No abstract

The inferior colliculus (IC) represents a mid-brain structure which integrates information from many ascending auditory pathways, descending corticotectal projections and intercollicular pathways. The processing of information is different in each of the three main subdivisions of the IC--the central nucleus (CNIC), the dorsal cortex (DCIC) and the external cortex (ECIC)--which may be distinguished morphologically as well as by different inputs and outputs. To assess the differences in information processing we compared the response properties of single neurons in individual subnuclei of the IC in anesthetized guinea pigs. In comparison with DCIC and ECIC neurons, the CNIC neurons as a group were characterized by a sharper frequency tuning (as expressed by Q10 values), a lower average threshold, a shorter average first-spike latency of response to tones at the characteristic frequency (CF), a higher occurrence of non-monotonic rate/level functions and a higher rate of spontaneous activity. CNIC neurons and DCIC neurons reacted to tones at the CF more frequently by a sustained type of response than did ECIC neurons. The difference between the parameters of DCIC neuronal activity and ECIC neuronal activity was found to be smaller. The frequency tuning (expressed in Q10 values), spontaneous activity and dominance of monotonic rate/level functions were very similar in both structures; ECIC neurons expressed a higher average threshold and a shorter average first-spike latency than did DCIC neurons. Responsiveness expressed as the average maximal firing rate to tones at the CF was significantly higher in the CNIC than in the ECIC. The results give additional support to the idea that the CNIC is a part of a fast, frequency-tuned, low threshold and intensity-sensitive ascending pathway, whereas the other two subdivisions are involved in additional processing of information that involves feedback loops and polysensory pathways.

No abstract

Chromosomal rearrangements of NTRK genes are oncogenic driver mutations in thyroid cancer (TC). This study aimed to identify NTRK fusion-positive thyroid tumors and to correlate them with clinical and pathological data and determine their prognostic significance. The cohort consisted of 989 different TC samples. Based on the detected mutation, samples were triaged, and those that were positive for a BRAF, HRAS, KRAS, NRAS, RET, RET/PTC or PAX8/PPARγ mutation were excluded from further analyses. NTRK fusion gene testing was performed in 259 cases, including 126 cases using next-generation sequencing. NTRK fusion genes were detected in 57 of 846 (6.7%) papillary thyroid carcinomas and in 2 of 10 (20.0%) poorly differentiated thyroid carcinomas. A total of eight types of NTRK fusions were found, including ETV6/NTRK3, EML4/NTRK3, RBPMS/NTRK3, SQSTM1/NTRK3, TPM3/NTRK1, IRF2BP2/NTRK1, SQSTM1/NTRK1 and TPR/NTRK1.NTRK fusion-positive carcinomas were associated with the follicular growth pattern, chronic lymphocytic thyroiditis and lymph node metastases. NTRK1-rearranged carcinomas showed a higher frequency of multifocality and aggressivity than NTRK3-rearranged carcinomas. Tumor size, presence of metastases, positivity for the NTRK3 or NTRK1 fusion gene and a late mutation event (TERT or TP53 mutation) were determined as factors affecting patient prognosis. NTRK fusion genes are valuable diagnostic and prognostic markers.