Rahmah Zainabur, Wahju-Sardjono Teguh, Enggar-Fitri Loeki, Ulfiati Adilah, Ungu Bougenvil, Zulhaidah-Arthamin Maimun, Norahmawati Eviana
Laboratory of Parasitology, Faculty of Medicine and Health Sciences, Universitas Islam Negeri Maulana Malik Ibrahim, Malang, Indonesia.
Department of Parasitology, Malaria Research Group, Faculty of Medicine, Universitas Brawijaya, Malang, Indonesia.
Iran J Parasitol. 2019 Oct-Dec;14(4):604-613.
Placental malaria involves the sequestration of infected erythrocytes and infiltration of monocytes, helper T cells (CD4), cytotoxic T cells (CD8) as well as T-cell intracellular antigen-1 (TIA-1) in placental intervillous space. These may interferes the nutrient and oxygen transport, causing placental hypoxia and insufficiency that may affect the fetal growth. This study aimed to prove whether the infiltration of lymphocytes in placental malaria mice increases the expression of HIF-1α thus causes fetal Low Birth Weight (LBW).
Nine pregnant BALB/c mice that infected with ANKA strain on day 9 post mating were used as treatment group and 8 non infected pregnant mice were used as control group. The mice were sacrificed on day 18 post mating; then the fetus was weighed individually and the placentas were isolated separately. Expression of CD4, CD8 and HIF-1α were counted by immunohistochemistry using CD4 monoclonal Ab (Santa cruz, sc-59031 CD4) and CD 8 monoclonal Ab (NeoMarker RM-9116-S0) as well as anti-HIF-1α antibody (H1α67) ChIP Grade from Abcam.
There was a higher expression of CD8, CD4 and HIF-1α in infected placenta compare to normal placenta. Analysis using Structural Equation Modeling (SEM) showed expression CD8 and CD4 caused an increase expression of HIF-1α in placenta (t ≥1.96). Expression of HIF-1α caused low fetal weight (t ≥1.96).
In placental malaria, the expression of CD4 and CD8 induce placental hypoxia characterized by increased expression of HIF-1α that causes LBW.
胎盘疟疾涉及感染红细胞的滞留以及单核细胞、辅助性T细胞(CD4)、细胞毒性T细胞(CD8)和T细胞细胞内抗原-1(TIA-1)浸润至胎盘绒毛间隙。这些可能会干扰营养物质和氧气的运输,导致胎盘缺氧和功能不全,进而可能影响胎儿生长。本研究旨在证实胎盘疟疾小鼠中淋巴细胞浸润是否会增加缺氧诱导因子-1α(HIF-1α)的表达,从而导致胎儿低出生体重(LBW)。
将9只在交配后第9天感染ANKA株的怀孕BALB/c小鼠作为治疗组,8只未感染的怀孕小鼠作为对照组。在交配后第18天处死小鼠;然后分别称量胎儿体重并分离胎盘。使用CD4单克隆抗体(圣克鲁斯,sc-59031 CD4)、CD8单克隆抗体(NeoMarker RM-9116-S0)以及来自艾博抗公司的ChIP级抗HIF-1α抗体(H1α67),通过免疫组织化学法计数CD4、CD8和HIF-1α的表达。
与正常胎盘相比,感染胎盘的CD8、CD4和HIF-1α表达更高。使用结构方程模型(SEM)分析表明,CD8和CD4的表达导致胎盘中HIF-1α表达增加(t≥1.96)。HIF-1α的表达导致胎儿体重降低(t≥1.96)。
在胎盘疟疾中,CD4和CD8的表达诱导以HIF-1α表达增加为特征的胎盘缺氧,进而导致低出生体重。