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International Research Journals

Perspective - International Research Journal of Basic and Clinical Studies ( 2023) Volume 8, Issue 2

Phenotypic Variety and Possible Therapeutic Uses of Peripheral Blood Stem Cells

Pawan Mishra*
 
Department of Clinical Nutrition and Dietetics, University Clinical Research, Indonesia
 
*Corresponding Author:
Pawan Mishra, Department of Clinical Nutrition and Dietetics, University Clinical Research, Indonesia, Email: PawaMishra54@gmail.com

Received: 01-Apr-2023, Manuscript No. irjbcs-23-96380; Editor assigned: 03-Apr-2023, Pre QC No. irjbcs-23-96380 (PQ); Reviewed: 17-Apr-2023, QC No. irjbcs-23-96380; Revised: 20-Apr-2023, Manuscript No. irjbcs-23-96380 (R); Published: 28-Apr-2023, DOI: 10.14303/irjbcs.2023.33

Abstract

Peripheral blood contains a tiny percentage of pluripotent stem cells. It is believed that these peripheral blood stem cells (PBSCs) are diverse and have a wide range of clinical uses. Unknown is the precise number of separate populations. Individual PBSC populations that have been identified by various experimental approaches probably share or overlap, while having different designations. Hematopoietic stem cells (HSCs), CD34- stem cells, CD14+ stem cells, mesenchymal stem cells (MSCs), very small embryonic-like (VSEL) stem cells, endothelial progenitor cells (EPCs), and other pluripotent stem cells are the seven categories into which we have divided PBSCs in this quick study. We go through the main traits of these stem/progenitor cell groups as well as some of their potential uses in ophthalmology.

Keywords

Growth media, Tissue banks, Tissue transplantation

INTRODUCTION

Umbilical cord blood (UCB) contains both stem cells and progenitor cells in significant quantities; making these cells an important target population for both experimental and clinical studies (Sayed YF., et al 2019). The idea of UCB banking for future use has gained popularity since the utilisation of autologous or allogeneic hematopoietic stem cell transplantation in the treatment of various diseases has expanded quickly in recent years (Aljabali AA., et al 2020). Compared to adult stem cells, UCB stem and progenitor cells have a number of advantages, including their immaturity (which may significantly lower rejection upon transplantation into a mismatched host) and capacity to create huge amounts of homogenous tissue or cells (Oun AA., et al 2020). These cells can also develop into brain, cardiac, epithelial, hepatic, and dermal tissues crossing tissue lineage barriers. A other cell source that is ethically ok and has a lot of public acceptance is human UCB (Yaqoob AA., et al 2020). The features of human UCB-derived stem and progenitor cells are outlined in this research along with their potential therapeutic applications for tissue and cell regeneration (Ni Q., et al 2020). All stem cell biologists can benefit from the conceptual, experimental, and therapeutic approaches developed via the study of haematopoiesis, the lifelong process of blood cell line formation (Renu S., et al 2020). From a therapeutic standpoint, no other use of stem cell biology has proved as successful as bone marrow and cord blood transplantation for the treatment of blood disorders (Collins KA., et al. 2017). The study of stem cells from embryonic, foetal, and different adult tissues has recently become a focus of stem cell biology research, opening up new perspectives on the identification, origin, and full therapeutic potential of tissue-specific stem cells (Xiang SD., et al. 2018).

DISCUSSION

Umbilical cord blood (UCB) contains both stem cells and progenitor cells in significant quantities, making these cells an important target population for both experimental and clinical studies (Ding P., et al 2019). The idea of UCB banking for future use has gained popularity since the utilisation of autologous or allogeneic hematopoietic stem cell transplantation in the treatment of various diseases has expanded quickly in recent years. Compared to adult stem cells, UCB stem and progenitor cells have a number of advantages, including their immaturity (which may significantly lower rejection upon transplantation into a mismatched host) and capacity to create huge amounts of homogenous tissue or cells. These cells can also develop into brain, cardiac, epithelial, hepatic, and dermal tissues crossing tissue lineage barriers (Zhu G., et al 2017). A other cell source that is ethically ok and has a lot of public acceptance is human UCB. The features of human UCBderived stem and progenitor cells are outlined in this research along with their potential therapeutic applications for tissue and cell regeneration.

CONCLUSION

Despite accumulating evidence that mesenchymal stem cells (MSCs) are present in a variety of illnesses, the majority of therapeutic applications have centred on MSCs derived from adult bone marrow, making them the most promising candidates for cellular therapies. Although umbilical cord blood (UCB) is an important source of hematopoietic stem cells, its therapeutic potential goes beyond this, suggesting that solid organ regeneration may potentially be possible. Numerous diverse stem and progenitor cell types have been proposed, with potential ranging from embryoniclike to lineage-committed progenitor cells. Numerous clinical applications for human UCB now suggest MSC. It is nonetheless typical that the idea of UCB conservation is gaining steam even when stem cell therapy is spurring some new research and these cells demonstrate such a benefit to stem cell therapy. The experience detailed here demonstrates, when taken as a whole, that MSCs produced from UCB are viewed as promising therapeutic candidates for a range of human illnesses, including cancer. Considering questions of safety, availability, transplant methodology, rejection, and side effects, it is stated that a therapeutic stem cell transplant employing stem cells from UCB provides a trustworthy repository of early precursor cells that can be helpful in a wide range of different illnesses. We pay particular attention to the ideas of isolation and expansion, phenotyping MSC derived from the UCB, outlining the capacity for differentiation, and finally, the therapeutic potential with regard to stromal support, stemness characteristics, immune modulation, and cancer stem cell therapy. Thus, it provides a summary of the therapeutic uses of MSCs produced from UCB, with a focus on cancer. Additionally, the most recent developments in UCB-derived MSC in cancer research and the present evidence on the double-edged sword of MSCs in cancer treatment will be covered.

REFERENCES

  1. Sayed YF, El Banna HA, Elzorba HY, Galal AM (2019). Application of some nanoparticles in the field of veterinary medicine. Int J Vet Sci Med. 7: 78-93.
  2. Indexed at, Google Scholar, Crossref

  3. Aljabali AA, Bakshi HA, Hakkim FL, Haggag Y, Al Batanyeh MK, et al (2020). Tambuwala Albumin Nano-Encapsulation of Piceatannol Enhances Its Anticancer Potential in Colon Cancer Via Downregulation of Nuclear p65 and HIF-1α Cancers 12.
  4. Indexed at, Google Scholar, Crossref

  5. Oun AA, Shankar S, Rhim JW (2020). Multifunctional nanocellulose metal and metal oxide nanoparticle hybrid nanomaterials. Crit Rev Food Sci Nutr. 60: 435-460.
  6. Indexed at, Google Scholar, Crossref

  7. Yaqoob AA, Ahmad H, Parveen T, Ahmad A, Oves M, et al (2020). Recent advances in metal decorated nanomaterials and their various biological applications: a review. Front Chem. 8.
  8. Indexed at, Google Scholar, Crossref

  9. Ni Q, Zhang F, Liu Y, Wang Z, Yu G, et al (2020). A bi-adjuvant nano vaccine that potentiates immunogenicity of neoantigen for combination immunotherapy of colorectal cancer. Sci Adv. 6.
  10. Indexed at, Google Scholar, Crossref

  11. Renu S, Markazi AD, Dhakal S, Lakshmanappa YS, Shanmugasundaram R, et al (2020).Oral deliverable mucoadhesive chitosan-salmonella subunit nanovaccine for layer chickens. Int J Nanomed Nanosurg. 15: 761-777.
  12. Indexed at, Google Scholar, Crossref

  13. Collins KA, Snaith R, Cottingham MG, Gilbert SC, Hill AVS, et al (2017). Enhancing protective immunity to malaria with a highly immunogenic virus-like particle vaccine. Sci Rep. 7
  14. Indexed at, Google Scholar, Crossref

  15. Xiang SD, Wilson KL, Goubier A, Heyerick A, Plebanski M, et al (2018) Design of peptide-based nanovaccines targeting leading antigens from gynecological cancers to induce HLA-A2.1 restricted CD8+ t cell responses. Front Immunol. 9.
  16. Indexed at, Google Scholar, Crossref

  17. Ding P, Jin Q, Chen X, Yang S, Guo J, et al (2019). Nanovaccine confers dual protection against influenza A virus and porcine circovirus type 2. Int J Nanomed Nanosurg. 14: 7533-7548.
  18. Indexed at, Google Scholar, Crossref

  19. Zhu G, Lynn GM, Jacobson O, Chen K, Liu Y, et al (2017) Albumin/vaccine nanocomplexes that assemble in vivo for combination cancer immunotherapy. Nat Commun. 8.
  20. Indexed at, Google Scholar, Crossref