Human monocyte subtype expression of neuroinflammation and regeneration-related genes is linked to age and sex.
Juliane F TampéEmanuela MonniSara Palma-TortosaEmil BrogårdhCharlotta BoiersArne G LindgrenZaal KokaiaPublished in: bioRxiv : the preprint server for biology (2024)
Stroke is a leading cause of disability and the third cause of death. The immune system plays an essential role in post-stroke recovery. After an ischemic stroke, monocytes infiltrate the injured brain tissue and can exacerbate or mitigate the damage. Ischemic stroke is more prevalent in the aged population, and the aging brain exhibits an altered immune response. There are also sex disparities in ischemic stroke incidence, outcomes, and recovery, and these differences may be hormone-driven and determined by genetic and epigenetic factors. Here, we studied whether human peripheral blood monocyte subtype (classical, intermediate, and non-classical) expression of neuronal inflammation- and regeneration-related genes depends on age and sex. A FACS analysis of blood samples from 44 volunteers (male and female, aged 28 to 98) showed that in contrast to other immune cells, the proportion of natural killer cells increased in females. The proportion of B-cells decreased in both sexes with age, and subtypes of monocytes were not linked to age or sex. Gene expression analysis by qPCR identified several genes differentially correlating with age and sex within different monocyte subtypes. Interestingly, ANXA1 and CD36 showed a consistent increase with aging in all monocytes, specifically in intermediate ( CD36 ) and intermediate and non-classical ( ANXA1 ) subtypes. Other genes ( IL-1β, S100A8, TNFα, CD64, CD33, TGFβ1, TLR8, CD91 ) were differentially changed in monocyte subtypes with increased aging. Most age-dependent gene changes were differentially expressed in female monocytes. Our data shed light on the nuanced interplay of age and sex in shaping the expression of inflammation- and regeneration-related genes within distinct monocyte subtypes. Understanding these dynamics could pave the way for targeted interventions and personalized approaches in post-stroke care, particularly for the aging population and individuals of different sexes.
Keyphrases
- peripheral blood
- dendritic cells
- endothelial cells
- immune response
- poor prognosis
- genome wide
- atrial fibrillation
- stem cells
- oxidative stress
- genome wide identification
- healthcare
- multiple sclerosis
- dna methylation
- rheumatoid arthritis
- copy number
- magnetic resonance imaging
- physical activity
- cerebral ischemia
- binding protein
- resting state
- natural killer cells
- type diabetes
- machine learning
- gene expression
- functional connectivity
- cancer therapy
- skeletal muscle
- cognitive impairment
- lps induced
- metabolic syndrome
- insulin resistance
- palliative care
- drug delivery
- lipopolysaccharide induced
- brain injury
- pain management
- big data
- nuclear factor
- affordable care act
- blood brain barrier
- quality improvement