Mohri Ikuko, Taniike Masako, Taniguchi Hidetoshi, Kanekiyo Takahisa, Aritake Kosuke, Inui Takashi, Fukumoto Noriko, Eguchi Naomi, Kushi Atsuko, Sasai Hitoshi, Kanaoka Yoshihide, Ozono Keiichi, Narumiya Shuh, Suzuki Kinuko, Urade Yoshihiro
Department of Developmental Medicine (Pediatrics), Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan.
J Neurosci. 2006 Apr 19;26(16):4383-93. doi: 10.1523/JNEUROSCI.4531-05.2006.
Prostaglandin (PG) D2 is well known as a mediator of inflammation. Hematopoietic PGD synthase (HPGDS) is responsible for the production of PGD2 involved in inflammatory responses. Microglial activation and astrogliosis are commonly observed during neuroinflammation, including that which occurs during demyelination. Using the genetic demyelination mouse twitcher, a model of human Krabbe's disease, we discovered that activated microglia expressed HPGDS and activated astrocytes expressed the DP1 receptor for PGD2 in the brain of these mice. Cultured microglia actively produced PGD2 by the action of HPGDS. Cultured astrocytes expressed two types of PGD2 receptor, DP1 and DP2, and showed enhanced GFAP production after stimulation of either receptor with its respective agonist. These results suggest that PGD2 plays an important role in microglia/astrocyte interaction. We demonstrated that the blockade of the HPGDS/PGD2/DP signaling pathway using HPGDS- or DP1-null twitcher mice, and twitcher mice treated with an HPGDS inhibitor, HQL-79 (4-benzhydryloxy-1-[3-(1H-tetrazol-5-yl)-propyl]piperidine), resulted in remarkable suppression of astrogliosis and demyelination, as well as a reduction in twitching and spasticity. Furthermore, we found that the degree of oligodendroglial apoptosis was also reduced in HPGDS-null and HQL-79-treated twitcher mice. These results suggest that PGD2 is the key neuroinflammatory molecule that heightens the pathological response to demyelination in twitcher mice.
前列腺素(PG)D2是一种众所周知的炎症介质。造血PGD合酶(HPGDS)负责产生参与炎症反应的PGD2。在神经炎症(包括脱髓鞘过程中发生的神经炎症)期间,通常会观察到小胶质细胞活化和星形胶质细胞增生。利用遗传性脱髓鞘小鼠“颤抖鼠”(一种人类克拉伯病模型),我们发现活化的小胶质细胞在这些小鼠大脑中表达HPGDS,而活化的星形胶质细胞表达PGD2的DP1受体。培养的小胶质细胞通过HPGDS的作用积极产生PGD2。培养的星形胶质细胞表达两种类型的PGD2受体,即DP1和DP2,在用各自的激动剂刺激任一受体后,GFAP产生增加。这些结果表明,PGD2在小胶质细胞/星形胶质细胞相互作用中起重要作用。我们证明,使用HPGDS基因敲除或DP1基因敲除的“颤抖鼠”以及用HPGDS抑制剂HQL-79(4-二苯甲氧基-1-[3-(1H-四氮唑-5-基)-丙基]哌啶)处理的“颤抖鼠”阻断HPGDS/PGD2/DP信号通路,可显著抑制星形胶质细胞增生和脱髓鞘,以及减少抽搐和痉挛。此外,我们发现HPGDS基因敲除和HQL-79处理的“颤抖鼠”中少突胶质细胞凋亡程度也降低。这些结果表明,PGD2是加剧“颤抖鼠”对脱髓鞘病理反应的关键神经炎症分子。