Over-expressed KRT8 in the cytotrophoblast shell promotes the development of preeclampsia

Abstract

Preeclampsia is a "placenta-derived disorder" characterized disease, which remains a major unaddressed public health problem. The differentiation and development of cytotrophoblasts and extravillous trophoblasts are two crucial processes, which are tightly regulated. And any abnormal regulation can lead to the occurrence of pregnancy-related diseases such as preeclampsia. In this article, we performed Spatial transcriptomics on tissues of PE and Normal, and found a large amount of extravillous trophoblasts (EVTs) were accumulated in the cluster 8 (cytotrophoblast shell) of PE_decidua, and Trajectory analysis revealed KRT8 was over-expressed in the cytotrophoblast shell of PE_decidua. The accumulation of EVTs caused by the increase of KRT8 promotes the development of preeclampsia.

Competing Interest Statement

The authors have declared no competing interest.

Clinical Trial

not applicable

Funding Statement

Fund of Hubei Province Chutian Talent Program; Major science and technology projects in Hubei Province?No.2022AC005?; Hubei Provincial Department of Science and Technology (No. 2022CFB561)

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

The study was approved by the Ethics committee of Maternal and Child Health Hospital of Hubei Province (2021XM049).

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

Yes

I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

Data Availability

The datasets used and analyzed during the current study are available from the corresponding author on reasonable request

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