Immune-endocrine interactions in endometriosis

review OA: bronze public-domain-us
AI-generated summary by claude@2026-06, 2026-06-13

This study examined how immune-endocrine interactions contribute to the development of endometriosis, a disease characterized by endometrial tissue outside the uterus and altered responses to sex steroids.

One-sentence paraphrase of the abstract; not a substitute for reading it. No clinical advice. How this works

AI-generated deep summary by claude@2026-06, 2026-06-13 · read from full text

This paper is a review focusing on how integrin receptors and extracellular matrix (ECM) interactions regulate cellular programs in the endocrine pancreas, particularly in pancreatic tissue morphogenesis and the survival/function of islet cells. It discusses the anti-apoptotic roles of integrins and how their signaling pathways affect islet development, survival, and function, with attention to how ECM-integrin relationships relate to islet-based therapies such as transplantation and pancreatic tissue engineering. The authors do not present original experimental data, and the summary is limited to what has been described in prior endocrine pancreas research and therapeutic contexts. This paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

Read from the paper's body, not the abstract. Not a substitute for reading the paper. No clinical advice. How this works

Abstract

Endocrine and immune systems are among the most essential regulators of endometrial physiology, and immune-endocrine interactions are likely to be involved in the pathogenesis of endometriosis. Endometriosis is an inflammatory, estrogen-dependent disease defined by the presence of viable endometrial tissue outside the uterine cavity. Impaired immune response that results in inadequate removal of refluxed menstrual debris has been proposed as a possible causative factor in the development of endometriosis. Moreover, decrease in spontaneous apoptosis of endometrium is the other theory proposed for the development of endometriosis. Endometriotic tissues respond to sex steroids aberrantly and behave differently compared to endometrium in addition to their ability to produce local estrogen. The effects of estrogen on distinct intracellular signaling pathways including MAPK, PI3K/AKT and NF-kappa B may take a role in enhanced endometrial cell survival, altered immune response, and differential cytokine and chemokine expression in endometriosis. Better understanding of immune-endocrine interactions will set the stage for effective immune-targeted therapies not only for endometriosis but also for other endometrial diseases such as adenomyosis, recurrent reproductive failure and implantation-related infertility.
Full text 1,499 characters · extracted from oa-doi-fallback · click to expand
Frontiers in Bioscience-Scholar (FBS) is published by IMR Press from Volume 13 Issue 1 (2021). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on imrpress.com as a courtesy and upon agreement with Frontiers in Bioscience. Integrins and extracellular matrices in pancreatic tissue engineering 1 Childrens' Health Research Institute, University of Western Ontario, London, ON, Canada 2 Department of Pathology, University of Western Ontario, London, ON, Canada 3 Physiology and Pharmacology, University of Western Ontario, London, ON, Canada 4 Medicine, University of Western Ontario, London, ON, Canada *Author to whom correspondence should be addressed. Abstract The role of integrin receptors in regulating numerous cellular programs have been well studied in the endocrine pancreas. These adhesion receptors and their interactions with the extracellular matrix (ECM) are important determinants of islet cell biology as they influence the development, survival and function of the islets of Langerhans. In this review, we will discuss the profound role of integrin-ECM relationships in controlling pancreatic tissue morphogenesis and the anti-apoptotic properties that these receptors confer through their dynamic and unique signaling pathways. Relationships between the ECM-integrin receptors will also be discussed in light of islet-based therapies including transplantation procedures and pancreatic tissue engineering initiatives.

Text is read by the "Ask this paper" AI Q&A widget below. Extraction quality varies by source — PMC NXML preserves structure cleanly, OA-HTML may include some navigation residue, and OA-PDF can have broken hyphenation. The publisher copy (via DOI) is the canonical version.

My notes (saved in your browser only)

Ask this paper AI returns verbatim quotes from the full text · source: oa-doi-fallback

Answers must be backed by verbatim quotes from this paper's full text. Hallucinated quotes are dropped automatically; if no verbatim passage answers the question, we say so. How this works

Condition tags

endometriosisadenomyosisinfertility

MeSH descriptors

Apoptosis Endometriosis Estrogens Immunity, Cellular Immunity, Humoral Immunologic Surveillance Signal Transduction Apoptosis Endometriosis Estrogens Estrogens Female Humans Immunity, Cellular Immunity, Humoral Immunologic Surveillance Killer Cells, Natural Killer Cells, Natural Macrophages Macrophages

Citation neighborhood (no data yet)

We don't have any in-corpus citations linked to this paper yet. The paper's references may be in our DB but unresolved to ``paper_id`` (resolution happens at ingest when the cited DOI matches a row we already have). Run the cross-source citation reconcile pass to retry.

Source provenance

europepmc
last seen: 2026-06-22T06:15:23.361955+00:00
pubmed
last seen: 2026-05-13T22:14:05.573375+00:00
unpaywall
last seen: 2026-05-14T19:30:52.867331+00:00
License: public-domain-us · commercial use OK · attribution required
Courtesy of the U.S. National Library of Medicine