To address this gap, researchers used single-cell RNA sequencing to profile more than 44,000 cells obtained from autopsy testis samples from four young men and eight older men. The older donors were screened for having offspring as young adults to ensure early-adult fertility.
The young samples clustered together and did not display molecular signatures of aging or a disrupted ability to produce sperm cells.
Surprisingly, the older samples showed only modest age-related changes in stem cells that give rise to mature sperm but were classified into two distinct groups.
Advertisement
The first group displayed an intact ability to produce sperm cells, with only weak molecular signatures that distinguished them from young samples. By contrast, the second group showed a very limited ability to develop sperm cells.
Notably, BMI emerged as a critical factor among older individuals. All donors from the first group had levels lower than 27, whereas all donors from the second group had levels higher than 30.
Future Directions
Moving forward, larger patient cohorts are needed to fully validate the results. Another avenue for future research is to explore whether the testicular cells of older, heavy-set males show unique aging signatures, or whether they simply display accelerated aging.
It is also not clear whether diet, exercise, diabetes, or altered hormone production play a role in testis aging. In addition, determining at what age the dysregulation of supporting testis cells emerges, and whether and how it may be reversible, may lead to improved medical guidance for older men.
This research also serves as a foundational dataset for the scientific community to study how human testis and fertility respond to aging.
Source: Medindia
Source link
#Male #Fertility #Hard #Time #Aging #Heres
