaptation. Understanding the functions and interactions of these cytoplasmic features is crucial for unraveling the complexities of cellular biology and advancing our knowledge of fundamental biological processes. Continued research in this field holds great promise for shedding light on human health, disease mechanisms, and potential therapeutic targets. The cytoplasm is a dynamic and intricate environment within the cell, hosting a wide array of structures and molecules. From organelles like mitochondria, endoplasmic reticulum, Golgi apparatus, and lysosomes, to the cytoskeleton, biomolecular condensates, and transport vesicles, each cytoplasmic feature contributes to the overall functionality and survival of the cell. Understanding these cytoplasmic features and their interactions provides valuable insights into cellular processes and is crucial for advancing our knowledge of cell biology and human health.

Acknowledgement

None.

Conflict of Interest

There are no conflicts of interest by author.

References

  1. Hudemann, Christoph, Yvonne Exner, Robert Pollmann and Karina Schneider, et al. "IgG against the membrane-proximal portion of the desmoglein 3 ectodomain induces loss of keratinocyte adhesion, a hallmark in pemphigus vulgaris." J Invest Dermatol 143 (2023): 254-263.
  2. Google Scholar, Crossref, Indexed at

  3. Schauer, Franziska, Norito Ishii, Maja Mockenhaupt and Leena Bruckner-Tuderman, et al. "Radiation-associated pemphigus vulgaris in a patient with preceding malignancy: Treatment with rituximab as a valuable option." Front immunol 10 (2020): 3116.
  4. Google Scholar, Crossref, Indexed at

  5. Saha, M., B. Bhogal, M. M. Black and D. Cooper, et al. "Prognostic factors in pemphigus vulgaris and pemphigus foliaceus." Br J Dermatol 170 (2014): 116-122.
  6. Google Scholar, Crossref, Indexed at

  7. He, Wenxiu, Yixiao Xing, Chunlei Li and Peiru Zhou, et al. "Identification of Six MicroRNAs as potential biomarkers for pemphigus vulgaris: From diagnosis to pathogenesis." Diagn 12 (2022): 3058.
  8. Google Scholar, Crossref, Indexed at

  9. Culton, Donna A., Suzanne K. McCray, Moonhee Park and James C. Roberts, et al. "Mucosal pemphigus vulgaris anti-Dsg3 IgG is pathogenic to the oral mucosa of humanized Dsg3 mice." J Invest Dermatol 135 (2015): 1590-1597.
  10. Google Scholar, Crossref, Indexed at

  11. Lotti, Roberta, Claudio Giacinto Atene, Emma Dorotea Zanfi and Matteo Bertesi, et al. "In vitro, ex vivo, and in vivo models for the study of pemphigus." Int J Mol Sci 23 (2022): 7044.
  12. Google Scholar, Crossref, Indexed at

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