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RESEARCH PAPER / 2024-04-09

Overexpression of α-Klotho isoforms promotes distinct Effects on BDNF-Induced Alterations in Dendritic Morphology.

Marina Minto Cararo-Lopes, Ratchell Sadovnik, Allen Fu, Shradha Suresh, Srinivasa Gandu, Bonnie L Firestein

Department of Cell Biology and Neuroscience, Rutgers, The State University of New Jersey, Piscataway, NJ, USA.Department of Cell Biology and Neuroscience, Rutgers, The State University of New Jersey, Piscataway, NJ, USA. · pubmed

Abstract

α-Klotho (α-Kl) is a modulator of aging, neuroprotection, and cognition. Transcription of the Klotho gene produces two splice variants-a membrane protein (mKl), which can be cleaved and released into the extracellular milieu, and a truncated secreted form (sKl). Despite mounting evidence supporting a role for α-Kl in brain function, the specific roles of α-Kl isoforms in neuronal development remain elusive. Here, we examined α-Kl protein levels in rat brain and observed region-specific expression in the adult that differs between isoforms. In the developing hippocampus, levels of isoforms decrease after the third postnatal week, marking the end of the critical period for development. We overexpressed α-Kl isoforms in primary cultures of rat cortical neurons and evaluated effects on brain-derived neurotrophic factor (BDNF) signaling. Overexpression of either isoform attenuated BDNF-mediated signaling and reduced intracellular Ca

The following analysis is generated by AI and may contain errors. It is separate from the authors’ abstract and is not peer review.

Research summary

The paper investigates the role of α-Klotho isoforms in neuronal development and their effects on BDNF signaling, which are relevant to neuroprotection and cognitive function in the context of aging. However, the focus is primarily on the mechanisms of neuronal signaling rather than addressing the root causes of aging or lifespan extension. The findings contribute to understanding the molecular underpinnings of neurobiology but do not present a significant breakthrough or transformative implications for longevity research.

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