This study investigates how caffeine intake affects blood stem and progenitor cells in healthy adults. The trial will compare people who regularly consume caffeine with those who consume very little or none. All participants will receive a single 200 mg caffeine tablet (similar to one cup of coffee) under fasting conditions. Blood samples will be collected before and three hours after caffeine intake. The study will assess whether caffeine influences the mobilization of blood stem and progenitor cells from the bone marrow into the bloodstream. It will also examine the effects of caffeine on the function, gene activity, and metabolism of blood cells.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
100
Participants receive a single oral dose of 200 mg caffeine under fasting conditions. Blood samples are collected before and three hours after intake to evaluate effects on hematopoietic stem and progenitor cells, including mobilization, function, gene expression, and metabolism.
ETH GLC
Zurich, Canton of Zurich, Switzerland
Mobilization of hematopoietic stem and progenitor cells
The change in the numbers of mobilized HSPCs (defined as CD34+ cells) \[cells/ml\] in blood (measured by flow cytometry) from baseline to three hours after intake of a single oral dose of 200mg caffeine in habitual caffeine consumers versus non-caffeine consumers.
Time frame: From baseline to three hours after caffeine intake
Mobilization of hematopoietic stem and progenitor cells
The change in the relative abundance of HSPCs \[% HSPCs of total PBMCs\] in blood (measured by flow cytometry) from baseline to three hours after intake of a single oral dose of 200mg caffeine in habitual caffeine consumers versus non-caffeine consumers.
Time frame: From baseline to three hours after caffeine intake
Functional alterations in CD34+ peripheral blood cells
Functional alterations in CD34+ PB cells: self-renewal \[number of colonies\] assessed via colony-forming unit assay.
Time frame: From baseline to three hours after caffeine intake
Functional alterations in CD34+ peripheral blood cells
Functional alterations in CD34+ PB cells: single HSPC proliferation \[number of cell divisions within 72h\] assessed via single HSC proliferation assay.
Time frame: From baseline to three hours after caffeine intake
Transcriptional changes in CD34+ cells
Transcriptional changes in CD34+ cells \[log2 fold change in gene expression and DEG count\] assessed via single-cell RNA sequencing.
Time frame: From baseline to three hours after caffeine intake
Relative metabolite abundance
Relative metabolite abundance \[arbitrary units based on peak area or height in LC-MS\] in plasma and intracellularly in isolated CD34+ cells.
Time frame: From baseline to three hours after caffeine intake
Change in the numbers of peripheral blood cells
The change in the numbers of PB cells \[cells/ml\], including B cells, T cells, myeloid cells in blood, and relative, and measured by flow cytometry
Time frame: From baseline to three hours after caffeine intake
Change in the numbers of peripheral blood cells
The change in relative abundance of PB cells \[% cell type of total PBMCs\] including B cells, T cells, myeloid cells in blood, and measured by flow cytometry
Time frame: From baseline to three hours after caffeine intake
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