Literature DB >> 8384220

An aromatase-associated cytoplasmic inclusion, the "stigmoid body," in the rat brain: II. Ultrastructure (with a review of its history and nomenclature).

K Shinoda1, M Nagano, Y Osawa.   

Abstract

The ultrastructure of aromatase-associated "stigmoid (dot-like) structures," which were detected in a previous study using light-microscopic immunohistochemistry (Shinoda et al.: J. Comp. Neurol. 322:360-376, '92), were examined in the rat medial preoptic region, bed nucleus of the stria terminalis, medial amygdaloid nucleus, and arcuate nucleus by pre- and post-embedding marking with a polyclonal antibody against human placental antigen X-P2 (hPAX-P2) for immuno-electron microscopic analysis. The immunoreactive stigmoid structure was identified as a distinct, non-membrane-bounded cytoplasmic inclusion (approximately 1-3 microns in diameter), which has a granulo-fuzzy texture with moderate-to-low electron density in non-immunostained preparations. It consists of at least four distinct granular and three distinct fibrillo-tubular elements forming a granulo-fibrillar conglomerate. This type of inclusions was formally termed the "stigmoid body" under the electron microscope. The stigmoid body is composed of the outer granulo-fibrillar and inner hyaloplasmic compartments. The immunoreactivity for hPAX-P2 is mainly localized to the former, especially to the low density granulo-fuzzy materials associated with the fibrillo-tubular elements. Identification of the ultrastructure of stigmoid body clarified their prevalence not only in the limbic and hypothalamic regions, but also in sex-steroid-sensitive peripheral tissues (e.g., peripheral sensory ganglia, ovary, testis) by consulting earlier electron-microscopic studies. Reviewing the history and nomenclature of this inclusion body, we reorganized the terminology of related neuronal cytoplasmic inclusions, the terms of which have often been confused, and discussed its functional significance on the basis of the present and previously accumulated data. In conclusion, we emphasized the importance of the stigmoid bodies in the sex-steroid-sensitive neural system because of their large size, high frequency, specific distribution in brains and peripheral tissues, effects of sex-steroids, and immunological and histochemical characteristics of the antibody marking the inclusion. The stigmoid bodies may provide a subcellular site for sex-steroid metabolism in their target tissues and play a critical role in cytosolic modulation of their actions (e.g., by aromatization) prior to their receptor binding.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8384220     DOI: 10.1002/cne.903290102

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  12 in total

1.  Cellular and subcellular localization of PKMζ.

Authors:  A Iván Hernández; William C Oxberry; John F Crary; Suzanne S Mirra; Todd Charlton Sacktor
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2013-12-02       Impact factor: 6.237

2.  Immunohistochemical localization of huntingtin-associated protein 1 in endocrine system of the rat.

Authors:  Min Liao; Jianying Shen; Yinong Zhang; Shi-Hua Li; Xiao-Jiang Li; He Li
Journal:  J Histochem Cytochem       Date:  2005-08-08       Impact factor: 2.479

3.  DYRK1A regulates Hap1-Dcaf7/WDR68 binding with implication for delayed growth in Down syndrome.

Authors:  Jianxing Xiang; Su Yang; Ning Xin; Marta A Gaertig; Roger H Reeves; Shihua Li; Xiao-Jiang Li
Journal:  Proc Natl Acad Sci U S A       Date:  2017-01-30       Impact factor: 11.205

4.  Immunohistochemical expression and neurochemical phenotypes of huntingtin-associated protein 1 in the myenteric plexus of mouse gastrointestinal tract.

Authors:  Abu Md Mamun Tarif; Md Nabiul Islam; Mir Rubayet Jahan; Akie Yanai; Kanako Nozaki; Koh-Hei Masumoto; Koh Shinoda
Journal:  Cell Tissue Res       Date:  2021-10-19       Impact factor: 5.249

5.  Microtubule-dependent formation of the stigmoid body as a cytoplasmic inclusion distinct from pathological aggresomes.

Authors:  Ryutaro Fujinaga; Yukio Takeshita; Kanako Uozumi; Akie Yanai; Kazuhiro Yoshioka; Keiji Kokubu; Koh Shinoda
Journal:  Histochem Cell Biol       Date:  2009-07-04       Impact factor: 4.304

Review 6.  Huntingtin associated protein 1 and its functions.

Authors:  Linda Lin-yan Wu; Xin-Fu Zhou
Journal:  Cell Adh Migr       Date:  2009-01-26       Impact factor: 3.405

7.  The cellular and subcellular localization of huntingtin-associated protein 1 (HAP1): comparison with huntingtin in rat and human.

Authors:  C A Gutekunst; S H Li; H Yi; R J Ferrante; X J Li; S M Hersch
Journal:  J Neurosci       Date:  1998-10-01       Impact factor: 6.167

8.  Huntingtin-associated protein 1 interacts with Ahi1 to regulate cerebellar and brainstem development in mice.

Authors:  Guoqing Sheng; Xingshun Xu; Yung-Feng Lin; Chuan-En Wang; Juan Rong; Dongmei Cheng; Junmin Peng; Xiaoyan Jiang; Shi-Hua Li; Xiao-Jiang Li
Journal:  J Clin Invest       Date:  2008-08       Impact factor: 14.808

9.  Aromatase-immunoreactive cells are present in mouse brain areas that are known to express high levels of aromatase activity.

Authors:  A Foidart; N Harada; J Balthazart
Journal:  Cell Tissue Res       Date:  1995-06       Impact factor: 5.249

10.  Anti-human placental antigen complex X-P2 (hPAX-P2) anti-serum recognizes C-terminus of huntingtin-associated protein 1A common to 1B as a determinant marker for the stigmoid body.

Authors:  Ryutaro Fujinaga; Akie Yanai; Hirokazu Nakatsuka; Kumiko Yoshida; Yukio Takeshita; Kanako Uozumi; Changjiu Zhao; Kazuko Hirata; Keiji Kokubu; Mamoru Nagano; Koh Shinoda
Journal:  Histochem Cell Biol       Date:  2007-08-09       Impact factor: 4.304

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.