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KLF10 Mediated Epigenetic Dysregulation of Epithelial CD40/CD154 Promotes Endometriosis

Endometriosis is a highly prevalent, chronic, heterogeneous, fibro-inflammatory disease that remains recalcitrant to conventional therapy. We previously showed that loss of KLF11, a transcription factor implicated in uterine disease, results in progression of endometriosis. Despite extensive homolog...

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Autores principales: Delaney, Abigail A., Khan, Zaraq, Zheng, Ye, Correa, Luiz F., Zanfagnin, Valentina, Shenoy, Chandra C., Schoolmeester, John K., Saadalla, Abdulrahman M., El-Nashar, Sherif, Famuyide, Abimbola O., Subramaniam, Malayannan, Hawse, John R., Khazaie, Khashayarsha, Daftary, Gaurang S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for the Study of Reproduction, Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5333936/
https://www.ncbi.nlm.nih.gov/pubmed/27488034
http://dx.doi.org/10.1095/biolreprod.116.140764
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author Delaney, Abigail A.
Khan, Zaraq
Zheng, Ye
Correa, Luiz F.
Zanfagnin, Valentina
Shenoy, Chandra C.
Schoolmeester, John K.
Saadalla, Abdulrahman M.
El-Nashar, Sherif
Famuyide, Abimbola O.
Subramaniam, Malayannan
Hawse, John R.
Khazaie, Khashayarsha
Daftary, Gaurang S.
author_facet Delaney, Abigail A.
Khan, Zaraq
Zheng, Ye
Correa, Luiz F.
Zanfagnin, Valentina
Shenoy, Chandra C.
Schoolmeester, John K.
Saadalla, Abdulrahman M.
El-Nashar, Sherif
Famuyide, Abimbola O.
Subramaniam, Malayannan
Hawse, John R.
Khazaie, Khashayarsha
Daftary, Gaurang S.
author_sort Delaney, Abigail A.
collection PubMed
description Endometriosis is a highly prevalent, chronic, heterogeneous, fibro-inflammatory disease that remains recalcitrant to conventional therapy. We previously showed that loss of KLF11, a transcription factor implicated in uterine disease, results in progression of endometriosis. Despite extensive homology, co-expression, and human disease association, loss of the paralog Klf10 causes a unique inflammatory, cystic endometriosis phenotype in contrast to fibrotic progression seen with loss of Klf11. We identify here for the first time a novel role for KLF10 in endometriosis. In an animal endometriosis model, unlike wild-type controls, Klf10(−/−) animals developed cystic lesions with massive immune infiltrate and minimal peri-lesional fibrosis. The Klf10(−/−) disease progression phenotype also contrasted with prolific fibrosis and minimal immune cell infiltration seen in Klf11(−/−) animals. We further found that lesion genotype rather than that of the host determined each unique disease progression phenotype. Mechanistically, KLF10 regulated CD40/CD154-mediated immune pathways. Both inflammatory as well as fibrotic phenotypes are the commonest clinical manifestations in chronic fibro-inflammatory diseases such as endometriosis. The complementary, paralogous Klf10 and Klf11 models therefore offer novel insights into the mechanisms of inflammation and fibrosis in a disease-relevant context. Our data suggests that divergence in underlying gene dysregulation critically determines disease-phenotype predominance rather than the conventional paradigm of inflammation being precedent to fibrotic scarring. Heterogeneity in clinical progression and treatment response are thus likely from disparate gene regulation profiles. Characterization of disease phenotype-associated gene dysregulation offers novel approaches for developing targeted, individualized therapy for recurrent and recalcitrant chronic disease.
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spelling pubmed-53339362017-09-01 KLF10 Mediated Epigenetic Dysregulation of Epithelial CD40/CD154 Promotes Endometriosis Delaney, Abigail A. Khan, Zaraq Zheng, Ye Correa, Luiz F. Zanfagnin, Valentina Shenoy, Chandra C. Schoolmeester, John K. Saadalla, Abdulrahman M. El-Nashar, Sherif Famuyide, Abimbola O. Subramaniam, Malayannan Hawse, John R. Khazaie, Khashayarsha Daftary, Gaurang S. Biol Reprod Articles Endometriosis is a highly prevalent, chronic, heterogeneous, fibro-inflammatory disease that remains recalcitrant to conventional therapy. We previously showed that loss of KLF11, a transcription factor implicated in uterine disease, results in progression of endometriosis. Despite extensive homology, co-expression, and human disease association, loss of the paralog Klf10 causes a unique inflammatory, cystic endometriosis phenotype in contrast to fibrotic progression seen with loss of Klf11. We identify here for the first time a novel role for KLF10 in endometriosis. In an animal endometriosis model, unlike wild-type controls, Klf10(−/−) animals developed cystic lesions with massive immune infiltrate and minimal peri-lesional fibrosis. The Klf10(−/−) disease progression phenotype also contrasted with prolific fibrosis and minimal immune cell infiltration seen in Klf11(−/−) animals. We further found that lesion genotype rather than that of the host determined each unique disease progression phenotype. Mechanistically, KLF10 regulated CD40/CD154-mediated immune pathways. Both inflammatory as well as fibrotic phenotypes are the commonest clinical manifestations in chronic fibro-inflammatory diseases such as endometriosis. The complementary, paralogous Klf10 and Klf11 models therefore offer novel insights into the mechanisms of inflammation and fibrosis in a disease-relevant context. Our data suggests that divergence in underlying gene dysregulation critically determines disease-phenotype predominance rather than the conventional paradigm of inflammation being precedent to fibrotic scarring. Heterogeneity in clinical progression and treatment response are thus likely from disparate gene regulation profiles. Characterization of disease phenotype-associated gene dysregulation offers novel approaches for developing targeted, individualized therapy for recurrent and recalcitrant chronic disease. Society for the Study of Reproduction, Inc. 2016-08-03 2016-09 /pmc/articles/PMC5333936/ /pubmed/27488034 http://dx.doi.org/10.1095/biolreprod.116.140764 Text en © 2016 by the Society for the Study of Reproduction, Inc. http://creativecommons.org/licenses/by-nc/4.0/ This article is available under a Creative Commons License 4.0 (Attribution-Non-Commercial), as described at http://creativecommons.org/licenses/by-nc/4.0
spellingShingle Articles
Delaney, Abigail A.
Khan, Zaraq
Zheng, Ye
Correa, Luiz F.
Zanfagnin, Valentina
Shenoy, Chandra C.
Schoolmeester, John K.
Saadalla, Abdulrahman M.
El-Nashar, Sherif
Famuyide, Abimbola O.
Subramaniam, Malayannan
Hawse, John R.
Khazaie, Khashayarsha
Daftary, Gaurang S.
KLF10 Mediated Epigenetic Dysregulation of Epithelial CD40/CD154 Promotes Endometriosis
title KLF10 Mediated Epigenetic Dysregulation of Epithelial CD40/CD154 Promotes Endometriosis
title_full KLF10 Mediated Epigenetic Dysregulation of Epithelial CD40/CD154 Promotes Endometriosis
title_fullStr KLF10 Mediated Epigenetic Dysregulation of Epithelial CD40/CD154 Promotes Endometriosis
title_full_unstemmed KLF10 Mediated Epigenetic Dysregulation of Epithelial CD40/CD154 Promotes Endometriosis
title_short KLF10 Mediated Epigenetic Dysregulation of Epithelial CD40/CD154 Promotes Endometriosis
title_sort klf10 mediated epigenetic dysregulation of epithelial cd40/cd154 promotes endometriosis
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5333936/
https://www.ncbi.nlm.nih.gov/pubmed/27488034
http://dx.doi.org/10.1095/biolreprod.116.140764
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