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Biology subjects

Kabbara, S.

Publications and source records attributed to Kabbara, S..

2 recordsLinked to original sources

Lateral Propagation from Sensory Cortex Provides Differential Gain for Sensory Selection

Selectively responding to target stimuli while ignoring distractors is a fundamental cognitive ability. In neocortex, such selection is associated with enhanced responses to target stimuli relative to distractor stimuli, yet the gain mechanisms underlying this differential responsivity are poorly understood. Most proposed gain mechanisms emphasize modulation within the center response field of a stimulus. In contrast, here we investigate modulation of lateral propagation from the center response field as a potential gain mechanism during a whisker-based selective detection task in mice. Both target (Go) and distractor (NoGo) stimuli evoked activity that propagated beyond their center response fields, with substantially greater lateral propagation for target stimuli. Target-evoked propagation increased with task learning and, in expert mice, exhibited the spatiotemporal characteristics of a traveling cortical wave preferentially involving infragranular layers. Furthermore, we demonstrate that frontal cortex actively suppresses distractor-evoked sensory responses, including both center region activity and lateral cortical recruitment. Computational modeling showed that modulation of lateral excitation could reproduce key features of these experimental findings. Together, our results support the regulation of lateral cortical propagation as a mechanism for differentially amplifying behaviorally relevant sensory representations during sensory selection.

neuroscience↗

DNA damage induced during mitosis undergoes DNA repair synthesis

Understanding the mitotic DNA damage response (DDR) is critical to our comprehension of cancer, premature aging and developmental disorders which are marked by DNA repair deficiencies. In this study we use a micro-focused-laser to induce DNA damage in selected mitotic chromosomes to study the subsequent repair response. Our findings demonstrate that (1) mitotic cells are capable of DNA repair as evidenced by DNA synthesis at damage sites, (2) Repair is attenuated when DNA-PKcs and ATM are simultaneously compromised, (3) Laser damage may permit the observation of previously undetected DDR proteins when damage is elicited by other methods in mitosis, and (4) Twenty five percent of mitotic DNA-damaged cells undergo a subsequent mitosis. Together these findings suggest that mitotic DDR is more complex than previously thought and may involve factors from multiple repair pathways that are better understood in interphase.

cell biology↗