Spatial Transcriptomics Analysis: Maternal Obesity Impairs Myogenic Cell Migration and Differentiation during Embryonic Limb Development.
Yao GaoMd Nazmul HossainLiang ZhaoJeanene Marie DeavilaNathan C LawMei-Jun ZhuGordon K MurdochMin DuPublished in: International journal of molecular sciences (2024)
Limb muscle is responsible for physical activities and myogenic cell migration during embryogenesis is indispensable for limb muscle formation. Maternal obesity (MO) impairs prenatal skeletal muscle development, but the effects of MO on myogenic cell migration remain to be examined. C57BL/6 mice embryos were collected at E13.5. The GeoMx DSP platform was used to customize five regions along myogenic cell migration routes (myotome, dorsal/ventral limb, limb stroma, limb tip), and data were analyzed by GeomxTools 3.6.0. A total of 2224 genes were down-regulated in the MO group. The GO enrichment analysis showed that MO inhibited migration-related biological processes. The signaling pathways guiding myogenic migration such as hepatocyte growth factor signaling, fibroblast growth factor signaling, Wnt signaling and GTPase signaling were down-regulated in the MO E13.5 limb tip. Correspondingly, the expression levels of genes involved in myogenic cell migration, such as Pax3 , Gab1 , Pxn , Tln2 and Arpc , were decreased in the MO group, especially in the dorsal and ventral sides of the limb. Additionally, myogenic differentiation-related genes were down-regulated in the MO limb. MO impedes myogenic cell migration and differentiation in the embryonic limb, providing an explanation for the impairment of fetal muscle development and offspring muscle function due to MO.
Keyphrases
- cell migration
- skeletal muscle
- insulin resistance
- growth factor
- spinal cord
- metabolic syndrome
- transcription factor
- type diabetes
- adipose tissue
- physical activity
- high fat diet
- neuropathic pain
- pregnant women
- body mass index
- spinal cord injury
- cell proliferation
- deep brain stimulation
- artificial intelligence
- endoplasmic reticulum stress
- bioinformatics analysis