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Apoptosis in Neurodegenerative Disease, Myocardial Infarction and Cancer
Journal of Cell Science and Apoptosis
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  • Editorial   
  • J Cell Sci Apo 1:107, Vol 1(2)

Apoptosis in Neurodegenerative Disease, Myocardial Infarction and Cancer

Sarbashri Bank1*, Smarajit Maiti1 and Asru K Sinha2
1Department of Biochemistry, CMT Lab, Vidyasagar University, Midnapur-721102, India
2Department of Biochemistry, Sinha Institute of Medical Science and Technology, Kolkata, India
*Corresponding Author: Sarbashri Bank, DST Inspire SRF, Department of Biochemistry, Vidyasagar University, Midnapur, India, Tel: 91 8981719523, Email: [email protected]

Received: 30-Dec-2016 / Accepted Date: 28-Jan-2017 / Published Date: 07-Feb-2017

Editorial

Apoptosis or program cell death is a very important and normal sequential, ordered process through which cells go to death. In case of apoptosis, there is shrinkage of cell and in its nucleus, formation of blebbing, chromatin fragmentation, loss of adhesion to neighboring cells and rapid engulfment by phagocytosis. But there is contrast between apoptosis and necrosis; necrosis is caused by physical trauma or biochemical drastic changes in the cellular environment. In case of necrosis, leakage of cell contents in the medium and as a result inflammation is occurred.

In 1972, John Kerr et al. proposed the term Apoptosis in their paper where they first time described the events which occur during apoptosis.

Apoptosis is triggered by both internal stimuli such as abnormalities in the DNA and external stimuli such as cytokines [1]. From the literature, it is found that external stimuli activate apoptosis by the extrinsic signaling path way whereas internal stimuli activate intrinsic path way [2]. There is distinction between two signaling path way. Different types of internal stimuli hypoxia, irreversible DNA damage, viral infection, oxidative stress trigger apoptosis by intrinsic pathway. In this pathway, Bax and Bak help to the release of cytochrome-c from mytochondria and can complex with Apaf-1 and Procaspase-9 and trigger the apoptotic response [3]. Apaf-1 helps in the conformational changes in procaspase-9 and activates its catalytic activity. On the other hand, extrinsic signaling pathway is triggered by TNF (tumor necrosis factor), TNF binds with its receptor TNFR-1; the activated receptor then binds with TRADD, FADD and procaspase-8 through the death domain (DD) linker [4]. This multi protein complex activates the procaspase-8 and triggers to the direction of apoptosis i.e. executes to cell death.

Normal level of ordered apoptosis is very important for cell biology to maintain the homoeostasis in cellular environment. Over induced apoptosis and less activated apoptosis both are the cause of different cause of disease formation. Over induce apoptosis is the cause of neurodegenerative disorder; Alzheimer’s disease (AD) and perkinson’s disease (PD) are the neurodegenerative disorder caused by the loss of neuronal cells and as a result motor nerves loss their activity. So, the extrinsic signaling pathway (Fas ligand activation) is over activated also with the intrinsic pathway (mitochondrial degeneration; cytochrome-c, Bax and Bak over activation) [5] and triggered uncontrolled-unordered apoptosis and as a result neuronal cell loss is found.

The over-induced apoptosis is also found in myocardial infarction. Myocardial cell death is occurred by excessive apoptosis due to the low oxygen, scarcity of nutrients due to the plaque formation in coronary arteries [6]. In this hypoxic condition caspase is activated and cell death is occurred [7]. From our laboratory we reported that dermcidin isoform-2 (DCN-2), a small protein was able to activate platelet aggregation [8,9] and triggered cell death on myocardium and it was hypothesized that the event was occurred by unordered caspase activation [6]. We also explained that insulin & low dose of aspirin would inhibit the cell death trough the activation Nitric Oxide in the physiological range [6,10]. Insulin also inhibits uncontrolled cell death through the Akt pathway [10,11].

In another way, under-regulated apoptosis is the cause of cancer formation. Apoptosis is inhibited in both extrinsic and intrinsic signaling pathway. In intrinsic pathway, the expression of Bax and Bak are reduced on the other hand, the anti-apoptotic Bcl-2 family proteins (Bcl xL, Bclw) are over expressed and as a result apoptosis of tumor cell is inhibited [12]. Another tumor suppressor protein is P53 which is also reduced in presence of Bcl-2 family protein [13]. The check-points in the cell cycle do not function properly in presence of Bcl-2 and as a consequence cells are unable to control their growth. Therefore, the ratio of Bax and Bcl-2 is an important signal from that it can understand the cell will go in which direction.

So, from this short review it can be concluded that the signaling pathways of apoptosis play the pivotal role in the disease formation and its regulation. Many proteins are already discovered in these signaling pathways but there are many more proteins which are not known yet. That undiscovered protein would play the role of linker proteins which might solve or stop abnormal loss of neural cells in neurodegenerative disorders or could be able to inhibit the cancerous growth. To know the mechanism of proteins in the signaling pathways of apoptosis and antiapoptosis is one of the main aims of current science.

Acknowledgement

Sarbashri Bank, a DST Inspire SRF (DST INSPIRE Fellowship/2014/308) is thankful to Dept. of Science & Technology, Govt. of India for providing the fellowship.

References

  1. Karp G (2014) Cell and Molecular Biology Cell Signaling Pathways (7thedn) Hoboken, New Jersey John Wiley & Sons Inc.
  2. Elmore S (2007) Apoptosis a review of programmed cell death. Toxicol Pathol 35: 495-516.
  3. Wang C, Youle RJ (2009) The Role of Mitochondria in Apoptosis. Annu Rev Genet 43: 95-118.
  4. MacEwan DJ (2002) TNF ligands and receptors--a matter of life and death. Br J Pharmacol 135: 855-875.
  5. Guangwu X, Yufang S (2007) Apoptosis signaling pathways and lymphocyte homeostasis. Cell Research 17: 759-771.
  6. Bank S, Maiti S, Guha S, Sinha AK (2016) TRIAD system catalase, insulin, and low dose aspirin neutralize the effect of dermcidin isoform-2 and prevent cell death in acute myocardial infarction and recurrence of the disease. Cardiol J 23: 623-625.
  7. Greijer AE, Vander WE (2004) The role of hypoxia inducible factor 1 (HIF-1) in hypoxia induced apoptosis. J Clin Pathol 57: 1009-1014.
  8. Bank S, Jana P, Maiti S, Guha S, Sinha AK (2014) Dermcidin isoform-2 induced nullification of the effect of acetyl salicylic acid in platelet aggregation in acute myocardial infarction. Sci Rep 4: 5804.
  9. Ghosh R (2011) The appearance of dermcidin isoform 2, a novel platelet aggregating agent in the circulation in acute myocardial infarction that inhibits insulin synthesis and the restoration by acetyl salicylic acid of its effects. J Thromb Thrombolysis 31: 13-21.
  10. Mannick JB, Miao XQ, Stamler JS (1997) Nitric oxide inhibits Fas-induced apoptosis. J Biol Chem 272: 24125-24128.
  11. Si R, Tao L, Zhang HF, Yu QJ, Zhang R, et al. (2011) Survivin a novel player in insulin cardioprotection against myocardial ischemia/reperfusion injury. Journal of molecular and cellular cardiology 50: 16-24.
  12. Yip KW, Reed JC (2008) Bcl-2 family proteins and cancer. Oncogene 27: 6398-6406.
  13. Beham A (1997) Bcl-2 inhibits p53 nuclear import following DNA damage. Oncogene 15: 2767-2772.

Citation: Bank S, Maiti S, Sinha AK (2017) Apoptosis in Neurodegenerative Disease, Myocardial Infarction and in Cancer. J Cell Sci Apo 1: 107.

Copyright: ©2017 Bank S, et al. 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.

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