The potential of interleukin-17 to mediate hematopoietic response
Samo za registrovane korisnike
2012
Članak u časopisu (Objavljena verzija)

Metapodaci
Prikaz svih podataka o dokumentuApstrakt
It has long been known that T cells have the potential to modulate hematopoietic response in different ways. More recently, the importance of interleukin (IL)-17-secreting Th17 cells in T-cell-mediated regulation of hematopoiesis was indicated by the line of evidence that IL-17 links T-cell function and hematopoiesis through stimulation of granulopoiesis and neutrophil trafficking. Furthermore, our data demonstrated that IL-17 also affects other cells of hematopoietic system, such as erythroid progenitors, as well as mesenchymal stem cells. In order to better understand the regulatory role of IL-17 in hematopoiesis, molecular mechanisms underlying the effects of IL-17 on hematopoietic and mesenchymal stem cells were also studied.
Ključne reči:
IL-17 / Hematopoiesis / Myeloid and erythroid progenitors / Bone marrow / SpleenIzvor:
Immunologic Research, 2012, 52, 1-2, 34-41Izdavač:
- Humana Press Inc, Totowa
Finansiranje / projekti:
DOI: 10.1007/s12026-012-8276-8
ISSN: 0257-277X
PubMed: 22392050
WoS: 000303057600005
Scopus: 2-s2.0-84859916452
Institucija/grupa
Institut za medicinska istraživanjaTY - JOUR AU - Krstić, Aleksandra AU - Mojsilović, Slavko AU - Jovčić, Gordana AU - Bugarski, Diana PY - 2012 UR - http://rimi.imi.bg.ac.rs/handle/123456789/392 AB - It has long been known that T cells have the potential to modulate hematopoietic response in different ways. More recently, the importance of interleukin (IL)-17-secreting Th17 cells in T-cell-mediated regulation of hematopoiesis was indicated by the line of evidence that IL-17 links T-cell function and hematopoiesis through stimulation of granulopoiesis and neutrophil trafficking. Furthermore, our data demonstrated that IL-17 also affects other cells of hematopoietic system, such as erythroid progenitors, as well as mesenchymal stem cells. In order to better understand the regulatory role of IL-17 in hematopoiesis, molecular mechanisms underlying the effects of IL-17 on hematopoietic and mesenchymal stem cells were also studied. PB - Humana Press Inc, Totowa T2 - Immunologic Research T1 - The potential of interleukin-17 to mediate hematopoietic response EP - 41 IS - 1-2 SP - 34 VL - 52 DO - 10.1007/s12026-012-8276-8 ER -
@article{ author = "Krstić, Aleksandra and Mojsilović, Slavko and Jovčić, Gordana and Bugarski, Diana", year = "2012", abstract = "It has long been known that T cells have the potential to modulate hematopoietic response in different ways. More recently, the importance of interleukin (IL)-17-secreting Th17 cells in T-cell-mediated regulation of hematopoiesis was indicated by the line of evidence that IL-17 links T-cell function and hematopoiesis through stimulation of granulopoiesis and neutrophil trafficking. Furthermore, our data demonstrated that IL-17 also affects other cells of hematopoietic system, such as erythroid progenitors, as well as mesenchymal stem cells. In order to better understand the regulatory role of IL-17 in hematopoiesis, molecular mechanisms underlying the effects of IL-17 on hematopoietic and mesenchymal stem cells were also studied.", publisher = "Humana Press Inc, Totowa", journal = "Immunologic Research", title = "The potential of interleukin-17 to mediate hematopoietic response", pages = "41-34", number = "1-2", volume = "52", doi = "10.1007/s12026-012-8276-8" }
Krstić, A., Mojsilović, S., Jovčić, G.,& Bugarski, D.. (2012). The potential of interleukin-17 to mediate hematopoietic response. in Immunologic Research Humana Press Inc, Totowa., 52(1-2), 34-41. https://doi.org/10.1007/s12026-012-8276-8
Krstić A, Mojsilović S, Jovčić G, Bugarski D. The potential of interleukin-17 to mediate hematopoietic response. in Immunologic Research. 2012;52(1-2):34-41. doi:10.1007/s12026-012-8276-8 .
Krstić, Aleksandra, Mojsilović, Slavko, Jovčić, Gordana, Bugarski, Diana, "The potential of interleukin-17 to mediate hematopoietic response" in Immunologic Research, 52, no. 1-2 (2012):34-41, https://doi.org/10.1007/s12026-012-8276-8 . .