Department of Neuroscience and Physiology, SUNY Upstate Medical University, Syracuse, NY, USA.
Laboratory of Immunopsychiatry, Neuroscience Research Australia, Sydney, NSW, Australia; Discipline of Psychiatry and Mental Health, University of New South Wales, Sydney, NSW, Australia; Monash Institute of Pharmaceutical Science, Monash University, Parkville, VIC, Australia.
Brain Behav Immun. 2023 Jul;111:186-201. doi: 10.1016/j.bbi.2023.03.015. Epub 2023 Mar 21.
In addition to their traditional roles in immune cell communication, cytokines regulate brain development. Cytokines are known to influence neural cell generation, differentiation, maturation, and survival. However, most work on the role of cytokines in brain development investigates rodents or focuses on prenatal events. Here, we investigate how mRNA and protein levels of key cytokines and cytokine receptors change during postnatal development of the human prefrontal cortex. We find that most cytokine transcripts investigated (IL1B, IL18, IL6, TNF, IL13) are lowest at birth and increase between 1.5 and 5 years old. After 5 years old, transcriptional patterns proceeded in one of two directions: decreased expression in teens and young adults (IL1B, p = 0.002; and IL18, p = 0.004) or increased mean expression with maturation, particularly in teenagers (IL6, p = 0.004; TNF, p = 0.002; IL13, p < 0.001). In contrast, cytokine proteins tended to remain elevated after peaking significantly around 3 years of age (IL1B, p = 0.012; IL18, p = 0.026; IL6, p = 0.039; TNF, p < 0.001), with TNF protein being highest in teenagers. An mRNA-only analysis of cytokine receptor transcripts found that early developmental increases in cytokines were paralleled by increases in their ligand-binding receptor subunits, such as IL1R1 (p = 0.033) and IL6R (p < 0.001) transcripts. In contrast, cytokine receptor-associated signaling subunits, IL1RAP and IL6ST, did not change significantly between age groups. Of the two TNF receptors, the 'pro-death' TNFRSF1A and 'pro-survival' TNFRSF1B, only TNFRSF1B was significantly changed (p = 0.028), increasing first in toddlers and again in young adults. Finally, the cytokine inhibitor, IL13, was elevated first in toddlers (p = 0.006) and again in young adults (p = 0.053). While the mean expression of interleukin-1 receptor antagonist (IL1RN) was highest in toddlers, this increase was not statistically significant. The fluctuations in cytokine expression reported here support a role for increases in specific cytokines at two different stages of human cortical development. The first is during the toddler/preschool period (IL1B, IL18, and IL13), and the other occurs at adolescence/young adult maturation (IL6, TNF and IL13).
除了在免疫细胞通讯中的传统作用外,细胞因子还调节大脑发育。已知细胞因子会影响神经细胞的生成、分化、成熟和存活。然而,大多数关于细胞因子在大脑发育中的作用的研究都是在啮齿动物中进行的,或者专注于产前事件。在这里,我们研究了关键细胞因子和细胞因子受体的 mRNA 和蛋白水平如何在人类前额叶皮层的出生后发育过程中发生变化。我们发现,研究中调查的大多数细胞因子转录本(IL1B、IL18、IL6、TNF、IL13)在出生时最低,并在 1.5 至 5 岁之间增加。5 岁后,转录模式朝着两个方向之一进行:青少年和年轻人的表达减少(IL1B,p=0.002;IL18,p=0.004)或随着成熟而增加表达,特别是在青少年(IL6,p=0.004;TNF,p=0.002;IL13,p<0.001)。相比之下,细胞因子蛋白在 3 岁左右达到峰值后趋于升高(IL1B,p=0.012;IL18,p=0.026;IL6,p=0.039;TNF,p<0.001),其中 TNF 蛋白在青少年中最高。细胞因子受体转录本的 mRNA 分析发现,细胞因子的早期发育增加与它们的配体结合受体亚基的增加相平行,例如 IL1R1(p=0.033)和 IL6R(p<0.001)转录本。相反,细胞因子受体相关信号亚基 IL1RAP 和 IL6ST 在年龄组之间没有明显变化。在两种 TNF 受体中,“促死亡”TNFRSF1A 和“促存活”TNFRSF1B,只有 TNFRSF1B 显著变化(p=0.028),首先在幼儿中增加,然后在年轻人中再次增加。最后,细胞因子抑制剂 IL13 首先在幼儿中升高(p=0.006),然后在年轻人中再次升高(p=0.053)。虽然白细胞介素-1 受体拮抗剂(IL1RN)的平均表达在幼儿中最高,但这种增加没有统计学意义。这里报道的细胞因子表达波动支持特定细胞因子在人类皮质发育的两个不同阶段增加的作用。第一个是在幼儿/学龄前期间(IL1B、IL18 和 IL13),另一个发生在青少年/成年成熟期间(IL6、TNF 和 IL13)。