Loe raamatut: «How to Build a Human: Adventures in How We Are Made and Who We Are»

INTRODUCTION
MY BRAIN IN A DISH

In the summer of 2017, a small piece of my arm was removed and turned into a rudimentary miniature brain. This book is my attempt to make sense of that strange experience.

On a hot day that July, I lay on a bed in the Institute of Neurology at University College London while neuroscientist Ross Paterson gouged a little chunk from my shoulder with a kind of miniature surgical apple-corer. A dab of local anaesthetic made it painless; to my great relief, there wasn’t much blood.

Bathed in a nutrient solution in a test-tube, that piece of my flesh was the seed for what, eight months later, would resemble a tiny brain.

It was my own “mini-brain”, a blob of neurons about the size of a lentil. They wired themselves into a dense network and could signal to one another in the way neurons do. I’m not going to say it was thinking; probably these signals were not much more than random sparks, incoherent noise, signifying nothing. But no one really knows how to think about what goes on inside a mini-brain, any more than they know what transpires in the formative brain of a fetus when it is of comparable pea-size.

This process of culturing new tissues from a piece of arm is not the way to create a human. But it could one day become a basis for doing that.

It’s not obvious why anyone, here and now, would think this a good idea. But the point is not that one day humans will, like the citizens of Aldous Huxley’s Brave New World, be cultivated from blobs of cells in the vats of some dystopian people-factory. The point is that such a vision is no longer obviously impossible. That alone should give us cause to revise our ideas about what we think we are. Having a piece of you grown into a mini-brain in an incubator five miles across town brings home to you, rather viscerally, why the need for that revision is upon us now.

My mini-brain under the microscope.

* * *

Let me explain.

My mini-brain was cultivated, nurtured and guided by neuroscientists Selina Wray and Christopher Lovejoy at UCL. That’s their job. They want to understand how brains develop, and in particular why some gene mutations send that process awry and trigger the onset of neurodegenerative diseases such as Alzheimer’s. These conditions, which many of us will confront – close to a million people in the UK are currently thought to be living with some form of dementia – are partly a consequence of ageing, but they can also have genetic roots. Some gene mutations confer particular susceptibility to dementias, and there are inheritable early-onset dementias that can affect people even in their thirties. My “brain in a dish” was grown as part of a large and ambitious project called Created Out of Mind, funded in 2016–18 by the Wellcome Trust to alter public perceptions of dementia and develop new tools for assessing the value of arts-based interventions for people living with these conditions.

Selina and Chris hope that, by studying the activity of genes in mini-brains cultured from the tissues of people with those genetic mutations, they might come to understand more about the causes, and ultimately find clues that could lead to possible cures. Scientists studying the genetic factors behind the neurodegenerative Huntington’s disease have already found that the baleful effect of one particular gene implicated in the condition can be tempered with drugs that intercept the conversion of the gene to a protein that is prone to “misfolding”. It’s this misfolded form that produces scarring and destruction of brain tissue. Others are working on vaccines that might prevent or remove the clumps of misfolded protein in the brain that seem to trigger Alzheimer’s itself.

To my knowledge, I do not have genes that make me susceptible to early-onset Alzheimer’s. But the aim of the Brains In A Dish project, coordinated by artist Charlie Murphy, was to explore and explain research like this through the response of its participants. Well, this book is mine.

I should be very clear what this term “mini-brain” implies. Some researchers reject it, and I see their point. Human neurons grown in a cell culture in this way can’t make a brain, not even in its early fetal form. But these nerve cells do start to create, under the direction of their own genetic programme, some of the features that a real developing brain exhibits. They become specialized into some of the many different cell types – not just neurons – that are found in our mature brains. And they acquire some of the anatomical structure of brains: the well-defined layers of neurons seen in the cortex, the folds and convolutions of the tissues. It’s rather like a very young child’s drawing of a person: not much of a resemblance really, but you can see what they’re getting at. You can see the potential to do a better job. A more neutral term for these lab-grown cell structures is “organoid”: the cells construct something that looks like a crude representation of an organ of the body, reduced in scale. It is possible to grow organoids resembling livers, kidneys, retinas, gut, as well as brains – all in a dish, outside the body. I want to ask what this means, for medicine, fundamental biology, philosophy and our sense of identity.

There was no rulebook to tell me how I should feel about my mini-brain. Certainly, I didn’t lie awake at night fretting over its welfare; this mass of tissue made from my skin didn’t take on the status of an individual. But I felt oddly fond of those cells, doing their best to fulfil a role in the absence of the guiding influence of their somatic source.¹ There was a curious intimacy involved, a sense of potential that wasn’t present initially in the tiny chunk of arm-flesh excised and placed in a test-tube. This was more than a matter of cells subsisting; this was life in all its teeming, multiplying glory, spilling out from a paring of me.

My skin cells (fibroblasts) growing in a petri dish (in vitro) from a piece of skin tissue taken from my arm.

It’s hard not to invest the whole of biology with intentions, purposes, wants and needs, even though cells and simple organisms resemble automata responding without volition to the signals from their environment. (Some would say this applies to humans too.) That’s just how nature works.

Yet seeing these cells do their business in a petri dish is to recognize that life exists in doing. It is a process in which change is the only constant: change imbued with direction, more or less constrained onto a trajectory that evolution has guided and given what looks almost indistinguishable from a purpose, until death makes that change an inexorable slide into decay and entropic dissolution. There is no agreed scientific definition of “life”, but such a thing (if it is possible at all) would mean little if it fails to acknowledge this dynamic aspect, this interplay of predetermined pattern and historical contingency. It feels banal to say that my excised cells took on a life of their own, but what is so new and so remarkable about the science behind organoids is that we have the knowledge and power to influence the direction that life takes.

* * *

What really needs explaining is that my mini-brain was grown from a piece of my arm: in essence, from skin cells. That doesn’t sound like something that should be possible. Until barely more than a decade ago, most biologists thought so too. The discoveries that changed this view have transformed cell biology, raising all manner of medical possibilities for regenerating organs and tissues as well as opening up new avenues for basic research into embryology, development and conception. These discoveries and their applications are at the heart of this book.

But although these cell-transforming technologies have been celebrated, sometimes in breathless and hyperbolic terms, in the popular press, I’m not at all sure that their wider philosophical, one might even say psychic, implications have been acknowledged. Here is one of the profound things they say to us:

Every part of ourselves can potentially be turned into any other part of ourselves – including a complete self.

This, let me add, is more than science has yet proved. There is some small print attached, and further ingredients might be needed to fulfil the last part of the bargain. All the same, we are more plastic than we ever guessed. And that realization is in turn a culmination of medical advances and discoveries that have taken place over the course of the past century, which too we have processed only in the manner that we always process discoveries we don’t know how to think about. That’s to say, we have framed it around fears, fantasies and fiction.

For example: perhaps my “brain in a dish” immediately invokes visions of Frankenstein. And I pointed you also towards Brave New World, that re-envisioning of Mary Shelley’s tale for the age of industrialization and mass culture. These two novels remain today the favourite, off-the-shelf points of cultural reference for biomedical advances that unsettle and boggle the mind. But we are sent back to other speculative fictions by some of the possibilities that I have seen seriously and soberly discussed in the context of cell transformation and organoid growth. For example:

 It may well be possible to grow a human brain in the body of a pig. One reason I find this so disturbing is that I still vividly remember first seeing the scene in Lindsay Anderson’s 1973 film, O Lucky Man!, where … well, if you don’t know it already, don’t let me spoil it for you.

 It might be feasible to grow each organ of the human body separately outside the body itself in some sort of vessel (in vitro), and then surgically assemble them into a person – or enough of a person to be, let’s say, a personoid. And this is precisely how the first robots were made, in Karel Čapek’s 1921 play, R.U.R.

 Philosophers, ethicists and neuroscientists are now compelled to debate what it could mean to create a full-grown human brain in a vat. Could it be conscious? Would it experience a self-contained interior “reality”? The pop-culture reference point here, which philosophers have embraced with nerdy delight, is of course the Matrix movies of the Wachowskis.

Let me make it clear that no researcher sees any prospect of these things happening in the near future, nor any good reason to try to make them happen. I will look at them more closely later, but my point here is not to tell rather shocking and thrillingly grotesque scare stories in a bout of bait-and-switch. What matters is that, confronted with so disorienting and disturbing a set of imaginable possibilities, we seem to need such stories in order to frame our thoughts. That in itself is worth considering. What motivates and shapes these narratives?

Underpinning them, I believe, is a consideration that might at first strike you as odd: We are not at ease with our own flesh.

But surely, you might say, we inhabit our own flesh? I’m putting those words into your mouth because they have a familiar ring to them – it doesn’t seem a strange thing to suggest. Yet such a phrase serves more to disassociate than to unite us with our flesh. We inhabit it? Like a person who inhabits a house? So what, then, are “we”? It’s the old Cartesian dualism: the separation of mind and body, or as some might have once said, of body and soul.

Yet of course we are not at ease in our own flesh! How we recoil from its routine functions, its excrescences and smells and fluids. How hard we try to remodel it, with what horror we watch its decrepitude. How we flock to watch movies like Hellraiser and Saw, or, at the more sophisticated end of the body-horror market, pretty much any of David Cronenberg’s early oeuvre. Gunther von Hagens, with his plasticized corpses, has made a career from an artful exploration of our horrified fascination; artists from Mark Quinn (who has sculpted with his own blood and the placenta of his baby son) to Marina Abramović have made what are often brave, painful and stomach-churning attempts to help us engage with our raw material.

There are many reasons for this ambivalence towards the somatic aspects of human existence, expressed repeatedly in all cultures in all ages: with piercings and tattoos, rituals of embalming and burial, elaborate taboos and the normative strictures of surgery. But the new sciences of culturing and transforming our cellular fabric confront us with perhaps the most fundamental challenge for our relationship with our flesh. They show us the ultimate in dismemberment: a reduction of the person to the cell.

Time was when we could dismiss that. Sure, cells are our building blocks, but no more or less so than proteins, atoms or quarks. If a chunk of our cellular material were removed, well, so what? It was no longer “us”, but a piece of waste, separate and dead, soon to be putrescent and doomed by microbes and entropy.

Having your skin grown into neurons that assemble themselves into a brain organoid is a pretty convincing way to find out how obsolete that notion is. All the more so when you see it through the microscope and realize that this is not merely some trick of preservation. Life on that scale is multitudinous, and thriving, and it has a plan of sorts.

Life? Whose life?

Not mine, exactly – and yet who else’s can it be? Those cells are autonomous – but why any more so than the cells still in my arm, in my real brain (the need for that specifying adjective still makes me blink), my surging blood and beating heart? And so I come by degrees to accept the inevitable truth: I am a colony of cells, whose cooperation lets me draw breath, whose communication produces my sense of identity and uniqueness.

That is what is fundamentally disconcerting about our own flesh. It grew as a colony from a single cell, and we’re not quite sure where (or when) in this teeming morass to pin the label “me”.

The new cell technologies are making it impossible for us any longer to ignore this fact. I won’t pretend that I know how to normalize it, but I think there is a strange kind of liberation that can come from letting ourselves be unsettled by it.