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| Status |
Public on Oct 06, 2020 |
| Title |
Expression data of CD107aLow and CD107aHigh cells isolated from human adipose tissue |
| Organism |
Homo sapiens |
| Experiment type |
Expression profiling by high throughput sequencing
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| Summary |
The tunica adventitia of vessels within adipose tissue (AT) represents a heterogenous microanatomical niche for multipotent mesenchymal precursor cells. To investigate this heterogeneity, cell surface antibody array among CD34+ human adventicytes identified 13 novel antigens enriched within perivascular mesenchyme, including the endolysomal associated protein CD107a (LAMP1). Membranous CD107a can be used to divide perivascular / adventitial precursor cells into functional relevant subsets. CD107alow cells from human AT demonstrated high colony forming efficiency, osteoprogenitor cell frequency, and osteogenic potential. Conversely, CD107ahigh cells demonstrated heightened adipoprogenitor cell frequency and adipogenic potential. Knockdown experiments did not identity a functional role for CD107a in osteo/adipogenic differentiation. Instead, CD107a protein trafficking to the cell surface was associated with exocytosis during early adipogenic differentiation. Bulk and single cell RNA Sequencing suggested that CD107alow cells represent a precursor population for CD107ahigh cells. Functional roles for CD107alow/high subsets were confirmed in transplantation experiments. Intramuscular transplantation of CD107alow cells yielded increased bone formation in comparison to their CD107ahigh counterparts. Further, CD107alow cells induced spine fusion whereas their CD107ahigh counterparts did not. In sum, cell surface CD107a in mesenchymal progenitors correlates with exocytosis during early adipogenesis, and can be used to divide osteo- from adipogenic progenitor cells within human fat tissue.
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| Overall design |
6 Total samples were analyzed: 3 CD107aHigh biological replicates and three CD107aLow controls as determined by FACS.
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| Contributor(s) |
James A, Xu J |
| Citation(s) |
33044169 |
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| Submission date |
Apr 12, 2020 |
| Last update date |
Jan 05, 2021 |
| Contact name |
Aaron W James, MD, PhD |
| Organization name |
Johns Hopkins University School of Medicine
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| Department |
Pathology
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| Lab |
Ross 524
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| Street address |
600 North Wolfe Street
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| City |
Baltimore |
| State/province |
MD |
| ZIP/Postal code |
21287 |
| Country |
USA |
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| Platforms (1) |
| GPL18573 |
Illumina NextSeq 500 (Homo sapiens) |
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| Samples (6)
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| Relations |
| BioProject |
PRJNA624864 |
| SRA |
SRP256240 |
| Supplementary file |
Size |
Download |
File type/resource |
| GSE148519_JXu-107a-LogQuant-Signals.txt.gz |
561.9 Kb |
(ftp)(http) |
TXT |
SRA Run Selector |
| Raw data are available in SRA |
| Processed data are available on Series record |
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