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1.
Genes Brain Behav ; 19(4): e12638, 2020 04.
Article in English | MEDLINE | ID: mdl-31943801

ABSTRACT

Salient sensory environments experienced by a parental generation can exert intergenerational influences on offspring. While these data provide an exciting new perspective on biological inheritance, questions remain about causes and consequences of intergenerational influences of salient sensory experience. We previously showed that exposing male mice to a salient olfactory experience, like olfactory fear conditioning, resulted in offspring demonstrating a sensitivity to the odor used to condition the paternal generation and possessing enhanced neuroanatomical representation for that odor. In this study, we first injected RNA extracted from sperm of male mice that underwent olfactory fear conditioning into naïve single-cell zygotes and found that adults that developed from these embryos had increased sensitivity and enhanced neuroanatomical representation for the odor (Odor A) with which the paternal male had been conditioned. Next, we found that female, but not male offspring sired by males conditioned with Odor A show enhanced consolidation of a weak single-trial Odor A + shock fear conditioning protocol. Our data provide evidence that RNA found in the paternal germline after exposure to salient sensory experiences can contribute to intergenerational influences of such experiences, and that such intergenerational influences confer an element of adaptation to the offspring. In so doing, our study of intergenerational influences of parental sensory experience adds to existing literature on intergenerational influences of parental exposures to stress and dietary manipulations and suggests that some causes (sperm RNA) and consequences (behavioral flexibility) of intergenerational influences of parental experiences may be conserved across a variety of parental experiences.


Subject(s)
Olfactory Perception/genetics , Animals , Female , Male , Mice , Mice, Inbred C57BL , Pedigree , RNA/genetics , RNA/metabolism , Spermatozoa/metabolism , Zygote/metabolism
2.
Biol Psychiatry ; 85(3): 248-256, 2019 02 01.
Article in English | MEDLINE | ID: mdl-30292395

ABSTRACT

BACKGROUND: Stressors affect populations exposed to them as well as offspring. Strategies preventing the intergenerational propagation of effects of stress would benefit public health. Olfactory cue-based fear conditioning provides a framework to address this issue. METHODS: We 1) exposed adult male mice to an odor, acetophenone (Ace) or Lyral (parental generation [F0]-Exposed), 2) trained mice to associate these odors with mild foot shocks (F0-Trained), and 3) trained mice to associate these odors with mild foot shocks and then extinguished their fear toward these odors with odor-only presentations (F0-Extinguished). We then examined sensitivity of future generation (F1) offspring to these odors, expression of M71 odorant (Ace-responsive) and MOR23 odorant (Lyral-responsive) receptor-expressing cell populations in F1 offspring, and DNA methylation at genes encoding the Ace- (Olfr151, Olfr160) and Lyral- (Olfr16) responsive receptors in F0 sperm. RESULTS: Extinguishing fear toward Ace or Lyral of F0 male mice (F0-Extinguished) that had been fear conditioned with Ace or Lyral, respectively, results in F1-Extinguished offspring that do not demonstrate behavioral sensitivity to Ace or Lyral, respectively, and do not have enhanced representation for M71 or MOR23 odorant receptors in the olfactory system, as is observed in F1-Trained-Ace or F1-Trained-Lyral cohorts, respectively. The promoters of genes encoding Olfr151 and Olfr160 receptors are less methylated in F0-Trained-Ace sperm compared with F0-Exposed-Ace sperm. The Olfr16 promoter is less methylated in F0-Trained-Lyral sperm compared with F0-Exposed-Lyral sperm, and F0-Extinguished-Lyral sperm have methylation levels comparable to F0-Exposed-Lyral sperm. CONCLUSIONS: Our study demonstrates the potential of using extinction-based behavioral strategies to reverse influences of parental stress in offspring and in the parental germline.


Subject(s)
Child of Impaired Parents/psychology , DNA Methylation , Stress, Psychological/genetics , Stress, Psychological/pathology , Acetophenones/pharmacology , Aldehydes/pharmacology , Animals , Conditioning, Classical , Cyclohexenes/pharmacology , Extinction, Psychological , Fear , Female , Germ Cells , Male , Mice , Mice, Transgenic , Receptors, Odorant/biosynthesis , Receptors, Odorant/metabolism , Spermatozoa/metabolism
3.
Neuron ; 95(1): 169-179.e3, 2017 Jul 05.
Article in English | MEDLINE | ID: mdl-28648500

ABSTRACT

Lattice-like structures known as perineuronal nets (PNNs) are key components of the extracellular matrix (ECM). Once fully crystallized by adulthood, they are largely stable throughout life. Contrary to previous reports that PNNs inhibit processes involving plasticity, here we report that the dynamic regulation of PNN expression in the adult auditory cortex is vital for fear learning and consolidation in response to pure tones. Specifically, after first confirming the necessity of auditory cortical activity for fear learning and consolidation, we observed that mRNA levels of key proteoglycan components of PNNs were enhanced 4 hr after fear conditioning but were no longer different from the control groups 24 hr later. A similar pattern of regulation was observed in numbers of cells surrounded by PNNs and area occupied by them in the auditory cortex. Finally, the removal of auditory cortex PNNs resulted in a deficit in fear learning and consolidation.


Subject(s)
Auditory Cortex/metabolism , Conditioning, Psychological/physiology , Extracellular Matrix/metabolism , Fear/physiology , Learning/physiology , Proteoglycans/genetics , Animals , Auditory Cortex/drug effects , Auditory Cortex/physiology , Conditioning, Psychological/drug effects , Extracellular Matrix/physiology , Fear/drug effects , GABA-A Receptor Agonists/pharmacology , Learning/drug effects , Memory Consolidation/drug effects , Memory Consolidation/physiology , Mice , Muscimol/pharmacology , Proteoglycans/metabolism , RNA, Messenger/metabolism
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