Abstract
Regeneration is regulated not only by chemical signals but also by physical processes, such as bioelectric gradients. How these may change in the absence of the normal gravitational and geomagnetic fields is largely unknown. Planarian flatworms were moved to the International Space Station for 5 weeks, immediately after removing their heads and tails. A control group in spring water remained on Earth. No manipulation of the planaria occurred while they were in orbit, and space‐exposed worms were returned to our laboratory for analysis. One animal out of 15 regenerated into a double‐headed phenotype—normally an extremely rare event. Remarkably, amputating this double‐headed worm again, in plain water, resulted again in the double‐headed phenotype. Moreover, even when tested 20 months after return to Earth, the space‐exposed worms displayed significant quantitative differences in behavior and microbiome composition. These observations may have implications for human and animal space travelers, but could also elucidate how microgravity and hypomagnetic environments could be used to trigger desired morphological, neurological, physiological, and bacteriomic changes for various regenerative and bioengineering applications.
Highlights
Planarian flatworms are known for their mastery of regeneration (Reddien & Sanchez Alvarado, 2004; Sanchez Alvarado, 2003; Sheiman & Kreshchenko, 2015)
Our study examined how the regenerative and physiological properties of planaria changed during a space mission
Maintaining the temperature of control worms on Earth exactly the same as those samples that traveled to space during the entire space mission was more challenging than anticipated
Summary
Planarian flatworms are known for their mastery of regeneration (Reddien & Sanchez Alvarado, 2004; Sanchez Alvarado, 2003; Sheiman & Kreshchenko, 2015). Curiosity, and problem-solving abilities (Best & Rubenstein, 1962; Corning & Freed, 1968; McConnell, 1965; Pagán, 2014; Wells, 1967) They are able to repair and remodel three major polarity axes, dorsal/ventral, anterior/posterior, and medial/lateral, with outstanding accuracy (Gentile, Cebria, & Bartscherer, 2011; Gurley, Rink, & Alvarado, 2008; Kato, Orii, Watanabe, & Agata, 2001; Lange & Steele, 1978; Molina, Saló, & Cebrià, 2007; Orii & Watanabe, 2007; Owlarn & Bartscherer, 2016; Reddien, Bermange, Kicza, & Alvarado, 2007).
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