Expression and Subcellular Localization of Endocannabinoid System in Primary Interstitial Glandular Cells In Situ of Mice Ovary

Authors

  • Anussara Kamnate Department of Anatomy, Faculty of Medicine, Princess of Naradhiwas University, Narathiwat 96000, Thailand

DOI:

https://doi.org/10.48048/tis.2022.6231

Keywords:

CB1, DAGL-α, Interstitial glandular cell, Ovary, Mice

Abstract

Endocannabinoid synthesizing 2-AG and cannabinoid receptors have been reported in some organ of reproductive system and in oocyte of ovary, but little is known about the expression and subcellular localization of CB1 and DAGL-α in interstitial gland tissue of mouse ovary. The aim of this study was to explain the differential distribution of endocannabinoid system in interstitial glandular cell of mouse ovary. The CB1 and DAGL-α-immunoreactivities were detected within cells, which are consisted of smaller mitochondria with non-tubular cristae and fewer lipid droplets within the interstitial glands. Their immunoreactivities were localized in association with small vesicle clustering dispersed throughout the cytoplasm. The identity of the immunoreactive cells within interstitial glands were showed a possibility of co-existence of CB1 and DAGL-α in steroidogenic cells and autocrine or paracrine exertion of eCB signaling as well as involvement of eCB signaling in regulation of cell differentiation were discussed.

HIGHLIGHTS

  • 2-arachidonoyl glycerol (2-AG, endocannabinoid)-synthesizing enzyme (DAGL-α) and its receptor CB1 localize to primary interstitial glandular cells of mice
  • The first time of study for DAGL isozymes a co-localize with CB1 in interstitial glandular cells by Immuno-DAB-electron-microscopy. The new knowledge represents DAGL isozymes a and CB1 locate in the intracellular vesicles. This suggests that 2-AG by DAGL-α and CB1 receptor had co-existence its function through paracrine/autocrine released, as already known in oocyte, neurons and some other cells
  • The distribution of DAGL isozymes a and CB1 in the interstitial gland tissues suggests that eCBs signaling molecules may be plays unique functions in steroidogenesis


GRAPHICAL ABSTRACT

Downloads

Download data is not yet available.

Metrics

Metrics Loading ...

References

OMH Habayeb, AH Taylor, MD Evans, MS Cooke, DJ Taylor, SC Bell and JC Konje. Plasma levels of the endocannabinoid anandamide in women a potential role in pregnancy maintenance and labor? J. Clin. Endocrinol. Metab. 2004; 89, 5482-7.

MR El-Talatini, AH Taylor, JC Elson, L Brown, AC Davidson and JC Konje. Localization and function of the endocannabinoid system in the human ovary. PLoS One 2009; 4, e4579.

N Battista, MD Tommaso, M Bari and M Maccarrone. The endocannabinoid system: An overview. Front. Behav. Neurosci. 2012; 6, 9.

T Ayakannu, AH Taylor, TH Marczylo, JM Willets and JC Konje. The endocannabinoid system and sex steroid hormone dependent cancers. Int. J. Endocrinol. 2013; 2013, 259676.

M Kano, T Ohno-Shosaku, Y Hashimotodani, M Uchigashima and M Watanabe. Endocannabinoid-mediated control of synaptic transmission. Physiol. Rev. 2009; 89, 309-80.

S Aquila, C Guido, A Santoro, I Perrotta, C Laezza, M Bifulco and A Sebastiano. Human sperm anatomy: Ultrastructural localization of the cannabinoid1 receptor and a potential role of anandamide in sperm survival and acrosome reaction. Anat. Rec. (Hoboken) 2010; 293, 298-309.

E Hebert-Chatelain, L Reguero, N Puente, B Lutz, F Chaouloff, R Rossignol, PV Piazza, G Benard, Pe Grandes and G Marsicano. Cannabinoid control of brain bioenergetics: Exploring the subcellular localization of the CB1 receptor. Mol. Metab. 2014; 3, 495-504.

E Agirregoitia, I Ibarra-Lecue, L Totorikaguena, R Mendoza, A Expósito, R Matorras, L Urigüen and N Agirregoitia. Dynamics of expression and localization of the cannabinoid system in granulosa cells during oocyte nuclear maturation. Fertil. Steril. 2015; 104, 753-60.

N Battista, M Bari and M Maccarrone. Endocannabinoids and reproductive events in health and disease. Handb. Exp. Pharmacol. 2015; 231, 341-65.

AP López-Cardona, MJ Sánchez-Calabuig, P Beltran-Breña, N Agirregoitia, D Rizos, E Agirregoitia, D Rizos, E Agirregoitia and A Gutierrez-Adán. Exocannabinoids effect on in vitro bovine oocyte maturation via activation of AKT and ERK1/2. Reproduction 2016; 152, 603-12.

S Cecconi, G Rossi, S Oddi, VD Nisio and M Maccarrone. Role of major endocannabinoid binding receptors during mouse oocyte maturation. Int. J. Mol. Sci. 2019; 20, 2866.

A Kamnate, J Sirisin, Y Polsan, S Chomphoo, M Watanabe, H Kondo and W Hipkaeo. In situ localization of diacylglycerol lipase α and β producing an endocannabinoid 2-arachidonoylglycerol and of cannabinoid receptor 1 in the primary oocytes of postnatal mice. J. Anat. 2021; 238, 1330-40.

W Mobius and G Posthuma. Sugar and ice: Immunoelectron microscopy using cryosections according to the Tokuyasu method. Tiss Cell. 2019; 57, 90-102.

Y Fukudome, T Ohno-Shosaku, M Matsui, Y Omori, M Fukaya, H Tsubokawa, MM Taketo, M Watanabe, T Manabe and M Kano. Two distinct classes of muscarinic action on hippocampal inhibitory synapses: M2 mediated direct suppression and M1/M3 mediated indirect suppression through endocannabinoid signaling. Eur. J. Neurosci. 2004; 19, 2682-92.

T Yoshida, M Fukaya, M Uchigashima, E Miura, H Kamiya, M Kano and M Watanabe. Localization of diacylglycerol lipase-α around postsynaptic spine suggests close proximity between production site of an endocannabinoid, 2-arachidonoyl-glycerol, and presynaptic cannabinoid CB1 receptor. J. Neurosci. 2006; 26, 4740-51.

M Uchigashima, M Narushima, M Fukaya, I Katona, M Kano and M Watanabe. Subcellular arrangement of molecules for 2-arachidonoyl-glycerol-mediated retrograde signaling and its physiological contribution to synaptic modulation in the striatum. J. Neurosci. 2007; 27, 3663-76.

W Thoungseabyoun, A Tachow, S Pakkarato, A Rawangwong, S Krongyut, W Sakaew, Hisatake Kondo and W Hipkaeo. Immunohistochemical localization of cannabinoid receptor 1 (CB1) in the submandibular gland of mice under normal conditions and when stimulated by isoproterenol or carbachol. Arch. Oral Biol. 2017; 81, 160-6.

SS Guraya. Recent advances in the morphology, histochemistry, biochemistry, and physiology of interstitial gland cells of mammalian ovary. Int. Rev. Cytol. 1978; 55, 171-245.

WJ Shen, S Azhar and FB Kraemer. Lipid droplets and steroidogenic cells. Exp. Cell Res. 2016; 340, 209-14.

I Galve-Roperh, V Chiurchiù, J Díaz-Alonso, M Bari, M Guzmán and M Maccarrone. Cannabinoid receptor signaling in progenitor/stem cell proliferation and differentiation. Prog. Lipid. Res. 2013; 52, 633-50.

M Garcia-Arencibia, E Molina-Holgado and F Molina-Holgado. Effect of endocannabinoid signalling on cell fate: life, death, differentiation and proliferation of brain cells. Br. J. Pharmacol. 2019; 176, 1361-9.

Downloads

Published

2022-10-11

How to Cite

Kamnate, A. . (2022). Expression and Subcellular Localization of Endocannabinoid System in Primary Interstitial Glandular Cells In Situ of Mice Ovary. Trends in Sciences, 19(20), 6231. https://doi.org/10.48048/tis.2022.6231