Title
Involvement of P2 receptors in hematopoiesis and hematopoietic disorders, and as pharmacological targets
Date Issued
01 March 2020
Access level
open access
Resource Type
review
Author(s)
Filippin K.J.
de Souza K.F.S.
de Araujo Júnior R.T.
Torquato H.F.V.
Dias D.A.
Parisotto E.B.
Ferreira A.T.
Universidade Federal de Mato Grosso do Sul
Publisher(s)
Springer
Abstract
Several reports have shown the presence of P2 receptors in hematopoietic stem cells (HSCs). These receptors are activated by extracellular nucleotides released from different sources. In the hematopoietic niche, the release of purines and pyrimidines in the milieu by lytic and nonlytic mechanisms has been described. The expression of P2 receptors from HSCs until maturity is still intriguing scientists. Several reports have shown the participation of P2 receptors in events associated with modulation of the immune system, but their participation in other physiological processes is under investigation. The presence of P2 receptors in HSCs and their ability to modulate this population have awakened interest in exploring the involvement of P2 receptors in hematopoiesis and their participation in hematopoietic disorders. Among the P2 receptors, the receptor P2X7 is of particular interest, because of its different roles in hematopoietic cells (e.g., infection, inflammation, cell death and survival, leukemias and lymphomas), making the P2X7 receptor a promising pharmacological target. Additionally, the role of P2Y12 receptor in platelet activation has been well-documented and is the main example of the importance of the pharmacological modulation of P2 receptor activity. In this review, we focus on the role of P2 receptors in the hematopoietic system, addressing these receptors as potential pharmacological targets.
Volume
16
Issue
1
Language
English
OCDE Knowledge area
Bioquímica, Biología molecular
Subjects
Scopus EID
2-s2.0-85077024717
PubMed ID
Source
Purinergic Signalling
ISSN of the container
15739538
Sponsor(s)
This publication and the previous related results were supported by “Fundação de Amparo à Pesquisa do Estado de São Paulo” (FAPESP. Proc. 2018/23870-4) and “Conselho Nacional de Desenvolvimento Científico e Tecnológico” (CNPq 425965/2018-0).
Sources of information:
Directorio de Producción Científica
Scopus