Details

Autor(en) / Beteiligte

• Musaya, Janelisa
• Matovu, Enock
• Senga, Edward
• Nyirenda, Moffat
• Chisi, John

Titel

AcSDKP is down-regulated in anaemia induced by Trypanosoma brucei infection in mice

Ist Teil von

• Malawi medical journal, 2017-09, Vol.29 (3), p.259-264

Ort / Verlag

Malawi: The Medical Association Of Malawi

Erscheinungsjahr

2017

Quelle

MEDLINE

Beschreibungen/Notizen

• Anaemia commonly results from destruction of erythrocytes in the peripheral blood and failure of the bone marrow haematopoietic cells to replenish the erythrocytes. The mechanisms involved in trypanosoma-induced anaemia, including the role of the bone marrow haematopoietic cells are incompletely understood. We studied the responses of a tetrapeptide, AcSDKP, and IL-10, and their association with bone marrow nucleated cells in a GVR35 experimental infection model. Mouse infection was done intraperitoneally with 1 × 10 trypanosomes/mL. Mice were either infected or left uninfected (N = 100). At days 0, 9, 16, 23, 30, 37, and 44 post-infection, mice were euthanised and blood was collected by cardiac puncture to examine for parasitaemia and packed cell volume (PCV) and then centrifuged for plasma, which was used for cytokine ELISA. The mice's femurs were also dissected and bone marrow was collected for femur cellularity. PCV dropped from 39.6% to 27% in infected animals by day 9 and remained low (relative to uninfected mice) for the duration of the experiment. AcSDKP levels decreased from day 0 (11.5 × 10 pg/mL) to day 16 (10 × 10 ), and increased by day 30 (12.6 × 10 ). There was a significant difference at day 16 (P = 0.023) between the infected and uninfected groups. By contrast, expression of IL-10 markedly increased between day 0 (18.6 pg/mL) and day 16 (145 pg/mL) and decreased by day 30 (42.8 pg/mL). There was also a significant difference in IL-10 expression between infected and uninfected mice at day 16 (P < 0.001). Bone marrow nucleated cells were significantly reduced during periods of low plasma AcSDKP and high plasma IL-10 concentrations (5.4 × 10 infected vs 6.2 × 10 on day 0 and 4.9 × 10 infected vs 10 × 10 uninfected on day 16). These data unravel a possible negative feedback interaction between AcSDKP and IL-10 in trypanosome infection. More importantly, this study implicates an IL-10/AcSDKP cytokine network in the regulation of bone marrow nucleated cells and provides a new potential mechanism in the pathogenesis of trypanosoma-induced anaemia. Further mechanistic blocking experiments on AcSDKP and IL-10 are recommended to further clarify understanding of the interaction.