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Knappe, S.

Publications and source records attributed to Knappe, S..

2 recordsLinked to original sources

Measurement Equivalence of On-Scalp OPM-MEG and Cryogenic MEG for Auditory and Somatosensory Cortical Mapping Across Development

Wearable optically pumped magnetometer magnetoencephalography (OPM-MEG) reduces sensor-to-cortex distance compared with conventional cryogenic SQUID-MEG, but whether the two technologies yield equivalent neurophysiological conclusions remains unclear. We recorded auditory and somatosensory evoked fields in 18 participants (10-45 years) using a 128-sensor FieldLine HEDscan OPM-MEG system and a 275-channel CTF SQUID-MEG system within the same individuals. Equivalent current dipole source models were estimated using identical preprocessing and modeling procedures and compared using paired permutation testing. Both systems localized canonical auditory and somatosensory cortical generators with matched peak latencies and modest cross-system spatial differences. Auditory sources showed a consistent medial bias in SQUID-MEG localization, whereas somatosensory sources exhibited a small systematic offset ([~]4 mm), indicating stable coordinate differences rather than localization error. Dipole moments were larger for SQUID-MEG and goodness-of-fit higher for OPM-MEG; however, the increased moment was explained by a medial localization bias, demonstrating inverse-model effects rather than physiological disagreement. Auditory dipole moment increased with age in both systems, whereas somatosensory responses showed no age-related change. Together, these observations indicate preserved developmental physiology across platforms. These findings demonstrate that OPM-MEG and SQUID-MEG recover the same cortical generators and support equivalent biological interpretations despite predictable geometry-dependent coordinate differences. OPM-MEG therefore represents a measurement-equivalent implementation of MEG suitable for sensory functional mapping.

neuroscience↗

Myotome adaptability confers developmental robustness to somitic myogenesis in response to fibre number alteration.

Summary StatementHomeostatic interactions between muscle stem cells and fibres during myogenesis ensure the correct muscle size is formed independent of fibre number in zebrafish\n\nAbstractBalancing the number of stem cells and their progeny is crucial for tissue development and repair. Here we examine how muscle stem/precursor cell (MPC) numbers are tightly regulated during zebrafish somitic muscle development. MPCs expressing Pax7 are initially located in the dermomyotome (DM) external cell layer, adopt a highly stereotypical distribution and thereafter a proportion of MPCs migrate into the myotome. Regional variations in the proliferation and terminal differentiation of MPCs contribute to growth of the myotome. To probe the robustness of spatiotemporal regulation of MPCs, we compared the behaviour of wild type (wt) MPCs with those in mutant zebrafish that lack the muscle regulatory factor Myod. Myodfh261 mutants form one third fewer multinucleate fast muscle fibres than wt and show a significant expansion of the Pax7+ MPC population in the DM. Subsequently, myodfh261 mutant fibres generate more cytoplasm per nucleus, leading to recovery of muscle bulk. In addition, relative to wt siblings, there is an increased number of MPCs in myodfh261 mutants and these migrate prematurely into the myotome, differentiate and contribute to the hypertrophy of existing fibres. Thus, homeostatic reduction of the excess MPCs returns their number to normal levels, but fibre numbers remain low. The GSK3 antagonist BIO prevents MPC migration into the deep myotome, suggesting that canonical Wnt pathway activation maintains the DM in zebrafish, as in amniotes. BIO does not, however, block recovery of the myodfh261 mutant myotome, indicating that homeostasis acts on fibre intrinsic growth to maintain muscle bulk. The findings suggest the existence of a critical window for early fast fibre formation followed by a period in which homeostatic mechanisms regulate myotome growth by controlling fibre size.

developmental biology↗