The Non-pregnant and Pregnant Human Cervix : a Systematic Proteomic Analysis
© 2022. Society for Reproductive Investigation..
Appropriate timing of cervical remodeling (CR) is key to normal term parturition. To date, mechanisms behind normal and abnormal (premature or delayed) CR remain unclear. Recent studies show regional differences exist in human cervical tissue structure. While the entire cervix contains extracellular matrix (ECM), the internal os is highly cellular containing 50-60% cervical smooth muscle (CSM). The external os contains 10-20% CSM. Previously, we reported ECM rigidity and different ECM proteins influence CSM cell function, highlighting the importance of understanding not only how cervical cells orchestrate cervical ECM remodeling in pregnancy, but also how changes in specific ECM proteins can influence resident cellular function. To understand this dynamic process, we utilized a systematic proteomic approach to understand which soluble ECM and cellular proteins exist in the different regions of the human cervix and how the proteomic profiles change from the non-pregnant (NP) to the pregnant (PG) state. We found the human cervix proteome contains at least 4548 proteins and establish the types and relative abundance of cellular and soluble matrisome proteins found in the NP and PG human cervix. Further, we report the relative abundance of proteins involved with elastic fiber formation and ECM organization/degradation were significantly increased while proteins involved in RNA polymerase I/promoter opening, DNA methylation, senescence, immune system, and compliment activation were decreased in the PG compared to NP cervix. These findings establish an initial platform from which we can further comprehend how changes in the human cervix proteome results in normal and abnormal CR.
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2022 |
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| Erschienen: |
2022 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:29 |
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| Enthalten in: |
Reproductive sciences (Thousand Oaks, Calif.) - 29(2022), 5 vom: 09. Mai, Seite 1542-1559 |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Barnum, Carrie E [VerfasserIn] |
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| Links: |
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| Themen: |
Cervical remodeling |
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| Anmerkungen: |
Date Completed 14.04.2022 Date Revised 09.05.2022 published: Print-Electronic Citation Status MEDLINE |
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| doi: |
10.1007/s43032-022-00892-4 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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| PPN (Katalog-ID): |
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| 245 | 1 | 4 | |a The Non-pregnant and Pregnant Human Cervix |b a Systematic Proteomic Analysis |
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| 520 | |a Appropriate timing of cervical remodeling (CR) is key to normal term parturition. To date, mechanisms behind normal and abnormal (premature or delayed) CR remain unclear. Recent studies show regional differences exist in human cervical tissue structure. While the entire cervix contains extracellular matrix (ECM), the internal os is highly cellular containing 50-60% cervical smooth muscle (CSM). The external os contains 10-20% CSM. Previously, we reported ECM rigidity and different ECM proteins influence CSM cell function, highlighting the importance of understanding not only how cervical cells orchestrate cervical ECM remodeling in pregnancy, but also how changes in specific ECM proteins can influence resident cellular function. To understand this dynamic process, we utilized a systematic proteomic approach to understand which soluble ECM and cellular proteins exist in the different regions of the human cervix and how the proteomic profiles change from the non-pregnant (NP) to the pregnant (PG) state. We found the human cervix proteome contains at least 4548 proteins and establish the types and relative abundance of cellular and soluble matrisome proteins found in the NP and PG human cervix. Further, we report the relative abundance of proteins involved with elastic fiber formation and ECM organization/degradation were significantly increased while proteins involved in RNA polymerase I/promoter opening, DNA methylation, senescence, immune system, and compliment activation were decreased in the PG compared to NP cervix. These findings establish an initial platform from which we can further comprehend how changes in the human cervix proteome results in normal and abnormal CR | ||
| 650 | 4 | |a Journal Article | |
| 650 | 4 | |a Research Support, N.I.H., Extramural | |
| 650 | 4 | |a Research Support, Non-U.S. Gov't | |
| 650 | 4 | |a Cervical remodeling | |
| 650 | 4 | |a Cervix | |
| 650 | 4 | |a Extracellular matrix | |
| 650 | 4 | |a Pregnancy | |
| 650 | 4 | |a Proteins | |
| 650 | 4 | |a Proteomics | |
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| 700 | 1 | |a Shetye, Snehal S |e verfasserin |4 aut | |
| 700 | 1 | |a Fazelinia, Hossein |e verfasserin |4 aut | |
| 700 | 1 | |a Garcia, Benjamin A |e verfasserin |4 aut | |
| 700 | 1 | |a Fang, Shuyang |e verfasserin |4 aut | |
| 700 | 1 | |a Alzamora, Maria |e verfasserin |4 aut | |
| 700 | 1 | |a Li, Hongyu |e verfasserin |4 aut | |
| 700 | 1 | |a Brown, Lewis M |e verfasserin |4 aut | |
| 700 | 1 | |a Tang, Chuanning |e verfasserin |4 aut | |
| 700 | 1 | |a Myers, Kristin |e verfasserin |4 aut | |
| 700 | 1 | |a Wapner, Ronald |e verfasserin |4 aut | |
| 700 | 1 | |a Soslowsky, Louis J |e verfasserin |4 aut | |
| 700 | 1 | |a Vink, Joy Y |e verfasserin |4 aut | |
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