Proteomics of human postnatal lung epithelial, endothelial, mesenchymal, and immune cells

Mereena G. Ushakumary1, Song Feng1, Gautam Bandyopadhyay2, Heather Olson1, Karl K. Weitz1, Heidi L. Huyck2, Cory Poole2, Jeffrey M. Purkerson2, Soumyaroop Bhattacharya2, Cecilia Ljungberg3, Thomas J. Mariani2, Gail H. Deutsch4, Ravi Misra2, James P. Carson5, Joshua N. Adkins1, Charles Ansong1, Gloria Pryhuber2, Geremy Clair1
1Pacific Northwest National Laboratory, 2University of Rochester Medical Center, 3Baylor College of Medicine, 4University of Washington, 5University of Texas at Austin, *Corresponding author
Description The lung is a vital organ that undergoes extensive morphological and functional changes during postnatal development. To disambiguate how different cell populations contribute to organ development, we performed proteomic and transcriptomic analyses of four sorted cell populations from the lung of human subjects aged 0 to 8 years-old with a focus on early life. The cell populations analyzed included epithelial, endothelial, mesenchymal, and immune cells. Our results revealed distinct molecular signatures for each of the sorted cell populations that enable the description of molecular shifts occurring in these populations during post-natal development. We confirmed that the proteome of the different cell populations was distinct regardless of age and identified functions specific to each population. We identified a series of cell population protein markers, including those located at the cell surface, that show differential expression and distribution on RNA in situ hybridization and immunofluorescence imaging. We validated the spatial distribution of AT1 and endothelial cell surface markers. Temporal analyses of the proteomes of the four populations revealed processes modulated during postnatal development and clarified the findings obtained from whole tissue proteome studies. Finally, the proteome was compared to a transcriptomics survey performed on the same lung samples to evaluate processes under post-transcriptional control.
Dataset ID LMEX0000004404
Assay Type Proteomics
Organism Human
Stages Neonate | Infant | Child
Sample Count 44
Sample Prep Lmdata:sample_type_sorted_cells
Technology Mass Spectrometry
External databases MassIVE: MSV000094189
FileDescriptionSize
log2-normalized-MS.xlsx
LungMAP IDAlt IDSpeciesSexRaceAgeAge GroupGA at BirthCGAWeightWeight PercentileCause of DeathType of Death
LMSP0000000131D008Homo sapiensFemaleWhite20 monthsChild12.25 kg86Trauma - Auto AccidentDBD (after brain death)
LMSP0000000134D011Homo sapiensFemaleWhite20 monthsChild40 weeks10.89 kg53Anoxic/Hypoxic Brain Injury - DrowningDBD (after brain death)
LMSP0000000141D018Homo sapiensFemaleWhite3 yearsChild15 kg73Anoxic/Hypoxic Brain Injury - DrowningDBD (after brain death)
LMSP0000000142D019Homo sapiensMaleWhite1 daysNeonate37 weeks, 3 days37.43 weeksCongenital Anomaly - BrainDCD (circulatory death)
LMSP0000000145D022Homo sapiensMaleOther2 yearsChild11.79 kg12Trauma - Isolated Head TraumaDBD (after brain death)
LMSP0000000035D024Homo sapiensMaleOther4 monthsInfant8.62 kg94Trauma - Auto AccidentDBD (after brain death)
LMSP0000000157D036Homo sapiensMaleWhite8 yearsChild34 kg89Trauma - Isolated Head TraumaDBD (after brain death)
LMSP0000000159D038Homo sapiensFemaleUnknown or Not Reported1 daysNeonate39 weeks, 3 days39.57 weeks2.27 kg1.2Congenital Anomaly - BrainDCD (circulatory death)
LMSP0000000162D041Homo sapiensMaleWhite6 daysNeonate38 weeks, 3 days39.14 weeks3.24 kg33Anoxic/Hypoxic Brain Injury - OtherDCD (circulatory death)
LMSP0000000164D043Homo sapiensMaleWhite21 monthsChild9.8 kg6.2Trauma - Isolated Head TraumaDBD (after brain death)
LMSP0000000165D044Homo sapiensMaleWhite6 daysNeonate40 weeks, 3 days41.57 weeks3.63 kg56Anoxic/Hypoxic Brain Injury - Neonatal HIEDCD (circulatory death)

11 of this study's 11 samples were also assayed by 317 other LungMAP studies, across 9 modalities. Click any node to list those studies.