Defining cardiac cell populations and relative cellular composition of the early fetal human heart
Defining cardiac cell populations and relative cellular composition of the early fetal human heart
While the adult human heart is primarily composed of cardiomyocytes, fibroblasts, endothelial and smooth muscle cells, the cellular composition during early development remains largely unknown. Reliable identification of fetal cardiac cell types using protein markers is critical to understand cardiac development and delineate the cellular composition of the developing human heart. This is the first study to use immunohistochemistry (IHC), flow cytometry and RT-PCR analyses to investigate the expression and specificity of commonly used cardiac cell markers in the early human fetal heart (8–12 post-conception weeks). The expression of previously reported protein markers for the detection of cardiomyocytes (Myosin Heavy Chain (MHC) and cardiac troponin I (cTnI), fibroblasts (DDR2, THY1, Vimentin), endothelial cells (CD31) and smooth muscle cells (α-SMA) were assessed. Two distinct populations of cTnI positive cells were identified through flow cytometry, with MHC positive cardiomyocytes showing high cTnI expression (cTnI
High) while MHC negative non-myocytes showed lower cTnI expression (cTnI
Low). cTnI expression in non-myocytes was further confirmed by IHC and RT-PCR analyses, suggesting troponins are not cardiomyocyte-specific and may play distinct roles in non-muscle cells during early development. Vimentin (VIM) was expressed in cultured ventricular fibroblast populations and flow cytometry revealed VIM
High and VIM
Low cell populations in the fetal heart. MHC positive cardiomyocytes were VIM
Low whilst CD31 positive endothelial cells were VIM
High. Using markers investigated within this study, we characterised fetal human cardiac populations and estimate that 75–80% of fetal cardiac cells are cardiomyocytes and are MHC
+/cTnI
High/VIM
Low, whilst non-myocytes comprise 20–25% of total cells and are MHC
-/cTnI
Low/VIM
High, with CD31
+ endothelial cells comprising ~9% of this population. These findings show distinct differences from those reported for adult heart.
Dewing, Jennifer M.
868fbf01-7b6e-499f-abf9-47409278373f
Saunders, Vinay
0097e3f0-9e0f-4bcd-8b56-0d90201bd2f9
O’kelly, Ita
e640f28a-42f0-48a6-9ce2-cb5a85d08c66
Wilson, David I.
b859b9ee-173f-4613-98a5-79a7099f15ae
30 November 2022
Dewing, Jennifer M.
868fbf01-7b6e-499f-abf9-47409278373f
Saunders, Vinay
0097e3f0-9e0f-4bcd-8b56-0d90201bd2f9
O’kelly, Ita
e640f28a-42f0-48a6-9ce2-cb5a85d08c66
Wilson, David I.
b859b9ee-173f-4613-98a5-79a7099f15ae
Dewing, Jennifer M., Saunders, Vinay, O’kelly, Ita and Wilson, David I.
(2022)
Defining cardiac cell populations and relative cellular composition of the early fetal human heart.
PLoS ONE, 17 (11), [e0259477].
(doi:10.1371/journal.pone.0259477).
Abstract
While the adult human heart is primarily composed of cardiomyocytes, fibroblasts, endothelial and smooth muscle cells, the cellular composition during early development remains largely unknown. Reliable identification of fetal cardiac cell types using protein markers is critical to understand cardiac development and delineate the cellular composition of the developing human heart. This is the first study to use immunohistochemistry (IHC), flow cytometry and RT-PCR analyses to investigate the expression and specificity of commonly used cardiac cell markers in the early human fetal heart (8–12 post-conception weeks). The expression of previously reported protein markers for the detection of cardiomyocytes (Myosin Heavy Chain (MHC) and cardiac troponin I (cTnI), fibroblasts (DDR2, THY1, Vimentin), endothelial cells (CD31) and smooth muscle cells (α-SMA) were assessed. Two distinct populations of cTnI positive cells were identified through flow cytometry, with MHC positive cardiomyocytes showing high cTnI expression (cTnI
High) while MHC negative non-myocytes showed lower cTnI expression (cTnI
Low). cTnI expression in non-myocytes was further confirmed by IHC and RT-PCR analyses, suggesting troponins are not cardiomyocyte-specific and may play distinct roles in non-muscle cells during early development. Vimentin (VIM) was expressed in cultured ventricular fibroblast populations and flow cytometry revealed VIM
High and VIM
Low cell populations in the fetal heart. MHC positive cardiomyocytes were VIM
Low whilst CD31 positive endothelial cells were VIM
High. Using markers investigated within this study, we characterised fetal human cardiac populations and estimate that 75–80% of fetal cardiac cells are cardiomyocytes and are MHC
+/cTnI
High/VIM
Low, whilst non-myocytes comprise 20–25% of total cells and are MHC
-/cTnI
Low/VIM
High, with CD31
+ endothelial cells comprising ~9% of this population. These findings show distinct differences from those reported for adult heart.
Text
journal.pone.0259477
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Accepted/In Press date: 8 November 2022
Published date: 30 November 2022
Additional Information:
Copyright: © 2022 Dewing et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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Local EPrints ID: 473289
URI: http://eprints.soton.ac.uk/id/eprint/473289
ISSN: 1932-6203
PURE UUID: 0adee2f5-56d1-4559-b753-939214d5be29
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Date deposited: 13 Jan 2023 17:49
Last modified: 16 Mar 2024 23:32
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Contributors
Author:
Jennifer M. Dewing
Author:
Vinay Saunders
Author:
Ita O’kelly
Author:
David I. Wilson
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