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Expression of Nerve Injury-Induced Protein1 (Ninj1) in Endometriosis.

AbstractOBJECTIVE:
The aim of this study was to clarify the expression of Ninj1 in endometriosis and adenomyosis lesions, and its inductive factor in human endometriotic stromal cells (ESCs).
BACKGROUND:
Nerve injury-induced protein 1 (Ninj1) is a molecule originally identified in dorsal root ganglion neurons and Schwann cells after nerve injury and promotes neurite outgrowth. The aim of this study was to clarify the expression of Ninj1 in endometriosis and adenomyosis lesions, and its inductive factor in human endometriotic stromal cells (ESCs).
MATERIALS AND METHODS:
Tissues were obtained with consent from patients diagnosed with ovarian endometrioma (n = 15 in total), peritoneal endometriosis (n = 5), adenomyosis (n = 5), and other gynecological disorders (n = 5, control) during surgery. Immunohistochemistry was conducted in order to detect Ninj1 protein expression in the lesion of endometriosis, adenomyosis, and eutopic endometrium. Nerve fibers in the ovarian endometrioma were detected by positive staining of PGP-9.5. To evaluate the effects of IL-1β on Ninj1 gene expression in endometriosis, ESCs isolated from ovarian endometrioma (n = 5) were treated with IL-1β (5 ng/mL) for 3 or 6 hours. Messenger RNA (mRNA) expression for Ninj1 was examined using quantitative RT-PCR.
RESULTS:
The Ninj1 protein was expressed by ovarian endometrioma, peritoneal endometriotic, and adenomyotic tissue. Nerve fibers were found in the areas of positive staining for Ninj1 in ovarian endometrioma. IL-1β, an indicator of inflammation in endometriosis, significantly increased Ninj1 mRNA expression by ESC.
CONCLUSION:
Our study demonstrates that Ninj1 is expressed in endometriosis and adenomyosis and is induced by the inflammatory stimuli. Given the neurogenetic property of Ninj1, our results imply that Ninj1, induced by inflammation in endometriosis lesion, may contribute to the pathogenesis of pain symptoms characteristic of endometriosis.
AuthorsMariko Miyashita, Kaori Koga, Arisa Takeuchi, Tomoko Makabe, Ayumi Taguchi, Yoko Urata, Gentaro Izumi, Masashi Takamura, Miyuki Harada, Tetsuya Hirata, Yasushi Hirota, Osamu Wada-Hiraike, Osamu Yoshino, Tomoyuki Fujii, Yutaka Osuga
JournalReproductive sciences (Thousand Oaks, Calif.) (Reprod Sci) Vol. 26 Issue 8 Pg. 1105-1110 (08 2019) ISSN: 1933-7205 [Electronic] United States
PMID30326781 (Publication Type: Journal Article)
Chemical References
  • Cell Adhesion Molecules, Neuronal
  • Interleukin-1beta
  • NINJ1 protein, human
  • Nerve Growth Factors
Topics
  • Adenomyosis (metabolism)
  • Cell Adhesion Molecules, Neuronal (metabolism)
  • Endometriosis (metabolism)
  • Endometrium (drug effects, metabolism)
  • Female
  • Gene Expression Regulation (drug effects)
  • Humans
  • Immunohistochemistry
  • Inflammation (metabolism)
  • Interleukin-1beta (pharmacology)
  • Nerve Growth Factors (metabolism)
  • Ovarian Diseases (metabolism)
  • Peritoneal Diseases (metabolism)
  • Stromal Cells (drug effects, metabolism)

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