Electron Microscopy Unit, Department of Anatomy, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
Department of Anatomy, Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
J Anat. 2021 Jun;238(6):1330-1340. doi: 10.1111/joa.13392. Epub 2021 Jan 4.
In order to understand the mechanism of the endocannabinoid (eCB) signal, which has so far been shown to work in oocyte genesis and maturation, it is critical to clarify detailed localization of the eCB synthesizing enzyme molecules as well as receptors for eCBs in oocytes in the ovary in situ. For this purpose, diacylglycerol lipase (DGL) α and β are involved in the synthesis of an eCB 2-arachidonoylglycerol (2-AG). DGLα/β and the cannabinoid receptor 1 (CB1) for 2-AG were shown to be localized to the primary oocytes of postnatal mice using immuno-light and electron microscopy. It was found that two types of localization existed: first, immunoreactivities for DGLα and β were weakly detected throughout the ooplasm in light microscopy for which the intracellular membranes of vesicles forming tiny scattered aggregates were responsible. Secondly, DGLβ-immunoreactivity was distinctly confined to the nuage of Balbiani bodies and small nuage-derivative structures; both amorphous materials and membranes of vesicles were responsible for their localization. On the other hand, the weak immunoreactivity for CB1 was localized in a pattern similar to the first one for DGLs, but not found in a pattern for the Balbiani nuage. Two routes of functional exertion of 2-AG synthesized by DGLs were suggested from the two types of localization: one was that the eCB synthesized at all the sites of DGLs is released from the oocytes and exerts paracrine or autocrine effects on adjacent intra-ovarian cells as well as the oocytes themselves. The other was that the eCB synthesized within the nuage was involved in the modulation of the posttranscriptional processing of oocytes. Owing to the failure in the detection of CB1 in the Balbiani nuage, however, the validity of the latter possibility remains to be elucidated.
为了了解内源性大麻素(eCB)信号的作用机制,目前已经表明该信号在卵母细胞发生和成熟中起作用,因此,必须明确在卵巢原位中卵母细胞内合成 eCB 的酶分子以及 eCB 受体的详细定位。为此,二酰基甘油脂肪酶(DGL)α和β参与 eCB 2-花生四烯酰甘油(2-AG)的合成。使用免疫荧光和电子显微镜,已经证明 DGLα/β和 2-AG 的大麻素受体 1(CB1)定位于新生小鼠的初级卵母细胞。发现存在两种类型的定位:首先,在光镜下,DGLα和β的免疫反应性在整个卵质中被弱检测到,这是由于形成微小分散聚集体的囊泡的细胞内膜所致。其次,DGLβ免疫反应性明显局限于巴尔比安尼体的核质和小核质衍生结构;无定形物质和囊泡的膜都负责其定位。另一方面,CB1 的弱免疫反应性定位于与 DGLs 相似的模式,但不在巴尔比安尼核质的模式中。从这两种定位方式推测,DGL 合成的 2-AG 有两种功能发挥途径:一种是在 DGLs 的所有部位合成的 eCB 从卵母细胞中释放出来,并对邻近的卵巢内细胞以及卵母细胞本身发挥旁分泌或自分泌作用。另一种是在核质内合成的 eCB 参与卵母细胞转录后加工的调节。然而,由于在巴尔比安尼核质中未能检测到 CB1,因此后一种可能性的有效性仍有待阐明。