Milosavljević, Petar

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  • Milosavljević, Petar (5)

Author's Bibliography

Oxidative stress status assessment of rats' brains injury following subacute exposure to K-oximes

Jaćević, Vesna; Dumanović, Jelena; Grujić-Milanović, Jelica; Milovanović, Zoran; Amidžić, Ljiljana; Vojinović, Nataša; Nežić, Lana; Marković, Bojan; Dobričić, Vladimir; Milosavljević, Petar; Nepovimova, Eugenie; Kuča, Kamil

(Elsevier B.V., 2023)


                                            

                                            
Jaćević, V., Dumanović, J., Grujić-Milanović, J., Milovanović, Z., Amidžić, L., Vojinović, N., Nežić, L., Marković, B., Dobričić, V., Milosavljević, P., Nepovimova, E.,& Kuča, K.. (2023). Oxidative stress status assessment of rats' brains injury following subacute exposure to K-oximes. in Chemico-biological interactions
Elsevier B.V.., 383, 110658.
https://doi.org/10.1016/j.cbi.2023.110658
Jaćević V, Dumanović J, Grujić-Milanović J, Milovanović Z, Amidžić L, Vojinović N, Nežić L, Marković B, Dobričić V, Milosavljević P, Nepovimova E, Kuča K. Oxidative stress status assessment of rats' brains injury following subacute exposure to K-oximes. in Chemico-biological interactions. 2023;383:110658.
doi:10.1016/j.cbi.2023.110658 .
Jaćević, Vesna, Dumanović, Jelena, Grujić-Milanović, Jelica, Milovanović, Zoran, Amidžić, Ljiljana, Vojinović, Nataša, Nežić, Lana, Marković, Bojan, Dobričić, Vladimir, Milosavljević, Petar, Nepovimova, Eugenie, Kuča, Kamil, "Oxidative stress status assessment of rats' brains injury following subacute exposure to K-oximes" in Chemico-biological interactions, 383 (2023):110658,
https://doi.org/10.1016/j.cbi.2023.110658 . .

Disulfiram moderately restores impaired hepatic redox status of rats subchronically exposed to cadmium

Begić, Aida; Đurić, Ana; Ninković, Milica; Stevanović, Ivana; Đurđević, Dragan; Pavlović, Miloš; Jelić, Katarina; Pantelić, Ana; Zebić, Goran; Dejanović, Bratislav; Stanojević, Ivan; Vojvodić, Danilo; Milosavljević, Petar; Đukić, Mirjana; Saso, Luciano

(Taylor & Francis Ltd, Abingdon, 2017)

TY  - JOUR
AU  - Begić, Aida
AU  - Đurić, Ana
AU  - Ninković, Milica
AU  - Stevanović, Ivana
AU  - Đurđević, Dragan
AU  - Pavlović, Miloš
AU  - Jelić, Katarina
AU  - Pantelić, Ana
AU  - Zebić, Goran
AU  - Dejanović, Bratislav
AU  - Stanojević, Ivan
AU  - Vojvodić, Danilo
AU  - Milosavljević, Petar
AU  - Đukić, Mirjana
AU  - Saso, Luciano
PY  - 2017
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/2963
AB  - Examination of cadmium (Cd) toxicity and disulfiram (DSF) effect on liver was focused on oxidative stress (OS), bioelements status, morphological and functional changes. Male Wistar rats were intraperitoneally treated with 1mg CdCl2/kg BW/day; orally with 178.5 mg DSF/kg BW/day for 1, 3, 10 and 21 days; and co-exposed from 22nd to 42nd day. The co-exposure nearly restored previously suppressed total superoxide dismutase (SOD), catalase (CAT) and increased glutathione peroxidase (GPx) activities; increased previously reduced glutathione reductase (GR) and total glutathione-S-transferase (GST) activities; reduced previously increased superoxide anion radical (O-2(center dot-)) and malondialdehyde (MDA) levels; increased zinc (Zn) and iron (Fe), and decreased copper (Cu) (yet above control value), while magnesium (Mg) was not affected; and decreased serum alanine aminotransferases (ALT) levels. Histopathological examination showed signs of inflammation process as previously demonstrated by exposure to Cd. Overall, we ascertained partial liver redox status improvement, compared with the formerly Cd-induced impact.
PB  - Taylor & Francis Ltd, Abingdon
T2  - Journal of Enzyme Inhibition and Medicinal Chemistry
T1  - Disulfiram moderately restores impaired hepatic redox status of rats subchronically exposed to cadmium
VL  - 32
IS  - 1
SP  - 478
EP  - 489
DO  - 10.1080/14756366.2016.1261132
ER  - 
@article{
author = "Begić, Aida and Đurić, Ana and Ninković, Milica and Stevanović, Ivana and Đurđević, Dragan and Pavlović, Miloš and Jelić, Katarina and Pantelić, Ana and Zebić, Goran and Dejanović, Bratislav and Stanojević, Ivan and Vojvodić, Danilo and Milosavljević, Petar and Đukić, Mirjana and Saso, Luciano",
year = "2017",
abstract = "Examination of cadmium (Cd) toxicity and disulfiram (DSF) effect on liver was focused on oxidative stress (OS), bioelements status, morphological and functional changes. Male Wistar rats were intraperitoneally treated with 1mg CdCl2/kg BW/day; orally with 178.5 mg DSF/kg BW/day for 1, 3, 10 and 21 days; and co-exposed from 22nd to 42nd day. The co-exposure nearly restored previously suppressed total superoxide dismutase (SOD), catalase (CAT) and increased glutathione peroxidase (GPx) activities; increased previously reduced glutathione reductase (GR) and total glutathione-S-transferase (GST) activities; reduced previously increased superoxide anion radical (O-2(center dot-)) and malondialdehyde (MDA) levels; increased zinc (Zn) and iron (Fe), and decreased copper (Cu) (yet above control value), while magnesium (Mg) was not affected; and decreased serum alanine aminotransferases (ALT) levels. Histopathological examination showed signs of inflammation process as previously demonstrated by exposure to Cd. Overall, we ascertained partial liver redox status improvement, compared with the formerly Cd-induced impact.",
publisher = "Taylor & Francis Ltd, Abingdon",
journal = "Journal of Enzyme Inhibition and Medicinal Chemistry",
title = "Disulfiram moderately restores impaired hepatic redox status of rats subchronically exposed to cadmium",
volume = "32",
number = "1",
pages = "478-489",
doi = "10.1080/14756366.2016.1261132"
}
Begić, A., Đurić, A., Ninković, M., Stevanović, I., Đurđević, D., Pavlović, M., Jelić, K., Pantelić, A., Zebić, G., Dejanović, B., Stanojević, I., Vojvodić, D., Milosavljević, P., Đukić, M.,& Saso, L.. (2017). Disulfiram moderately restores impaired hepatic redox status of rats subchronically exposed to cadmium. in Journal of Enzyme Inhibition and Medicinal Chemistry
Taylor & Francis Ltd, Abingdon., 32(1), 478-489.
https://doi.org/10.1080/14756366.2016.1261132
Begić A, Đurić A, Ninković M, Stevanović I, Đurđević D, Pavlović M, Jelić K, Pantelić A, Zebić G, Dejanović B, Stanojević I, Vojvodić D, Milosavljević P, Đukić M, Saso L. Disulfiram moderately restores impaired hepatic redox status of rats subchronically exposed to cadmium. in Journal of Enzyme Inhibition and Medicinal Chemistry. 2017;32(1):478-489.
doi:10.1080/14756366.2016.1261132 .
Begić, Aida, Đurić, Ana, Ninković, Milica, Stevanović, Ivana, Đurđević, Dragan, Pavlović, Miloš, Jelić, Katarina, Pantelić, Ana, Zebić, Goran, Dejanović, Bratislav, Stanojević, Ivan, Vojvodić, Danilo, Milosavljević, Petar, Đukić, Mirjana, Saso, Luciano, "Disulfiram moderately restores impaired hepatic redox status of rats subchronically exposed to cadmium" in Journal of Enzyme Inhibition and Medicinal Chemistry, 32, no. 1 (2017):478-489,
https://doi.org/10.1080/14756366.2016.1261132 . .
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Oxidative stress in rat kidneys due to 3,4-methylenedioxymetamphetamine (ecstasy) toxicity

Ninković, Milica; Selaković, Vesna; Đukić, Mirjana; Milosavljević, Petar; Vasiljević, Ivana; Jovanović, Marina; Maličević, Živorad

(Wiley, Hoboken, 2008)

TY  - JOUR
AU  - Ninković, Milica
AU  - Selaković, Vesna
AU  - Đukić, Mirjana
AU  - Milosavljević, Petar
AU  - Vasiljević, Ivana
AU  - Jovanović, Marina
AU  - Maličević, Živorad
PY  - 2008
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/1060
AB  - Aim: The mechanism of MDMA (3,4-methylenedioxymethamphetamine)-induced toxicity is believed to be, in part, due to enhanced oxidative stress. As MDMA is eliminated via the kidney, the aim. of this study was to investigate whether MDMA created conditions of oxidative stress within rat kidney. Methods: Adult male Wistar rats were divided into three groups, control treatment (water), acute MDMA administration (single oral dose: 5, 10, 20 or 40 mg/kg body weight) and subacute MDMA administration (5, 10, or 20 mg/kg body weight per day during 14 days). Animals were sacrificed 8 h after the single oral MDMA administration in the acute MDMA administration group and after the last MDMA administration in the subacute MDMA administration group. Rectal temperature measurements, oxidative stress status parameters and histological examinations were performed. Results: In all MDMA-administered rats, rectal temperature markedly increased peaking approximately 1 h after MDMA ingestion. Superoxide dismutase activity and thiobarbituric acid reactive substances increased after MDMA administration. Histological examinations of the kidney revealed dose-dependent disruption of tissue structure in subacute MDMA-administered rats. The latter was not observed in acute MDMA-administered rats.
PB  - Wiley, Hoboken
T2  - Nephrology
T1  - Oxidative stress in rat kidneys due to 3,4-methylenedioxymetamphetamine (ecstasy) toxicity
VL  - 13
IS  - 1
SP  - 33
EP  - 37
DO  - 10.1111/j.1440-1797.2007.00886.x
ER  - 
@article{
author = "Ninković, Milica and Selaković, Vesna and Đukić, Mirjana and Milosavljević, Petar and Vasiljević, Ivana and Jovanović, Marina and Maličević, Živorad",
year = "2008",
abstract = "Aim: The mechanism of MDMA (3,4-methylenedioxymethamphetamine)-induced toxicity is believed to be, in part, due to enhanced oxidative stress. As MDMA is eliminated via the kidney, the aim. of this study was to investigate whether MDMA created conditions of oxidative stress within rat kidney. Methods: Adult male Wistar rats were divided into three groups, control treatment (water), acute MDMA administration (single oral dose: 5, 10, 20 or 40 mg/kg body weight) and subacute MDMA administration (5, 10, or 20 mg/kg body weight per day during 14 days). Animals were sacrificed 8 h after the single oral MDMA administration in the acute MDMA administration group and after the last MDMA administration in the subacute MDMA administration group. Rectal temperature measurements, oxidative stress status parameters and histological examinations were performed. Results: In all MDMA-administered rats, rectal temperature markedly increased peaking approximately 1 h after MDMA ingestion. Superoxide dismutase activity and thiobarbituric acid reactive substances increased after MDMA administration. Histological examinations of the kidney revealed dose-dependent disruption of tissue structure in subacute MDMA-administered rats. The latter was not observed in acute MDMA-administered rats.",
publisher = "Wiley, Hoboken",
journal = "Nephrology",
title = "Oxidative stress in rat kidneys due to 3,4-methylenedioxymetamphetamine (ecstasy) toxicity",
volume = "13",
number = "1",
pages = "33-37",
doi = "10.1111/j.1440-1797.2007.00886.x"
}
Ninković, M., Selaković, V., Đukić, M., Milosavljević, P., Vasiljević, I., Jovanović, M.,& Maličević, Ž.. (2008). Oxidative stress in rat kidneys due to 3,4-methylenedioxymetamphetamine (ecstasy) toxicity. in Nephrology
Wiley, Hoboken., 13(1), 33-37.
https://doi.org/10.1111/j.1440-1797.2007.00886.x
Ninković M, Selaković V, Đukić M, Milosavljević P, Vasiljević I, Jovanović M, Maličević Ž. Oxidative stress in rat kidneys due to 3,4-methylenedioxymetamphetamine (ecstasy) toxicity. in Nephrology. 2008;13(1):33-37.
doi:10.1111/j.1440-1797.2007.00886.x .
Ninković, Milica, Selaković, Vesna, Đukić, Mirjana, Milosavljević, Petar, Vasiljević, Ivana, Jovanović, Marina, Maličević, Živorad, "Oxidative stress in rat kidneys due to 3,4-methylenedioxymetamphetamine (ecstasy) toxicity" in Nephrology, 13, no. 1 (2008):33-37,
https://doi.org/10.1111/j.1440-1797.2007.00886.x . .
12
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Immunomodulation of experimental autoimmune myocarditis by pentoxifylline

Milenković, Marina; Milosavljević, Petar; Stojić-Vukanić, Zorica; Dimitrijević, Miroslava; Čolić, Miodrag

(Savez farmaceutskih udruženja Srbije, Beograd, 2004)

TY  - JOUR
AU  - Milenković, Marina
AU  - Milosavljević, Petar
AU  - Stojić-Vukanić, Zorica
AU  - Dimitrijević, Miroslava
AU  - Čolić, Miodrag
PY  - 2004
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/501
AB  - We designed the present study to provide evidence of the immunomodulatory effects of pentoxifylline (PTX) in experimental autoimmune myocarditis (EAM) in rats. PTX is xantine-derived agent known to inhibit the production of TNF-α and his beneficial effects have been reported in patients with dilated cardiomyopathy. In this study we examined the efficacy of PTX in the treatment of experimental autoimmune myocarditis as a paradigm of the autoimmune mechanisms involved in pathogenesis of dilated cardiomiopathy. Male DA rats immunized with porcine cardiac myosin were treated i.m. with PTX (200 mg/kg/day) over 7 days, begenning either on the day of immunization (early treatment group), or on day 14. postimmunization (late treatment group). Disease course and severity were evaluated by macroscopic score of the heart, heart weight/body weight ratio (Hw/Bw), histological and immunohistochemical analysis of cardiac tisssue. We found in our study that PTX exhibited both preventive and therapeutical effects in EAM.
AB  - U radu je ispitivan uticaj pentoksifilina (PTX) na razvoj i tok eksperimentalnog autoimunog miokarditisa pacova. Pentoksifilin je derivat ksantina sa inhibitornim efektom na produkciju TNF-α, a klinički je potvrđen i njegov pozitivan učinak u terapiji pacijenata sa dilatacionom kardiomiopatijom. U ispitivanju je testiran imunomodulatorni efekat PTX u tretmanu eksperimentalnog autoimunog miokarditisa koji predstavlja eksperimentalni model za proučavanje autoimunskih mehanizama uključenih u razvoj dilatacione kardiomiopatije. Pacovi DA soja imunizovani srčanim miozinom tretirani su pentoksifilinom u dozi od 200 mg/kg t.m., počev od 0.-6. dana (rani tretman), ili od 14.-20. dana (kasni tretman) u odnosu na termin imunizacije miozinom. Razvoj i intenzitet miokarditisa praćeni su analizom makroskopskih karakteristika srca, indeksa masa srca/telesna masa (Hwt/Bwt), histoloških i imunohistohemijskih analiza miokarda. Dobijeni rezultati su pokazali da PTX ispoljava profilaktičan i terapijski učinak u eksperimentalnom autoimunom miokarditisu.
PB  - Savez farmaceutskih udruženja Srbije, Beograd
T2  - Arhiv za farmaciju
T1  - Immunomodulation of experimental autoimmune myocarditis by pentoxifylline
T1  - Autoimunskog miokarditisa primenom pentoksifilina
VL  - 54
IS  - 6
SP  - 761
EP  - 771
UR  - https://hdl.handle.net/21.15107/rcub_farfar_501
ER  - 
@article{
author = "Milenković, Marina and Milosavljević, Petar and Stojić-Vukanić, Zorica and Dimitrijević, Miroslava and Čolić, Miodrag",
year = "2004",
abstract = "We designed the present study to provide evidence of the immunomodulatory effects of pentoxifylline (PTX) in experimental autoimmune myocarditis (EAM) in rats. PTX is xantine-derived agent known to inhibit the production of TNF-α and his beneficial effects have been reported in patients with dilated cardiomyopathy. In this study we examined the efficacy of PTX in the treatment of experimental autoimmune myocarditis as a paradigm of the autoimmune mechanisms involved in pathogenesis of dilated cardiomiopathy. Male DA rats immunized with porcine cardiac myosin were treated i.m. with PTX (200 mg/kg/day) over 7 days, begenning either on the day of immunization (early treatment group), or on day 14. postimmunization (late treatment group). Disease course and severity were evaluated by macroscopic score of the heart, heart weight/body weight ratio (Hw/Bw), histological and immunohistochemical analysis of cardiac tisssue. We found in our study that PTX exhibited both preventive and therapeutical effects in EAM., U radu je ispitivan uticaj pentoksifilina (PTX) na razvoj i tok eksperimentalnog autoimunog miokarditisa pacova. Pentoksifilin je derivat ksantina sa inhibitornim efektom na produkciju TNF-α, a klinički je potvrđen i njegov pozitivan učinak u terapiji pacijenata sa dilatacionom kardiomiopatijom. U ispitivanju je testiran imunomodulatorni efekat PTX u tretmanu eksperimentalnog autoimunog miokarditisa koji predstavlja eksperimentalni model za proučavanje autoimunskih mehanizama uključenih u razvoj dilatacione kardiomiopatije. Pacovi DA soja imunizovani srčanim miozinom tretirani su pentoksifilinom u dozi od 200 mg/kg t.m., počev od 0.-6. dana (rani tretman), ili od 14.-20. dana (kasni tretman) u odnosu na termin imunizacije miozinom. Razvoj i intenzitet miokarditisa praćeni su analizom makroskopskih karakteristika srca, indeksa masa srca/telesna masa (Hwt/Bwt), histoloških i imunohistohemijskih analiza miokarda. Dobijeni rezultati su pokazali da PTX ispoljava profilaktičan i terapijski učinak u eksperimentalnom autoimunom miokarditisu.",
publisher = "Savez farmaceutskih udruženja Srbije, Beograd",
journal = "Arhiv za farmaciju",
title = "Immunomodulation of experimental autoimmune myocarditis by pentoxifylline, Autoimunskog miokarditisa primenom pentoksifilina",
volume = "54",
number = "6",
pages = "761-771",
url = "https://hdl.handle.net/21.15107/rcub_farfar_501"
}
Milenković, M., Milosavljević, P., Stojić-Vukanić, Z., Dimitrijević, M.,& Čolić, M.. (2004). Immunomodulation of experimental autoimmune myocarditis by pentoxifylline. in Arhiv za farmaciju
Savez farmaceutskih udruženja Srbije, Beograd., 54(6), 761-771.
https://hdl.handle.net/21.15107/rcub_farfar_501
Milenković M, Milosavljević P, Stojić-Vukanić Z, Dimitrijević M, Čolić M. Immunomodulation of experimental autoimmune myocarditis by pentoxifylline. in Arhiv za farmaciju. 2004;54(6):761-771.
https://hdl.handle.net/21.15107/rcub_farfar_501 .
Milenković, Marina, Milosavljević, Petar, Stojić-Vukanić, Zorica, Dimitrijević, Miroslava, Čolić, Miodrag, "Immunomodulation of experimental autoimmune myocarditis by pentoxifylline" in Arhiv za farmaciju, 54, no. 6 (2004):761-771,
https://hdl.handle.net/21.15107/rcub_farfar_501 .

Differentiation of human dendritic cells from monocytes in vitro using granulocyte-macrophage colony stimulating factor and low concentration of interleukin-4

Čolić, Miodrag; Jandrić, Dušan; Stojić-Vukanić, Zorica; Antić-Stanković, Jelena; Popović, Petar; Vasilijić, Saša; Milosavljević, Petar; Balint, Bela

(Vojnomedicinska akademija - Institut za naučne informacije, Beograd, 2003)

TY  - JOUR
AU  - Čolić, Miodrag
AU  - Jandrić, Dušan
AU  - Stojić-Vukanić, Zorica
AU  - Antić-Stanković, Jelena
AU  - Popović, Petar
AU  - Vasilijić, Saša
AU  - Milosavljević, Petar
AU  - Balint, Bela
PY  - 2003
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/465
AB  - Several laboratories have developed culture systems that allow the generation of large numbers of human dendritic cells (DC) from monocytes using granulocyte-macrophage colony stimulating factor (GM-CSF), and interleukin-4 (IL-4). In this work we provided evidence that GM-CSF (100 ng/ml) in combination with a low concentration of IL-4 (5 ng/ml) was efficient in the generation of immature, non-adherent, monocyte-derived DC as the same concentration of GM-CSF, and ten times higher concentration of IL-4 (50 ng/ml). This conclusion was based on the similar phenotype profile of DC such as the expression of CD1a, CD80, CD86, and HLA-DR, down-regulation of CD14, and the absence of CD83, as well as on their similar allostimulatory activity for T cells. A higher number of cells remained adherent in cultures with lower concentrations of IL-4 than in cultures with higher concentrations of the cytokine. However, most of these adherent cells down-regulated CD14 and stimulated the proliferation of alloreactive T cells. In contrast adherent cells cultivated with GM-CSF alone were predominantly macrophages as judged by the expression of CD14 and the inefficiency to stimulate alloreactive T cells. DC generated in the presence of lower concentrations of IL-4 had higher proapoptotic potential for the Jurkat cell line than DC differentiated with higher concentrations of IL-4, suggesting their stronger cytotoxic, anti-tumor effect.
AB  - U više laboratorija su uspostavljeni sistemi za kultivaciju velikog broja humanih dendritičnih ćelija (DĆ) od monocita korišćenjem faktora stimulacije granulocitno--makrofagnih kolonija (GM-CSF) i interleukina-4 (IL-4). U ovom radu je pokazano da je kombinacija GM-CSF (100 ng/ml) i mala koncentracija IL-4 (5 ng/ml) podjednako efikasna za dobijanje nezrelih, neadherentnih, DĆ monocitnog porekla kao i kombinacija GM-CSF sa deset puta većom koncentracijom IL-4 (50 ng/ml). Ovaj zaključak izveden je na osnovu sličnog fenotipskog profila DĆ (ispoljavanje CD1a, CD80, CD86 i HLA-DR, smanjenje ekspresije CD14 i odsustva CD83), kao i slične alostimulatorne aktivnosti ovih ćelija za limfocite T. U kulturama sa nižim koncentracijama IL-4 prisutan je bio veći broj adherentnih ćelija nego u kulturama sa većim koncentracijama IL-4. Međutim, većina ovih ćelija je smanjivala ekspresiju CD14 i stimulisala proliferaciju aloreaktivnih limfocita T. Nasuprot njima adherentne ćelije, diferentovane samo u prisustvu GM-CSF, koje su ispoljavale CD14 i nisu imale sposobnost stimulacije aloreakativnih limfocita T pokazivale su karakteristike makrofaga. DĆ obrazovane u prisustvu manjih koncentracija IL-4 imale su veći potencijal za indukciju apoptoze Jurkat ćelijske linije, a time i snažniji citotoksični, antitumorski efekat nego DĆ diferentovane u prisustvu većih koncentracija IL-4.
PB  - Vojnomedicinska akademija - Institut za naučne informacije, Beograd
T2  - Vojnosanitetski pregled
T1  - Differentiation of human dendritic cells from monocytes in vitro using granulocyte-macrophage colony stimulating factor and low concentration of interleukin-4
T1  - Diferencijacija humanih dendritičnih ćelija od monocita in vitro korišćenjem faktora stimulacije granulocitno-makrofagnih kolonija i niske koncentracije interleukina-4
VL  - 60
IS  - 5
SP  - 531
EP  - 538
DO  - 10.2298/VSP0305531C
ER  - 
@article{
author = "Čolić, Miodrag and Jandrić, Dušan and Stojić-Vukanić, Zorica and Antić-Stanković, Jelena and Popović, Petar and Vasilijić, Saša and Milosavljević, Petar and Balint, Bela",
year = "2003",
abstract = "Several laboratories have developed culture systems that allow the generation of large numbers of human dendritic cells (DC) from monocytes using granulocyte-macrophage colony stimulating factor (GM-CSF), and interleukin-4 (IL-4). In this work we provided evidence that GM-CSF (100 ng/ml) in combination with a low concentration of IL-4 (5 ng/ml) was efficient in the generation of immature, non-adherent, monocyte-derived DC as the same concentration of GM-CSF, and ten times higher concentration of IL-4 (50 ng/ml). This conclusion was based on the similar phenotype profile of DC such as the expression of CD1a, CD80, CD86, and HLA-DR, down-regulation of CD14, and the absence of CD83, as well as on their similar allostimulatory activity for T cells. A higher number of cells remained adherent in cultures with lower concentrations of IL-4 than in cultures with higher concentrations of the cytokine. However, most of these adherent cells down-regulated CD14 and stimulated the proliferation of alloreactive T cells. In contrast adherent cells cultivated with GM-CSF alone were predominantly macrophages as judged by the expression of CD14 and the inefficiency to stimulate alloreactive T cells. DC generated in the presence of lower concentrations of IL-4 had higher proapoptotic potential for the Jurkat cell line than DC differentiated with higher concentrations of IL-4, suggesting their stronger cytotoxic, anti-tumor effect., U više laboratorija su uspostavljeni sistemi za kultivaciju velikog broja humanih dendritičnih ćelija (DĆ) od monocita korišćenjem faktora stimulacije granulocitno--makrofagnih kolonija (GM-CSF) i interleukina-4 (IL-4). U ovom radu je pokazano da je kombinacija GM-CSF (100 ng/ml) i mala koncentracija IL-4 (5 ng/ml) podjednako efikasna za dobijanje nezrelih, neadherentnih, DĆ monocitnog porekla kao i kombinacija GM-CSF sa deset puta većom koncentracijom IL-4 (50 ng/ml). Ovaj zaključak izveden je na osnovu sličnog fenotipskog profila DĆ (ispoljavanje CD1a, CD80, CD86 i HLA-DR, smanjenje ekspresije CD14 i odsustva CD83), kao i slične alostimulatorne aktivnosti ovih ćelija za limfocite T. U kulturama sa nižim koncentracijama IL-4 prisutan je bio veći broj adherentnih ćelija nego u kulturama sa većim koncentracijama IL-4. Međutim, većina ovih ćelija je smanjivala ekspresiju CD14 i stimulisala proliferaciju aloreaktivnih limfocita T. Nasuprot njima adherentne ćelije, diferentovane samo u prisustvu GM-CSF, koje su ispoljavale CD14 i nisu imale sposobnost stimulacije aloreakativnih limfocita T pokazivale su karakteristike makrofaga. DĆ obrazovane u prisustvu manjih koncentracija IL-4 imale su veći potencijal za indukciju apoptoze Jurkat ćelijske linije, a time i snažniji citotoksični, antitumorski efekat nego DĆ diferentovane u prisustvu većih koncentracija IL-4.",
publisher = "Vojnomedicinska akademija - Institut za naučne informacije, Beograd",
journal = "Vojnosanitetski pregled",
title = "Differentiation of human dendritic cells from monocytes in vitro using granulocyte-macrophage colony stimulating factor and low concentration of interleukin-4, Diferencijacija humanih dendritičnih ćelija od monocita in vitro korišćenjem faktora stimulacije granulocitno-makrofagnih kolonija i niske koncentracije interleukina-4",
volume = "60",
number = "5",
pages = "531-538",
doi = "10.2298/VSP0305531C"
}
Čolić, M., Jandrić, D., Stojić-Vukanić, Z., Antić-Stanković, J., Popović, P., Vasilijić, S., Milosavljević, P.,& Balint, B.. (2003). Differentiation of human dendritic cells from monocytes in vitro using granulocyte-macrophage colony stimulating factor and low concentration of interleukin-4. in Vojnosanitetski pregled
Vojnomedicinska akademija - Institut za naučne informacije, Beograd., 60(5), 531-538.
https://doi.org/10.2298/VSP0305531C
Čolić M, Jandrić D, Stojić-Vukanić Z, Antić-Stanković J, Popović P, Vasilijić S, Milosavljević P, Balint B. Differentiation of human dendritic cells from monocytes in vitro using granulocyte-macrophage colony stimulating factor and low concentration of interleukin-4. in Vojnosanitetski pregled. 2003;60(5):531-538.
doi:10.2298/VSP0305531C .
Čolić, Miodrag, Jandrić, Dušan, Stojić-Vukanić, Zorica, Antić-Stanković, Jelena, Popović, Petar, Vasilijić, Saša, Milosavljević, Petar, Balint, Bela, "Differentiation of human dendritic cells from monocytes in vitro using granulocyte-macrophage colony stimulating factor and low concentration of interleukin-4" in Vojnosanitetski pregled, 60, no. 5 (2003):531-538,
https://doi.org/10.2298/VSP0305531C . .
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